Best EMC Laboratory & Testing Labs for Medical Devices

Q: What is an EMC laboratory and what do they test?

An EMC laboratory (also called emc lab , electromagnetic compatibility laboratory , or emc testing lab ) is an accredited testing facility that performs electromagnetic compatibility testing on medical devices and other electronic equipment. EMC laboratories test two main areas: emissions (how much electromagnetic energy your device emits) and immunity (how well your device functions when exposed to electromagnetic disturbances). For medical devices, emc testing labs typically test to IEC 60601-1-2 [1] . Many EMC laboratories also offer electrical safety testing (IEC 60601-1) and are accredited to ISO/IEC 17025 [2] . When searching for 'emc labs near me' or 'emc testing labs near me', verify the laboratory's accreditation scope covers your specific testing needs.

Q: What is the difference between IEC 60601-1 and IEC 60601-1-2?

IEC 60601-1 addresses electrical safety and essential performance requirements for medical electrical equipment [1] , including protection against electrical hazards, mechanical safety, and risk management. IEC 60601-1-2 addresses electromagnetic compatibility (EMC) [2] , including emissions (how much electromagnetic energy the device emits) and immunity (how well the device functions in the presence of electromagnetic disturbances). Most medical electrical equipment requires testing to both standards at an accredited EMC laboratory or electrical safety testing lab for regulatory compliance.

Q: What is the difference between an EMC lab and an EMI testing lab?

EMC (Electromagnetic Compatibility) and EMI (Electromagnetic Interference) are closely related terms. An EMI testing lab typically focuses on measuring electromagnetic interference/emissions from devices, while an EMC laboratory or emc test laboratory performs both emissions testing and immunity testing (how devices respond to electromagnetic disturbances). For medical devices, most emc test houses and electromagnetic compatibility laboratories offer comprehensive testing to IEC 60601-1-2 [1] , which includes both EMI/emissions and immunity requirements. When requesting quotes, clarify whether you need emissions only, immunity only, or complete EMC testing. Most accredited emc testing labs offer full-service testing packages.

Q: Do I need both safety and EMC testing, or can I do just one?

Most medical electrical equipment requires both safety (IEC 60601-1) [1] and EMC (IEC 60601-1-2) [2] testing for regulatory compliance. However, some emc laboratories and electrical safety testing labs offer testing to individual standards if you only need one. For example, if you've already completed safety testing elsewhere, you might only need EMC testing at an emc test laboratory. Confirm with your regulatory team and target markets which tests are required. Most emc testing labs offer package deals for complete testing (safety + EMC) that are more cost-effective than separate testing.

Q: What is ISO/IEC 17025 accreditation and why does it matter?

ISO/IEC 17025 is the international standard for testing and calibration laboratory competence [1] . Accreditation to ISO/IEC 17025 demonstrates that an EMC laboratory, electrical safety testing lab, or emc test laboratory has the technical competence, quality management system, and measurement traceability to perform specific tests reliably. Accredited test reports from emc testing labs are generally required for regulatory submissions in most markets (FDA 510(k), CE marking, etc.). When requesting quotes from emc laboratories or electrical safety testing labs, ask for their accreditation scope document to verify they're accredited for your specific standards and test methods (IEC 60601-1, IEC 60601-1-2, etc.).

Q: How long does IEC 60601 testing typically take?

Testing timelines vary based on device complexity, test scope, and laboratory capacity. Typical timelines: EMC testing only: 3-4 weeks from sample receipt; Safety testing only: 4-6 weeks; Complete package (Safety + EMC): 6-10 weeks. Rush services (2-4 weeks) are available at most laboratories but typically cost 20-50% more. Factors affecting timeline include: device complexity (more test configurations = longer testing), retest needs (if initial tests reveal issues), laboratory backlog, and report preparation time. Plan for 8-12 weeks total project time (including sample shipping, testing, and report delivery) for standard lead times.

Q: What is pre-scan/debugging and do I need it?

Pre-scan/debugging is optional early-stage EMC testing performed before formal compliance testing. It helps identify EMC issues (emissions or immunity problems) early, allowing you to fix them before expensive formal testing. Pre-scan services are particularly valuable if: you're new to EMC testing, you've had EMC issues in the past, your device has complex electronics or wireless capabilities, or you want to reduce the risk of retesting. While pre-scan adds to project cost, it can save significant time and money by avoiding retests. Many laboratories offer pre-scan as an optional service.

Q: Can I use the same test report for FDA 510(k) and CE marking?

In many cases, yes — test reports from accredited laboratories testing to IEC 60601-1 and IEC 60601-1-2 [1] [2] are generally accepted by both FDA (for 510(k) submissions) [3] and EU notified bodies (for CE marking under MDR) [4] . However, confirm with your regulatory team and testing laboratory, as some markets may have specific requirements or test method variations. Accredited test reports from ISO/IEC 17025-accredited laboratories [5] are typically the most widely accepted.

Q: What if my device fails testing?

If your device fails initial testing, most laboratories offer retest support and engineering consultation to help identify and fix issues. Common failure modes include: EMC emissions exceeding limits (requiring shielding or filtering), EMC immunity failures (requiring better circuit design or protection), or safety issues (requiring design changes). Laboratories typically provide detailed failure analysis and recommendations. You'll need to: fix the issues, potentially retest specific areas, and pay for retesting (usually at a reduced rate). Pre-scan/debugging services can help identify issues early and reduce the risk of formal test failures.

Q: Do I need IEC 60601-1-11 testing for home-use devices?

If your medical electrical equipment is intended for use in the home healthcare environment , you may need additional testing per IEC 60601-1-11 [1] . This collateral standard addresses specific safety and performance requirements for devices used by lay users in non-clinical environments. Requirements include: usability considerations, environmental conditions (temperature, humidity, power quality variations), and instructions for use. Confirm with your regulatory team and testing laboratory whether IEC 60601-1-11 applies to your device. Many laboratories offer IEC 60601-1-11 testing as an add-on service.

Compare accredited EMC laboratories and electrical safety testing labs for IEC 60601-1 and IEC 60601-1-2 compliance. Find EMI testing labs, electromagnetic compatibility laboratories, and emc test houses near you. Request quotes, review capabilities, and choose an accredited lab for your regulatory submission needs.

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Compare Electrical Safety + EMC Testing (IEC 60601) Providers

For the most complete service details (including category-specific capabilities and requirements), open any provider profile below. Each profile contains full coverage, service details, and a direct quote request flow.

UL Solutions

UL Solutions is a global safety science leader providing testing, certification, and advisory services for medical device EMC, hazardous locations, and more. They help ensure product safety, regulatory compliance, and market access worldwide.

UL Solutions is a premier global safety science leader dedicated to helping companies navigate complex regulatory landscapes and achieve market access. Specializing in areas critical to the medical device industry, they offer comprehensive Electromagnetic Compatibility (EMC) testing and certification services. This includes addressing susceptibility to and immunity from electromagnetic disturbances, crucial for medical technology advancements. Beyond EMC, UL Solutions provides extensive expertise in Hazardous Locations (HazLoc) compliance, offering advisory, auditing, testing, and certification verification. They help manufacturers obtain necessary credentials for global markets, including certifications like UL, C-UL, ATEX, IECEx, and others. Their global network of experts and state-of-the-art facilities ensures products meet local regulations and gain acceptance from EPCs, end-users, and code authorities. UL Solutions' broader service portfolio encompasses testing, certification, auditing, and advisory services across various domains. They leverage their deep expertise and global reach to accelerate product development, enhance security, and ensure compliance with international standards. By partnering with UL Solutions, companies can mitigate risks, demonstrate product quality and safety, and build trust in the global marketplace, ultimately achieving key business objectives and contributing to a safer, more secure, and sustainable world.

Website: ul.com

HQ: US

Languages: English

Standards: IEC 60601-1-2

Test Coverage: Both

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Intertek

Intertek offers specialized EMC testing for medical devices. They provide expert services to ensure your products meet regulatory standards for electromagnetic compatibility.

Intertek is a global leader in Total Quality Assurance, offering a comprehensive suite of services to support the medical device industry. For medical device EMC testing, Intertek provides specialized expertise to ensure your products comply with stringent electromagnetic compatibility regulations. Their testing services help manufacturers navigate complex international standards, reducing time-to-market and mitigating risks associated with non-compliance. By partnering with Intertek, you gain access to state-of-the-art testing facilities and a team of experienced professionals dedicated to verifying the safety and performance of your medical devices in diverse electromagnetic environments. Their commitment extends to ensuring that medical devices not only meet but exceed industry expectations for reliability and safety. Intertek's rigorous testing protocols are designed to identify and address potential electromagnetic interference issues, safeguarding both patient well-being and device functionality. This focus on quality and compliance makes Intertek a trusted partner for medical device manufacturers seeking to achieve global market access and maintain a competitive edge.

Website: intertek.com

HQ: GB

Countries: United States, United Kingdom, China, Canada, Japan, India, Brazil, Europe, Asia

Languages: English

Standards: IEC 60601-1-2

Test Coverage: EMC only

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TÜV SÜD

TÜV SÜD is a leading global testing, inspection, and certification company. They offer comprehensive EMC testing services for medical devices.

TÜV SÜD is a globally recognized leader in testing, inspection, and certification services, dedicated to enhancing safety, security, and sustainability. For the medical device industry, they provide specialized EMC (Electromagnetic Compatibility) testing to ensure devices meet stringent regulatory requirements and function reliably in their intended environments. Their expertise covers a wide range of medical devices, helping manufacturers navigate complex international standards and achieve market access. By partnering with TÜV SÜD, companies can gain confidence in their product's compliance and performance, ultimately protecting patient safety and brand reputation. Leveraging extensive experience and state-of-the-art facilities, TÜV SÜD's EMC testing services are crucial for medical device manufacturers seeking to validate the electromagnetic performance of their products. This includes assessing susceptibility to electromagnetic disturbances and ensuring that emissions do not interfere with other devices.

Website: tuvsud.com

HQ: Germany

Languages: English

Pricing model: Per project

Lead Time: Start in 2-4 weeks

Quote SLA: 3-5 business days

Rush Available: Yes

Standards: IEC 60601-1, IEC 60601-1-2, IEC 60601-1-11

Test Coverage: Both

Accredited: Yes

Max EUT Size: Large

Pre-Scan/Debug: Yes

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TÜV Rheinland

TÜV Rheinland is a global leader in testing, inspection, and certification services, specializing in medical device EMC testing and compliance for global market access.

TÜV Rheinland is a world-leading provider of technical services with 150 years of experience in ensuring safety and quality. They offer comprehensive testing, inspection, and certification solutions for medical devices, including expertise in IEC 60601-1 standards and electromagnetic compatibility (EMC). Their services are crucial for manufacturers seeking to navigate complex regulatory landscapes and achieve global market access for their products. TÜV Rheinland's highly qualified experts provide independent quality assurance, enabling innovation and assisting companies in meeting international standards and compliance requirements. With a strong focus on sustainability and emerging technologies, TÜV Rheinland partners with businesses to ensure their products are safe, reliable, and compliant, contributing to a safer and better future.

Website: tuv.com

HQ: DE

Languages: English

Standards: IEC 60601-1

Test Coverage: Both

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SGS

SGS&CO offers brand consulting, AI solutions, automation, analytics, and insights for modern brands. They leverage technology to meet creative production needs.

SGS&CO is a provider specializing in brand consulting, AI solutions, automation, analytics, and insights. They are dedicated to empowering modern brands within the creative production ecosystem by harnessing the power of artificial intelligence, data management, automation, and analysis. Their services are tailored to meet the evolving needs of brands, offering advanced technological solutions to enhance creative production processes. SGS&CO focuses on building new futures at scale, working with partners to deliver impactful results through data-driven strategies and innovative technologies.

Website: sgsco.com

HQ: East Syracuse, US

Countries: United States, Canada

Languages: English

Standards: IEC 60601-1-2

Test Coverage: EMC only

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CSA Group

CSA Group offers comprehensive program and construction management, design, architecture, environmental, and engineering services. They specialize in project delivery and program management for various markets.

CSA Group is a full-service project delivery and program management company. They merge comprehensive architectural, engineering, and environmental capabilities with project, technical, and construction expertise to define, plan, integrate, and implement every aspect of a client's portfolio of projects. Their services span Program Management, Construction Management, Design and Architecture, to Environmental and Engineering, all delivered with a focus on results. They address interrelated issues such as architecture, engineering design, and environmental compliance, providing comprehensive solutions. CSA Group also coordinates response and recovery efforts, evaluates vulnerable assets and critical infrastructure, and supports recovery of eligible costs. Their offices are located across the US Northeast Corridor, US Southeast Corridor, the Caribbean, and Latin America, serving both national and international clients. CSA Group is actively involved in industry advancements, as evidenced by their participation in initiatives like the Disaster Recovery Coalition of America (DRCA) and workshops for early warning systems. They also showcase their project successes and leadership at industry events.

Website: csagroup.com

HQ: New York City, US

Countries: United States

Languages: English

Standards: IEC 60601-1, IEC 60601-1-2, IEC 61010-1

Test Coverage: Both

Max EUT Size: Custom

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Nemko

Nemko offers global market access, product testing, and certification services for electrical products. Established in 1933, they provide comprehensive solutions to ensure compliance and reduce time to market.

Since 1933, Nemko has been a trusted partner in ensuring product compliance worldwide. They specialize in global market access, product testing, and certification for electrical products, offering a one-stop-shop solution to streamline processes and accelerate time to market. Their services encompass pre-compliance, product certification, cyber assurance, field evaluation, management system certification, and functional safety, among others. With over 90 years of experience, Nemko is dedicated to safety, security, and sustainability, helping clients navigate complex regulatory landscapes and stay ahead of innovation. They are committed to delivering a great customer experience, promoting continuous learning, and caring for people and the environment.

Website: nemko.com

HQ: Norway

Countries: United States, United Kingdom, China, Canada, Italy, Japan, South Korea, Brazil, Norway, Poland, Europe, Asia

Languages: English

Pricing model: Custom pricing

Lead Time: Start in 4-8 weeks

Quote SLA: 3-5 business days

Standards: IEC 60601-1-2

Test Coverage: EMC only

Accredited: Yes

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DEKRA

DEKRA offers comprehensive EMC testing services for medical devices, ensuring compliance with global standards. Leverage their expertise for safe and reliable product certification.

DEKRA is a leading global testing, inspection, and certification company. For the medical device industry, DEKRA provides specialized EMC (Electromagnetic Compatibility) testing to ensure that devices operate safely and effectively without causing or being affected by electromagnetic interference. This is crucial for regulatory approval and market access in regions like the EU and the US. Their services help manufacturers navigate complex compliance requirements, including CE marking and FDA submissions. By partnering with DEKRA, companies can accelerate their product development cycles and gain confidence in their device's performance and safety. DEKRA's accredited laboratories and expert teams are dedicated to supporting innovation and ensuring that medical devices meet the highest standards of quality and reliability.

Website: dekra.com

HQ: DE

Countries: Global

Languages: English

Pricing model: Custom pricing

Lead Time: Start in 4-8 weeks

Quote SLA: 3-5 business days

Rush Available: Yes

Standards: IEC 60601-1-2

Test Coverage: EMC only

Accredited: Yes

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Element Materials Technology

Element U.S. Space & Defense, formerly NTS Technical Systems, offers specialized EMC/EMI testing and engineering services for the medical device industry. They are a trusted partner for mission-critical programs, providing advanced testing to ensure product compliance and readiness.

Element U.S. Space & Defense, a division of Element Materials Technology, is a premier provider of testing and engineering services, with a strong focus on EMC/EMI testing relevant to the medical device industry. Formerly known as NTS Technical Systems, the company has a rich history dating back to 1961, evolving to become a trusted partner for mission-critical programs. Leveraging state-of-the-art facilities and deep subject matter expertise, Element U.S. Space & Defense offers a comprehensive suite of services designed to ensure products meet rigorous compliance standards. Their capabilities include advanced EMI/EMC testing, environmental simulations, dynamics, hydraulics, and ordnance testing, among others. This broad range of services allows them to support clients in accelerating product development and market entry. With strategically located laboratories, including facilities in Belcamp, MD, and Camden, AR, Element U.S. Space & Defense is equipped to handle complex testing requirements. They are accredited by numerous international standards bodies, including ISO/IEC 17025, and hold specific approvals for various industry-specific testing protocols. Their commitment to technical excellence and meeting stringent scheduling requirements makes them an ideal partner for organizations seeking reliable and advanced testing solutions.

Website: elementdefense.com

HQ: Belcamp, US

Countries: United States, United Kingdom, Europe, Asia

Languages: English

Pricing model: Custom pricing

Lead Time: Start in 4-8 weeks

Quote SLA: 3-5 business days

Standards: ISO/IEC 17025

Test Coverage: Both

Accredited: Yes

Max EUT Size: Custom

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Bureau Veritas

Bureau Veritas is a global leader in testing, inspection, and certification services, ensuring quality, safety, and sustainability for businesses worldwide. They specialize in helping clients navigate complex regulations and achieve their performance goals.

Bureau Veritas is a world leader in laboratory testing, inspection, and certification services. They offer a comprehensive suite of services designed to enhance performance, mitigate risk, and promote sustainable business practices across various industries. With a global network of state-of-the-art laboratories and field expertise, Bureau Veritas supports clients in ensuring their products, systems, and services comply with applicable standards, regulations, and specifications. Their core mission is to foster trust and ensure responsible progress by helping clients manage quality, safety, health, and sustainability risks. Bureau Veritas's strategy, LEAP | 28, focuses on portfolio enhancement, performance improvement, and people development, with sustainability at its core. They are committed to being a preferred partner for their customers' excellence and sustainability journeys, addressing critical challenges and aligning with societal aspirations. For the medical device EMC testing directory, Bureau Veritas provides crucial expertise in ensuring that medical devices meet stringent electromagnetic compatibility (EMC) standards. This involves rigorous testing and certification to guarantee the safety and reliability of devices in complex electromagnetic environments, thereby facilitating market access and maintaining compliance.

Website: group.bureauveritas.com

HQ: France

Countries: United States, India, Mexico, Asia

Languages: English

Pricing model: Custom pricing

Lead Time: Start in 4-8 weeks

Quote SLA: 3-5 business days

Rush Available: Yes

Standards: IEC 60601-1, IEC 60601-1-2, IEC 60601-1-11

Test Coverage: Both

Accredited: Yes

Max EUT Size: Large

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Acertara Acoustic Laboratories LLC

Acertara Acoustic Laboratories offers specialized services for diagnostic ultrasound probes, including repair, testing, calibration, and FDA 510(k) submission consulting. They ensure probe safety and performance for healthcare providers.

Acertara Acoustic Laboratories LLC is a leading provider of specialized services for diagnostic ultrasound probes, dedicated to enhancing probe performance, safety, and extending their lifecycle. They offer comprehensive solutions including expert probe repair, validated ultrasound probe testing under ISO/IEC 17025:2017 standards, and precise acoustic measurement & calibration services. With extensive experience and ISO13485:2016 certification, Acertara assists clients in navigating the complexities of FDA 510(k) submissions and regulatory consulting, streamlining the device clearance process. Their world-class R&D team utilizes patented testing devices and adheres to rigorous scientific and regulatory standards to ensure the highest quality outcomes for healthcare providers, research laboratories, and medical device manufacturers. Acertara's commitment to innovation, integrity, and accuracy makes them a trusted partner for maintaining the reliability and safety of critical medical equipment, ultimately contributing to better patient care and sustainable cost management within the healthcare industry.

Website: acertaralabs.com

HQ: Longmont, US

Countries: United States, Europe

Languages: English

Standards: ISO/IEC 17025

Test Coverage: Safety only

Accredited: Yes

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Medical Equipment Compliance Associates, Inc.

MECA provides expert medical and laboratory equipment compliance testing and documentation for global regulatory bodies. They are leaders in medical device safety, serving top manufacturers worldwide.

Medical Equipment Compliance Associates, Inc. (MECA) specializes in providing high-quality testing and documentation to ensure compliance with medical and laboratory equipment standards, primarily IEC 60601-1 and IEC 61010-1. Their services are crucial for submitting documentation to global regulatory bodies. MECA actively participates in the Standards Development Process as technical experts on various IEC and AAMI committees, ensuring they are at the forefront of compliance knowledge. MECA aims to streamline the often difficult and time-consuming process of obtaining evidence of compliance. They leverage their expertise to minimize surprises and resolve issues efficiently. The company boasts a strong track record, servicing 8 of the Top 10 Medical Manufacturers Worldwide since 2002. Their engineers are directly involved in global standards development and application processes, including IEC, ISO, AAMI, and IECEE. Services offered include Preliminary Evaluation, Preliminary Testing, Medical Device or Laboratory Equipment Evaluation, Electromagnetic Compatibility (EMC) Evaluation, Wireless Global Access, and FDA ASCA Program support. They also offer Compliance Services as a retainer for expert consultation, and Seminars to equip teams with knowledge of appropriate standards. MECA helps clients reduce costs and time by identifying potential compliance issues early in the design process.

Website: 60601-1.com

HQ: Oak Creek, US

Countries: United States

Languages: English

Pricing model: Custom pricing

Standards: IEC 60601-1, IEC 60601-1-2, IEC 61010-1

Test Coverage: Both

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Retlif Testing Laboratories, Inc.

Retlif Testing Laboratories offers comprehensive EMC/EMI and ESS/Environmental testing services, including engineering support and training, for medical device compliance. They are accredited to ISO/IEC 17025 and recognized by NAVAIR.

Retlif Testing Laboratories, Inc. is a leading provider of comprehensive Electromagnetic Compatibility (EMC) and Environmental Simulation Solutions (ESS) testing services, with a strong focus on supporting the medical device industry's compliance needs. With three state-of-the-art testing facilities located in Ronkonkoma, New York; Goffstown, New Hampshire; and Harleysville, Pennsylvania, Retlif offers a full spectrum of testing and compliance engineering services. They are accredited to ISO/IEC 17025 with over 140 accredited test methods and are recognized by NAVAIR for military EMC testing. Retlif tests to domestic US and international standards, including those required for medical devices, aerospace, rail, maritime, commercial, and industrial applications. Beyond core testing, Retlif provides specialized engineering support, including the development of test-specific documentation and pre-design compliance consulting to help clients navigate complex regulatory requirements. They also offer customized training programs to educate organizations and professionals on EMC/EMI and ESS principles. Retlif's commitment to quality and customer satisfaction ensures globally accepted test results, facilitating product acceptance across various markets.

Website: retlif.com

HQ: Ronkonkoma, USA

Countries: United States, United Kingdom, Canada, Japan, Australia, Europe

Languages: English

Standards: ISO/IEC 17025

Test Coverage: Both

Accredited: Yes

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DLS Electronic Systems, Inc.

D.L.S. Electronic Systems, Inc. is a full-service laboratory offering testing, consulting, and engineering services for EMI/EMC, Wireless, Product Safety, Environmental, and Cybersecurity needs. They are an ANAB accredited test facility.

D.L.S. Electronic Systems, Inc. is a comprehensive testing and consulting firm specializing in EMI/EMC, Wireless, Product Safety, Environmental, and Cybersecurity compliance. As an ANAB accredited test facility, they offer extensive services including testing, consulting, and engineering to ensure products meet regulatory requirements across various industries. Their expertise extends to designing products for compliance and resolving complex issues. With multiple test chambers and open area test sites, D.L.S. can perform a wide range of tests up to 40 GHz. They are equipped to handle environmental testing, including climatic and mechanical tests, as well as product safety testing for global markets (US, Canada, Europe, UK, Australia). Their services cater to industries such as Medical Equipment, Automotive, Aerospace, Computer, Industrial Equipment, Military, and Telecommunications. Specifically for the medical device industry, D.L.S. provides testing and consulting for standards like EN IEC 60601-1-11, which addresses basic safety and essential performance for medical electrical equipment in home healthcare environments. They understand the unique requirements of this sector, including more stringent temperature and humidity controls, and handling/storage considerations.

Website: dlsemc.com

HQ: Wheeling, US

Languages: English

Standards: IEC 60601-1-11, ISO/IEC 17025

Test Coverage: Both

Accredited: Yes

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Sigma Scientific Services LLC

If you require our professional assistance for the FDA and FDA registration and listing services, then do not worry and feel free to contact Sigma Biomedical.

Website: sigmabiomedical.com

HQ: Canada

Countries: Canada, Japan, Europe

Languages: English

Pricing model: Custom pricing

Lead Time: Start in 4-8 weeks

Quote SLA: 3-5 business days

Standards: IEC 60601-1-2

Test Coverage: EMC only

Accredited: No

Max EUT Size: Custom

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Washington Laboratories, Ltd.

Schweitzer Engineering Laboratories (SEL) provides advanced solutions for power systems, including engineering, manufacturing, and technical support. They focus on improving power system reliability and efficiency.

Schweitzer Engineering Laboratories (SEL) is a global leader in providing advanced solutions for power systems. Since 1984, SEL has grown to over 7,000 employees worldwide, dedicated to improving power system reliability and efficiency. Their core values of quality, integrity, and community drive everything they do, with a unique employee ownership strategy ensuring long-term customer focus and stability. SEL offers a comprehensive range of services and products designed to meet the evolving needs of the electric power industry. They partner with customers globally to enhance power system performance through innovative engineering, manufacturing, and technical support. The company's commitment to innovation is also highlighted by initiatives like the Schweitzer Drive podcast, exploring the future of electric power. With a strong emphasis on customer support and long-term relationships, SEL ensures that their solutions are not only technologically advanced but also sustainable and reliable. Their dedication to excellence makes them a trusted partner for organizations seeking to optimize their power infrastructure.

Website: wll.com

HQ: Pullman, US

Languages: English

Pricing model: Custom pricing

Lead Time: Start in 4-8 weeks

Quote SLA: 3-5 business days

Rush Available: Yes

Standards: IEC 60601-1, IEC 60601-1-2, IEC 60601-1-11

Test Coverage: Both

Accredited: Yes

Max EUT Size: Large

Pre-Scan/Debug: Yes

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VPI Laboratories, Inc.

VPI Laboratories, Inc. (Virginia Physicians, Inc.) is a healthcare provider serving Central Virginia since 1923. They offer a wide range of medical services and have multiple locations across the region.

VPI Laboratories, Inc., operating as Virginia Physicians, Inc., has been a cornerstone of healthcare in Central Virginia since 1923. Their mission is to deliver compassionate, high-quality medical services through the collaborative efforts of their physicians and staff. The organization emphasizes a patient-centered approach, offering access to a patient portal for managing medical records, scheduling appointments, and accessing lab reports. With a commitment to accessible care, VPI Laboratories, Inc. provides services across various locations in Chesterfield, Hanover, Henrico, and Powhatan. They offer a diverse range of medical specialties and advanced practice clinicians. Patients can benefit from services like telemedicine appointments, customized diets, and nutritional counseling, reflecting their dedication to comprehensive patient well-being. The organization also prioritizes clear communication and patient information, as evidenced by their privacy policy detailing the use and disclosure of protected health information. VPI Laboratories, Inc. continues to evolve its services to meet the healthcare needs of the Central Virginia community.

Website: vpitechnology.com

HQ: Richmond, US

Languages: English

Pricing model: Custom pricing

Lead Time: Start in 4-8 weeks

Quote SLA: 3-5 business days

Rush Available: Yes

Standards: IEC 60601-1-2

Test Coverage: EMC only

Accredited: No

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MedTech Testing Solution Co., Ltd.

Intelligent Bio Solutions (INBS) offers rapid, non-invasive drug testing solutions using fingerprint sweat analysis. Their innovative products, including the SmarTest Patch, cater to various industries and are expanding into the US market.

Intelligent Bio Solutions Inc. (INBS) is a medical technology company specializing in intelligent, rapid, and non-invasive testing solutions. Their core offering, the Intelligent Fingerprinting Drug Testing Solution, detects commonly abused drugs via sweat from fingertips, providing results within minutes for recent drug use. This system is designed for ease of use and portability, making it suitable for reliable drug screening and identification of potential misuse within the 16-24 hours prior to testing. Expanding their product line, the SmarTest Patch is a discreet, wearable device for longer-term monitoring, detecting drug use through sweat over a 7 to 10-day period. This offers a complete non-invasive, sweat-based solution for both immediate and continuous drug detection when used alongside their screening system. With a recent FDA 510(k) submission and planned US market entry in 2025, INBS is poised to capitalize on the growing drug screening market. Strategic partnerships enhance their global manufacturing capacity and supply-chain resilience, accelerating the adoption of their intelligent testing technologies.

Website: medtechtesting.com.tw

HQ: New York, US

Languages: English

Pricing model: Custom pricing

Lead Time: Start in 4-8 weeks

Quote SLA: 3-5 business days

Standards: IEC 60601-1-2

Test Coverage: EMC only

Accredited: No

Max EUT Size: Custom

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MEQUIPE S.r.l.

MEQUIPE S.r.l. Unipersonale is a specialized laboratory offering integrated product and system certification services for the medical device industry, including EMC testing and CE marking.

MEQUIPE S.r.l. Unipersonale is a leading laboratory with extensive expertise in the electrical and electronic medical device sector. They provide comprehensive 360° services required by manufacturers, including electrical, mechanical, and environmental safety testing crucial for CE marking. With a decade of experience in R&D and a deep understanding of regulations and directives, MEQUIPE offers specialized knowledge to companies in the electrical, electronic, and particularly the medical fields. Their mission is to professionally address any challenge in product and system certification, emphasizing competence, experience, and ethical conduct. Services include complete and partial testing, end-of-production-line testing, design validation testing, and special testing according to technical specifications, alongside technical file preparation, risk analysis, and quality management systems.

Website: mequipe.it

HQ: San Donato Milanese, IT

Countries: Italy, Europe, Asia

Languages: English

Pricing model: Custom pricing

Standards: IEC 60601-1, IEC 60601-1-2

Test Coverage: Both

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ELETTRA s.r.l.

CEMAS Elettra is a global leader in plastic welding technologies, offering innovative and reliable solutions for various industries. With 40+ years of experience, they provide end-to-end project support, from consulting and design to manufacturing and after-sales assistance.

CEMAS Elettra is a global leader in plastic welding technologies, delivering innovative, reliable, and tailor-made solutions for industries worldwide. With over 40 years of experience, they offer comprehensive end-to-end project support, encompassing initial consulting, technical feasibility, design, prototyping, welding trials, and after-sales assistance. Their expertise ensures a smooth, efficient, and high-performance production process, helping clients reduce risks, save time, and stay competitive. The company's in-house design department specializes in creating customized welding machines and equipment using advanced CAD software. They also provide rapid prototyping services to validate designs before full-scale production. CEMAS Elettra's Process Development Center conducts extensive welding trials to fine-tune parameters and guarantee optimal performance, with pilot production runs to ensure a smooth transition to manufacturing. With a strong global presence, CEMAS Elettra ensures proximity and responsiveness through its network of branches. Their commitment extends to ongoing technical support and maintenance services, aiming to build long-term partnerships and empower clients' teams. They are certified ISO 9001 and ISO 14001, reflecting their dedication to quality, sustainability, and excellence.

Website: elettra.it

HQ: Carmagnola, Italy

Languages: English

Standards: ISO/IEC 17025

Test Coverage: EMC only

Accredited: Yes

Max EUT Size: Custom

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Hermon Laboratories, Ltd.

Hermon Laboratories is Israel's leading compliance testing and certification company for electronic and electrical products, specializing in EMC, Product Safety, Radio, Telecom, and Environmental testing since 1987.

Hermon Laboratories, Ltd. is Israel's largest and leading company for compliance testing and certification of electronic and electrical products, serving the hi-tech industry since 1987. They offer a one-stop-shop solution for EMC, Product Safety, Radio, Telecom, and Environmental testing, catering to a broad range of commercial, industrial, military, and medical products. With a comprehensive portfolio of accreditations from local and global regulatory bodies, Hermon Laboratories provides turnkey certification solutions worldwide. Their state-of-the-art testing facilities are located in Binyamina and Tel Aviv. The experienced team of compliance engineers guides clients from initial product specification and design through to meeting mandatory standards for product marketing, ensuring products reach the market quickly and efficiently. They are experts in global compliance solutions, including specific services for Medical Devices and Radio Frequency Communication Services (RF) testing, ensuring adherence to international laws like FCC and RED.

Website: hermonlabs.com

HQ: Binyamina, Israel

Countries: United States, Canada, Japan, Australia, Europe

Languages: English

Pricing model: Custom pricing

Lead Time: Start in 0-2 weeks

Quote SLA: < 24 hours

Standards: IEC 60601-1-2

Test Coverage: Both

Accredited: Yes

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The Standards Institution of Israel

ISO develops and publishes international standards to ensure products and services are safe, reliable, and of high quality. They facilitate global trade and cooperation.

The International Organization for Standardization (ISO) is a global network of national standards bodies dedicated to developing and publishing international standards. These standards ensure that products and services are safe, reliable, and of high quality, making lives easier, safer, and better for everyone. ISO standards cover a vast range of sectors, including Health, IT & related technologies, Management & services, and Environmental sustainability. ISO is an independent, non-governmental international organization that brings together global experts to agree on the best ways of doing things. While ISO does not provide certification or conformity assessment services directly, its standards are crucial for businesses seeking to demonstrate quality and compliance. Membership is open only to national standards institutes, with one member per country representing ISO locally. Through its consensus-based development process, ISO ensures that standards address clear market requirements and the needs of various industries and stakeholders. By facilitating trade and cooperation, ISO plays a vital role in solving global challenges and promoting best practices worldwide.

Website: managementsystems.world

HQ: Vernier, CH

Countries: United States, United Kingdom, Germany, Europe, Asia

Languages: English

Pricing model: Per project

Lead Time: Start in 4-8 weeks

Quote SLA: 3-5 business days

Standards: IEC 60601-1-2

Test Coverage: EMC only

Max EUT Size: Large

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CCIC-CSA International Certification Co., Ltd.

CCIC-CSA International Certification Co., Ltd. offers accreditation services for various industries, including medical device EMC testing. They ensure compliance with international standards.

CCIC-CSA International Certification Co., Ltd., operating as the International Accreditation Service (IAS), provides comprehensive accreditation programs designed to ensure worldwide acceptance and build trust. They base their programs on internationally recognized standards, developing accreditation criteria through public hearings to offer clear guidelines for performance features. IAS offers specialized accreditation for sectors such as Aerospace Quality Management System Certification Bodies, Building Departments and Third-Party Service Providers, and Calibration Laboratories. For calibration laboratories, IAS accreditation is recognized through MRAs with APAC and ILAC, promoting international trade by fostering confidence in accredited calibration certificates and test reports. The organization emphasizes the benefits of accreditation, highlighting how it supports international trade and ensures compliance with the latest versions of standards like ISO/IEC 17021 and ISO 9001. IAS also provides resources such as webinars and informational lists to assist organizations in understanding and achieving accreditation.

Website: csagroup.org

HQ: Metairie, US

Languages: English

Pricing model: Custom pricing

Quote SLA: < 24 hours

Standards: ISO/IEC 17025

Test Coverage: EMC only

Accredited: Yes

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Centre Testing International Group Co., Ltd.

Social Accountability International (SAI) is a global leader in promoting social responsibility and improving working conditions worldwide. They offer expertise in social compliance, human rights, and sustainable business practices.

Social Accountability International (SAI) is dedicated to improving working conditions, advancing human rights, and advocating for better social performance across organizations globally. With over 20 years of experience, SAI provides a comprehensive suite of services designed to help companies measure, manage, and improve their social impact. SAI's offerings include corporate programs focused on developing a culture of continual improvement and embedding sustainable solutions within businesses and their supply chains. Their Social Fingerprint® tool allows companies to measure and improve social performance, identifying root causes of workplace issues and fostering a management-systems approach. Furthermore, SAI, through its division Social Accountability Accreditation Services (SAAS), provides independent accreditation for social auditing systems, ensuring quality, consistency, and transparency in social certification programs. Through initiatives like TenSquared, a 100-day accelerated change program, SAI empowers workers and managers to collaboratively solve workplace challenges. They also maintain a Consultant Registry to promote professionalism and transparency in social accountability consulting. SAI's work is grounded in international human rights standards and ILO Conventions, aiming to create decent workplaces and advance human rights globally.

Website: cti-cert.com

HQ: New York, United States of America

Languages: English

Pricing model: Per project

Lead Time: Start in 4-8 weeks

Quote SLA: 3-5 business days

Standards: IEC 60601-1

Test Coverage: Both

Accredited: No

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Intertek Testing Services Shenzhen Ltd.

Intertek Testing Services Shenzhen Ltd. offers expert EMC testing for medical devices, ensuring compliance and market access. Located in Shenzhen, China, they provide reliable testing solutions.

Intertek Testing Services Shenzhen Ltd. is a leading provider of comprehensive EMC (Electromagnetic Compatibility) testing services specifically tailored for the medical device industry. Situated in Shenzhen, China, a hub for technological innovation, Intertek leverages its extensive expertise and state-of-the-art facilities to ensure that medical devices meet stringent international EMC standards. Their services are crucial for manufacturers seeking to obtain regulatory approvals and successfully launch their medical devices into global markets. By identifying and mitigating potential electromagnetic interference issues early in the product development cycle, Intertek helps clients avoid costly redesigns and delays. The company's commitment to quality and accuracy makes them a trusted partner for medical device companies worldwide. Intertek Testing Services Shenzhen Ltd. is dedicated to providing efficient and reliable testing solutions. Their team of experienced engineers works closely with clients to understand their specific product requirements and testing needs, offering customized approaches to achieve compliance. This focus on client collaboration and technical proficiency ensures that medical devices are not only compliant but also perform optimally in their intended environments.

Website: intertek.com

HQ: Shenzhen, China

Countries: United States, United Kingdom, China, Canada, Japan, India, Brazil, Europe, Asia

Languages: English

Pricing model: Per project

Lead Time: Start in 2-4 weeks

Quote SLA: 24-48 hours

Rush Available: Yes

Standards: IEC 60601-1, IEC 60601-1-2

Test Coverage: EMC only

Accredited: Yes

Pre-Scan/Debug: Yes

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Intertek Testing Services, NA, Inc.

Intertek Testing Services, NA, Inc. offers specialized medical device EMC testing. They are a leading provider of quality and regulatory solutions.

Intertek Testing Services, NA, Inc. is a premier provider of comprehensive testing services, with a specific focus on Electromagnetic Compatibility (EMC) for medical devices. Their expertise ensures that medical equipment meets stringent regulatory standards, safeguarding patient safety and device efficacy. Leveraging extensive industry knowledge and state-of-the-art facilities, Intertek assists manufacturers in navigating the complex landscape of medical device compliance. They are dedicated to delivering reliable and efficient testing solutions, helping clients bring their innovative products to market with confidence. As a trusted partner, Intertek Testing Services, NA, Inc. is committed to upholding the highest levels of quality and integrity in all their operations, making them an invaluable resource for the medical device industry.

Website: intertek.com

HQ: US

Languages: English

Pricing model: Per project

Lead Time: Start in 2-4 weeks

Quote SLA: 24-48 hours

Rush Available: Yes

Standards: IEC 60601-1, IEC 60601-1-2, IEC 60601-1-11

Test Coverage: EMC only

Accredited: Yes

Pre-Scan/Debug: Yes

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Eurofins Electrical and Electronic Testing NA, Inc.

Eurofins offers comprehensive medical device testing services, including sterile barrier integrity, shelf life, and packaging evaluations. They ensure safety, efficacy, and quality compliance for market launch and post-marketing activities.

Eurofins provides a global network of experts and laboratories dedicated to the development and lifecycle management of medical devices. Their services encompass consulting, testing, and sterile packaging, ensuring products meet regulatory requirements and industry trends for rapid market entry. Specializing in critical areas like Sterile Barrier Integrity Testing (per ISO 11607, ASTM F1929, ASTM F2096) and Shelf Life & Accelerated Aging studies, Eurofins utilizes state-of-the-art labs with extensive storage and environmental chambers. Their Package Testing Lab is GMP, ISTA certified, and ISO 17025 accredited, evaluating all aspects of packaging configurations to withstand global transit. With over 40 years of expertise, Eurofins assists companies of all sizes in achieving safety, efficacy, and quality compliance for their medical devices, from raw materials to finished goods. They offer comprehensive solutions to manage the entire lifecycle of medical devices.

Website: metlabs.com

HQ: Baltimore, United States

Countries: United States, Canada, Japan, South Korea, Australia, Europe, Asia

Languages: English

Pricing model: Custom pricing

Standards: ISO/IEC 17025

Test Coverage: Both

Accredited: Yes

Max EUT Size: Custom

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Eurofins Electrical Testing Service (Shanghai) Co., Ltd.

Eurofins Electrical Testing Service (Shanghai) Co., Ltd. offers specialized EMC testing for medical devices. Leverage their global network and expertise for product compliance and market readiness.

Eurofins Electrical Testing Service (Shanghai) Co., Ltd. is a key part of Eurofins Scientific's global network, providing essential EMC testing services for the medical device industry. They assist companies throughout the product lifecycle, from development to post-marketing, ensuring compliance with stringent regulatory requirements. With a focus on safety, efficacy, and quality, their state-of-the-art laboratories and experienced regulatory experts help clients navigate complex standards like ISO 11607 and ASTM F1929. Eurofins offers comprehensive solutions including sterile barrier integrity testing, shelf life and accelerated aging studies, and packaging evaluations, all designed to facilitate market access and maintain product integrity throughout distribution and storage. Their commitment to precision, proficiency, and proximity makes them a trusted partner for medical device manufacturers worldwide.

Website: enec.com

HQ: Shanghai, China

Languages: English

Pricing model: Custom pricing

Standards: ISO/IEC 17025

Test Coverage: Both

Accredited: Yes

Max EUT Size: Custom

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Bay Area Compliance Laboratories

Bay Area Compliance Laboratories (BACL) is a worldwide certification body and testing laboratory providing regulatory testing and certification for a wide range of products, including medical devices.

Bay Area Compliance Laboratories Corp. (BACL) is a globally recognized testing laboratory and certification body specializing in regulatory compliance for a diverse array of products. They offer comprehensive solutions for testing and certification, ensuring products meet international market access requirements. BACL leverages extensive expertise to deliver timely and dependable results, facilitating a faster and more cost-effective product development to market transition. Accredited to ISO/IEC 17025:2017 by A2LA, BACL's scope includes Electromagnetic Compatibility (EMC), Product Safety, Licensed Radio and Unlicensed Wireless Devices, Wireline Telecommunications, and Lighting. They are also a US EPA ENERGY STAR Recognized Test Laboratory and an approved test laboratory by the California Energy Commission. Their services are crucial for companies seeking to validate product quality and compliance for global distribution. BACL stays current with evolving international regulations, as evidenced by their updates on requirements in Chile (SUBTEL), Mexico (IFT), and Jordan (TRC). This proactive approach ensures clients are informed about the latest compliance mandates, such as QR code requirements for wireless devices in Chile and new technical regulations for wireless LAN equipment in Mexico.

Website: baclcorp.com

HQ: Milpitas, US

Languages: English

Rush Available: Yes

Standards: ISO/IEC 17025

Test Coverage: Both

Accredited: Yes

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MET Laboratories, Inc.

MET Laboratories, Inc. is a leading provider of testing and certification services for medical devices, specializing in EMC, wireless, and product safety. They are an FDA ASCA-Accredited Laboratory.

MET Laboratories, Inc., now part of Eurofins Scientific, is a globally recognized leader in product testing and regulatory certification, established in 1959. They offer comprehensive services for the medical device industry, including Electromagnetic Compatibility (EMC) testing, wireless and RF testing, and product safety testing. MET is an FDA ASCA-Accredited Laboratory for Premarket Testing of Medical Devices, ensuring compliance with stringent industry standards. With extensive expertise, MET helps manufacturers navigate complex regulatory landscapes, ensuring their products are safe, compliant, and ready for global market access. Their services encompass testing for wireless coexistence, ensuring devices operate reliably in proximity to other wireless technologies. They are also an OSHA-recognized NRTL, with their MET Mark accepted by federal and local authorities, retailers, and consumers. MET Laboratories provides end-to-end solutions, from initial development through final certification. Their state-of-the-art facilities and experienced team ensure efficient and cost-effective testing, accelerating time-to-market for critical medical devices. They are committed to exceeding expectations and providing partners with the assurance needed for global market success.

Website: metlabs.com

HQ: Baltimore, MD, US

Languages: English

Lead Time: Start in 2-4 weeks

Quote SLA: < 24 hours

Rush Available: Yes

Standards: ISO/IEC 17025

Test Coverage: Both

Accredited: Yes

Pre-Scan/Debug: Yes

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Compliance Testing, LLC

Accredited lab offering FCC, CE, and medical device EMC testing. Specializing in compliance for global market access since 1963.

Compliance Testing, LLC is an ANAB-accredited testing laboratory with over 60 years of experience providing comprehensive EMC and EMI testing services. We specialize in helping manufacturers achieve crucial certifications for electronic devices, including FCC, CE, and IEC 60601-1-2 for medical devices, ensuring your products meet regulatory requirements for global market access. Our expert team guides clients through the complex certification process, offering personalized service and leveraging state-of-the-art equipment. We cater to a wide range of industries and markets, including the US, Canada, European Union, Australia, New Zealand, Korea, and Japan. Compliance Testing is committed to making the certification process fast, simple, and stress-free, helping you bring your products to market quickly and grow your revenue.

Website: compliancetesting.com

HQ: US

Countries: United States, China, Canada, Japan, South Korea, Australia, Singapore, Europe

Languages: English

Quote SLA: < 24 hours

Standards: IEC 60601-1-2

Test Coverage: Both

Accredited: Yes

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TIMCO Engineering, Inc.

TIMCO Engineering, Inc. offers comprehensive EMC and telecommunications testing services for medical devices and other electronic products. With nearly 50 years of experience, they provide product certification to help bring innovative products to market.

TIMCO Engineering, Inc. is a leading provider of Electromagnetic Compatibility (EMC) and telecommunications testing services, specializing in helping bring innovative electronic products to market. With nearly 50 years of expertise, they offer comprehensive product certification for a wide range of devices, including medical devices, marine radars, and radio frequency devices. Their services are crucial for ensuring that products meet regulatory requirements and perform reliably in their intended environments. TIMCO Engineering, Inc. is accredited by various agencies, including ISO 17025:2017, ISO 17065:2012, and NADCAP, demonstrating their commitment to quality and accuracy. They operate multiple labs across the United States and Canada, with a headquarters in Alpharetta, GA, ensuring broad coverage and accessibility for their clients. TIMCO Engineering, Inc. is dedicated to providing professional, fast, and accurate service, focusing on understanding client challenges and delivering successful solutions. Their commitment to safety, efficiency, and compliance makes them a trusted partner for manufacturers seeking to certify their electronic products.

Website: industrial-ia.com

HQ: Alpharetta, US

Languages: English

Quote SLA: 24-48 hours

Standards: ISO/IEC 17025

Test Coverage: Both

Accredited: Yes

Max EUT Size: Custom

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Elite Electronic Engineering, Inc.

Elite Electronic Engineering, Inc. offers comprehensive EMC/EMI, environmental stress, and photometric testing services. Founded in 1954, they are a leader in product qualification and compliance testing for automotive, aerospace, military, and telecommunications industries.

Founded in 1954, Elite Electronic Engineering, Inc. is a full-service electromagnetic compatibility/interference (EMC/EMI), environmental stress, and photometric testing laboratory. They are a premier test provider for the automotive, aerospace, military, heavy equipment, electronics, and telecommunications industries, recognized worldwide as a leader in product qualification and compliance testing services. Elite offers the industry's most capable Electromagnetic Compatibility (EMC) testing services, including automotive EMC testing (component and whole vehicle), military EMC testing (MIL-STD-461), and commercial aviation EMC testing (RTCA DO-160). They also provide regulatory EMC & wireless testing for FCC, ISED-Canada, CE Mark, and UKCA compliance, as well as Lightning, HIRF, and High Power testing. With decades of experience, Elite's engineers provide expert technical support and utilize state-of-the-art equipment and cutting-edge test facilities. Their ISO 17025 accredited testing ensures data is accepted globally. Elite is committed to helping clients get their products to market efficiently and reliably, offering all testing services in one convenient campus location.

Website: elitetest.com

HQ: US

Countries: United States, Canada, Europe, Asia

Languages: English

Pricing model: Custom pricing

Rush Available: Yes

Standards: ISO/IEC 17025

Test Coverage: EMC only

Accredited: Yes

Max EUT Size: Large

Pre-Scan/Debug: Yes

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DNB Engineering, Inc.

DNB Engineering offers accredited EMC, EMI, HIRF, Lightning, and Environmental testing services for Aviation, Space, Defense, and other industries. They ensure product reliability and compliance with industry standards.

DNB Engineering, Inc. is a leading provider of accredited EMC (Electromagnetic Compatibility and Interference), EMI (Electromagnetic Interference), HIRF (High Intensity Radiated Fields), Direct and Induced Effect Lightning, and Environmental testing services. With over 40 years of experience, they are a recognized expert serving businesses in the Aviation, Space, Defense, Automotive, and Commercial sectors, having contributed to numerous major programs. Their comprehensive testing capabilities include Electrostatic Discharge (ESD) testing to assess equipment immunity, Environmental testing to measure performance under specified conditions and ensure product reliability, and HALT/HASS (Highly Accelerated Lifecycle Testing/Highly Accelerated Stress Screening) to identify design flaws and improve product quality before market introduction. DNB Engineering also offers Vibration testing to ensure the quality, reliability, and durability of products and components, adhering to standards like MIL-STD-810 and DO-160. They provide qualification testing services per essential standards for Aerospace, Military, Defense, Medical, and Automotive industries, helping clients achieve compliance with consumer product safety standards and bring world-class quality products to market efficiently.

Website: dnbenginc.com

HQ: Anaheim, US

Languages: English

Pricing model: Custom pricing

Lead Time: Start in 0-2 weeks

Quote SLA: 24-48 hours

Standards: ISO/IEC 17025

Test Coverage: Both

Accredited: Yes

Max EUT Size: Custom

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NTS

NTS is a global music discovery platform, broadcasting diverse genres from artists worldwide without on-air advertising. They support music culture through events and original content.

NTS is a globally recognized music discovery platform, established in 2011 by music enthusiasts for music lovers. Broadcasting from over 80 countries, NTS features a vast array of genres, from hip-hop to highlife and jungle to j-pop, all delivered without on-air advertising. The platform is committed to supporting music culture through special broadcasts, international events, and original video content produced by their in-house studio, SOUP.WORLD. NTS prioritizes human curation over algorithmic recommendations and champions freedom of expression for its radio hosts. They ensure fair compensation for artists and rightsholders through royalties and supporter subscriptions, operating in the best interests of music culture.

Website: elementdefense.com

HQ: Belcamp, United States

Countries: United States, Europe, Asia

Languages: English

Standards: ISO/IEC 17025

Test Coverage: EMC only

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QPS Evaluation Services

QPS Evaluation Services offers comprehensive testing, certification, and field evaluation for electrical and electronic products, including specialized services for medical devices, industrial equipment, and products for explosive atmospheres.

QPS Evaluation Services Inc. is a designated ATEX Notified Body and a recognized third-party testing, certification, and inspection service provider. They specialize in on-site field evaluation and certification of electrical equipment, fuel-burning appliances, and medical electrical equipment, ensuring products meet regulatory requirements for market access. With accreditations from major Canadian and US bodies, QPS facilitates product approval for North American markets and globally through schemes like IECEE/CB and IECEx. They offer a one-stop solution for safety and energy efficiency certification, including specialized services for equipment used in explosive atmospheres (IECEx Scheme) and assistance with ATEX Type Certificates. QPS also provides a Technical Advisory Service to guide clients through product development and regulatory requirements, helping to identify potential compliance issues early. Their expertise ensures a smooth and efficient path to obtaining necessary certifications and approvals, making testing and certification a satisfying experience for customers worldwide.

Website: qpsamerica.com

HQ: Toronto, Canada

Languages: English

Pricing model: Custom pricing

Standards: IEC 60601-1, IEC 60601-1-2, IEC 61010-1

Test Coverage: Both

Accredited: Yes

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Keystone Compliance

Keystone Compliance offers specialized EMC testing for medical devices, ensuring compliance with industry standards. They provide expert services to help manufacturers navigate complex regulatory requirements.

Keystone Compliance is a dedicated provider of Electromagnetic Compatibility (EMC) testing services, specifically tailored for the medical device industry. They understand the critical nature of compliance for medical equipment and offer comprehensive testing solutions to ensure devices meet stringent regulatory standards. Their expertise in EMC testing helps manufacturers identify and mitigate potential electromagnetic interference issues, which is crucial for patient safety and device reliability. By partnering with Keystone Compliance, medical device companies can streamline their product development process and gain confidence in their product's market readiness. The company focuses on delivering accurate and reliable testing results, supported by a team of experienced professionals. They are committed to assisting clients in achieving compliance with relevant national and international regulations, facilitating smoother market access for innovative medical technologies.

Website: keystonecompliance.com

HQ: US

Countries: United States, Canada, Europe, Asia

Languages: English

Standards: IEC 60601-1-2

Test Coverage: EMC only

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Applus+ Laboratories

Applus+ Laboratories offers comprehensive testing, engineering, and certification services, specializing in EMC, wireless, and electrical safety for medical device manufacturers.

Applus+ Laboratories is a leading European company providing a wide array of testing, engineering, and certification services. With extensive experience and accredited laboratories, they support manufacturers in product development and validation across various industries, including medical device EMC testing. Their expertise spans structural testing, materials testing, non-destructive testing (NDT), fire testing, and EMC, wireless, and electrical safety testing. They are equipped to handle everything from component-level analysis to full-scale product validation, ensuring compliance with international and sector-specific standards. Applus+ Laboratories is committed to enhancing product safety, quality, and reliability through rigorous testing methodologies. Their services are designed to facilitate global market access and ensure products meet the demanding requirements of regulatory bodies and industry standards.

Website: appluslaboratories.com

HQ: ES

Languages: English

Pricing model: Custom pricing

Lead Time: Start in 4-8 weeks

Quote SLA: 3-5 business days

Standards: ISO/IEC 17025

Test Coverage: Both

Accredited: Yes

Max EUT Size: Custom

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Kyrio, Inc.

Kyrio is a trusted partner for network operators and suppliers, offering comprehensive testing services for medical device EMC testing and other connectivity solutions. They ensure quality, interoperability, and a seamless user experience.

Kyrio, Inc. is a leading global partner for network innovation and connectivity, specializing in comprehensive, neutral equipment testing services, software solutions, and security services. With decades of communications technology expertise, Kyrio empowers operators to deliver strong, reliable networks and enables suppliers to confidently launch proven, certified technology. Their state-of-the-art testing lab, featuring an investment of over $20 million, is equipped with advanced tools and extensive network equipment, including anechoic chambers for antenna characterization. Kyrio provides deep technical analysis into the performance of networked devices, offering a variety of testing services such as certification, interoperability, stability, performance, compatibility, and validation testing. They also create unique, customized testing plans to meet specific customer needs. Kyrio is the authorized certification lab for all versions of CableLabs® DOCSIS® and PacketCable™ 1.5, and a trusted resource for interoperability testing. They offer specialized services including DOCSIS Pre-Testing and Wi-Fi Testing, ensuring devices meet stringent quality standards and achieve seamless interoperability. Their customer-first culture drives them to continually develop services that deliver valuable insights and a competitive advantage.

Website: kyrio.com

HQ: Louisville, US

Languages: English

Pricing model: Custom pricing

Standards: ISO/IEC 17025

Test Coverage: EMC only

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Laird Connectivity

Ezurio turns design possibility into reality with a comprehensive range of RF modules, system-on-modules, single board computers, internal antennas, IoT devices, and custom solutions. With decades of engineering expertise, Ezurio provides solutions that reduce development costs and time to market. Our global reach and unmatched support are backed by a resilient global supply chain that gives our customers the stability to overcome every design challenge with confidence. Turn design possibility into reality with Ezurio, your connectivity expert.

Ezurio, formerly known as Laird Connectivity, is a leading provider of wireless and EMC testing services, dedicated to accelerating product development and ensuring compliance for market entry. They offer expertise in various global certification standards, providing customized testing strategies and expert analysis to navigate complex regulatory requirements for products in the US, Canada, Europe, and beyond. Their services extend to comprehensive product development, including electrical & RF circuit design, custom SOM & SBC solutions, industrial design with a focus on manufacturability, and embedded software support. Ezurio's commitment to quality is underscored by their ISO 17025 and 9001 accredited wireless and EMC test laboratory, flexible laboratory space, and advanced capabilities like 3D antenna chambers. Ezurio's solutions are crucial for industries like medical devices, where longevity and regulatory compliance are paramount. They offer tailored firmware, custom enclosure designs, and modifications to form factors and connectors to meet specific application needs. With a focus on security, including secure signed firmware and vulnerability monitoring, Ezurio ensures devices are protected throughout their lifecycle. Their comprehensive approach, from prototype design to mass production and ongoing support, makes them a valuable partner for companies seeking to bring innovative and reliable products to market quickly and with reduced risk.

Website: ezurio.com

HQ: United States

Languages: English

Pricing model: Custom pricing

Standards: ISO/IEC 17025

Test Coverage: EMC only

Accredited: Yes

Max EUT Size: Custom

Pre-Scan/Debug: Yes

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GRG Metrology & Test Group Co., Ltd.

GRG Metrology & Test Group Co., Ltd. offers specialized medical device EMC testing services. They are a dedicated provider for ensuring compliance with industry standards.

GRG Metrology & Test Group Co., Ltd. is a specialized provider focused on medical device EMC testing. They offer services designed to ensure that medical devices meet stringent electromagnetic compatibility standards required for market entry and safety. Their expertise in this niche area makes them a valuable partner for manufacturers seeking to validate their products' performance and compliance. GRG Metrology & Test Group Co., Ltd. is committed to delivering reliable testing solutions tailored to the unique demands of the medical device industry.

Website: grgtest.com

Languages: English

Standards: IEC 60601-1, IEC 60601-1-2

Test Coverage: EMC only

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ICAS Testing Technology Services (Shanghai) Co., Ltd.

ICAS Testing Technology Services (Shanghai) Co., Ltd. offers specialized medical device EMC testing services. They are a key provider in Shanghai, ensuring compliance and quality for medical device manufacturers.

ICAS Testing Technology Services (Shanghai) Co., Ltd. is a dedicated provider of medical device EMC testing, operating from Shanghai. They specialize in ensuring that medical devices meet stringent electromagnetic compatibility standards, a critical aspect of product safety and regulatory approval. Leveraging their expertise, ICAS Testing Technology Services assists manufacturers in navigating the complex landscape of compliance. Their services are designed to identify and resolve potential electromagnetic interference issues, thereby enhancing product reliability and market access. As a Shanghai-based entity, they are strategically positioned to serve the growing medical device industry in the region and beyond. Their commitment to quality and precision in testing makes them a valuable partner for companies seeking to bring safe and effective medical devices to market. By focusing on EMC testing, ICAS Testing Technology Services plays a vital role in the medical device ecosystem, contributing to the overall integrity and performance of healthcare technologies.

Website: volza.com

HQ: Shanghai, China

Languages: English

Standards: IEC 60601-1-2

Test Coverage: EMC only

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Jiangsu Yangtze Testing Technology Co., Ltd.

Jiangsu Yangtze Testing Technology Co., Ltd. offers specialized medical device EMC testing services. They are a dedicated provider focused on ensuring compliance and quality for medical device manufacturers.

Jiangsu Yangtze Testing Technology Co., Ltd. is a specialized provider of medical device EMC testing services. Their focus is on ensuring that medical devices meet stringent electromagnetic compatibility standards, a critical aspect of product safety and regulatory approval. Leveraging their expertise, they assist manufacturers in navigating the complex testing landscape, ensuring their products are compliant and ready for market. This includes rigorous testing protocols designed to identify and mitigate any potential electromagnetic interference issues. Their commitment to quality and compliance makes them a valuable partner for companies in the medical device industry seeking reliable and thorough EMC testing solutions.

Website: discovery.patsnap.com

HQ: CN

Countries: United States, China, Japan

Languages: English

Standards: IEC 60601-1-2

Test Coverage: EMC only

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Hangzhou TDT Technology Co., Ltd.

Hangzhou TDT Technology Co., Ltd. specializes in medical device EMC testing, ensuring compliance with industry standards. They offer expert services for manufacturers seeking to validate their device's electromagnetic compatibility.

Hangzhou TDT Technology Co., Ltd. is a dedicated provider of specialized testing services for the medical device industry. Focusing on Electromagnetic Compatibility (EMC) testing, the company ensures that medical devices meet stringent regulatory requirements and industry standards before they reach the market. Their expertise in EMC testing is crucial for manufacturers aiming to demonstrate that their devices do not emit electromagnetic interference that could disrupt other equipment, nor are they susceptible to interference from external sources. This is particularly vital in the medical field, where device reliability and patient safety are paramount. Hangzhou TDT Technology Co., Ltd. offers comprehensive testing solutions designed to identify and resolve potential EMC issues, thereby streamlining the product development and certification process for their clients. Their commitment to quality and adherence to international standards makes them a reliable partner for medical device manufacturers globally.

Website: tdtest.cn

HQ: Hangzhou

Languages: English

Standards: IEC 60601-1-2

Test Coverage: EMC only

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Kehu-Morlab (Tianjin) Electronic Technology Co., Ltd.

Cruxi offers AI-powered regulatory submission services for medical devices, including FDA 510(k), De Novo, and PMA. They streamline compliance with expert guidance and automated checks.

Cruxi provides a comprehensive AI-powered regulatory platform designed to simplify medical device submissions for FDA and global markets. Their services cover the entire regulatory process, from device classification to final submission packages, utilizing intelligent automation and automated compliance checks. Key offerings include FDA 510(k) submissions, De Novo Classification Requests (eSTAR), Q-Submissions, and PMA Supplements. They also support 513(g) Requests and Humanitarian Device Exemptions (HDE). Cruxi aims to provide expert guidance and efficient workflows, making regulatory compliance more accessible for medical device manufacturers. The platform is built to handle various submission types, including traditional 510(k)s with a 90-day FDA review target, and supports the mandatory eSTAR use for De Novo submissions starting October 1, 2025. Their approach combines structured questioning, meeting requests, and briefing book preparation to ensure a smooth submission process.

Website: morlab.86exporter.com

HQ: Tianjin, China

Languages: English

Pricing model: Custom pricing

Standards: IEC 60601-1-2

Test Coverage: EMC only

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KSIGN Co., Ltd.

KSIGN Co., Ltd. offers specialized medical device EMC testing services, ensuring compliance with stringent industry standards. They provide expert solutions for manufacturers seeking to validate their device's electromagnetic compatibility.

KSIGN Co., Ltd. is a dedicated provider of medical device Electromagnetic Compatibility (EMC) testing. They focus on ensuring that medical devices meet the rigorous regulatory requirements for electromagnetic interference and susceptibility. Their services are crucial for manufacturers aiming to bring safe and effective medical devices to market, by validating that their products will not interfere with other devices and will not be affected by external electromagnetic fields. With a commitment to quality and compliance, KSIGN Co., Ltd. assists clients through the complex testing and certification process. Their expertise helps streamline the path to market, reducing potential delays and ensuring that devices perform reliably in their intended environments. They are a key partner for medical device innovators and established manufacturers alike, providing the necessary assurance of EMC performance.

Website: gdksign.com

HQ: United States

Languages: English

Standards: ISO/IEC 17025

Test Coverage: EMC only

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Shenzhen Academy of Information and Communications Technology

Shenzhen Institute of Information Technology (SZIIT) is a leading vocational institution specializing in Information and Communications Technology (ICT). It offers a wide range of ICT-related majors and is recognized nationally for its high-level vocational education and industry-academia collaborat

Shenzhen Institute of Information Technology (SZIIT) is a public, full-time higher education institution located in Shenzhen, China, with a strong focus on Information and Communications Technology (ICT). Established in April 2002, SZIIT has evolved into a high-level vocational institution recognized nationally for its comprehensive ICT major matrix and advanced educational practices. The institute is committed to cultivating future talent by integrating education with industry, aiming to enhance students' core competitiveness for future employment. SZIIT offers a diverse array of nearly 50 ICT-related majors, catering to over 20,000 full-time students across three-year junior college, four-year undergraduate, and postgraduate programs. It has been consistently ranked among the top vocational schools in China for teaching management, internship management, and teaching resources. SZIIT actively engages in international cooperation and has established various collaborative initiatives, including the "Bay Area Sino-German Model Base for Collaborative Development of Education and Economy." The institute is dedicated to fostering students' holistic development and preparing them to integrate into the global landscape, making it a significant player in vocational education within the region and beyond.

Website: saict.ac.cn

HQ: Shenzhen, China

Languages: English

Standards: IEC 60601-1-2

Test Coverage: EMC only

Max EUT Size: Custom

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Shenzhen BCTC Testing Co., Ltd.

Shenzhen BCTC Testing Co., Ltd. is an ISO17025 accredited laboratory providing comprehensive medical device EMC testing and certification services. They offer expertise in various international standards, including CE-RED and EN18031.

Shenzhen BCTC Testing Co., Ltd. is a professional testing and certification laboratory specializing in medical device EMC testing. As an ISO17025 accredited facility, BCTC operates in strict accordance with international quality management systems. They are recognized by CNAS and CMA, and are a cooperative laboratory with the China Quality Certification Center (CQC). BCTC offers a wide range of testing and certification services, including electrical safety testing, CE-RED, and EN18031 series testing. They are equipped to handle various international certifications such as UL, ETL, and IECEE CB Scheme. Their expertise extends to FCC certification and testing for the US market, as well as other international standards. The company emphasizes professional testing and certification, aiming to provide reliable third-party inspection reports with international credibility. They have established strategic cooperation with numerous international authoritative laboratories, including those in the US, Europe, and Canada, ensuring their test reports are globally recognized.

Website: m.bctc-test.org

HQ: Shenzhen, China

Countries: Germany, China, Canada, Japan, Europe

Languages: English

Pricing model: Custom pricing

Standards: ISO/IEC 17025

Test Coverage: Both

Accredited: Yes

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Shenzhen CTL Testing Technology Co., Ltd.

Shenzhen CTL Testing Technology Co., Ltd. offers expert EMC testing services for medical devices. They ensure compliance with regulatory standards, facilitating market access.

Shenzhen CTL Testing Technology Co., Ltd. is a specialized provider of EMC testing services, focusing on the critical area of medical devices. Their expertise ensures that medical equipment meets stringent electromagnetic compatibility standards, a crucial step for regulatory approval and market entry. Leveraging advanced testing methodologies and a deep understanding of international regulations, CTL Testing Technology helps manufacturers navigate the complex compliance landscape. Their services are designed to identify and resolve potential EMC issues early in the development cycle, saving time and resources. By partnering with Shenzhen CTL Testing Technology, companies can gain confidence in the safety and reliability of their medical devices, ensuring they perform as intended without causing or being affected by electromagnetic interference. This commitment to quality testing supports the broader goal of providing safe and effective medical solutions to the market.

Website: ctl-lab.com

HQ: Shenzhen, CN

Languages: English

Standards: IEC 60601-1, IEC 60601-1-2, IEC 60601-1-11

Test Coverage: EMC only

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International Compliance Laboratories, Inc.

Gaming Laboratories International (GLI) is a leading independent testing and certification provider for the global gaming industry. They offer comprehensive services for traditional gaming, iGaming, and lottery, ensuring regulatory compliance and product quality.

Gaming Laboratories International (GLI) is the premier independent testing and certification laboratory for the global gaming industry, established in 1989. They provide a comprehensive suite of services including pre-compliance testing, quality assurance, performance testing, and certification for a wide range of gaming products, systems, and software. GLI supports both traditional casino/property gaming and the rapidly evolving digital and iGaming sectors, including online, mobile, and interactive TV channels. Their expertise extends to jurisdictional consultation and regulatory advisory services, assisting both emerging and established markets in developing and updating technical standards. With a commitment to quality, integrity, and compliance, GLI helps clients navigate complex regulatory landscapes, accelerate market entry, and ensure product reliability. They leverage innovative testing techniques, automation, and deep industry knowledge to deliver high-quality outcomes and protect client investments across all facets of the gaming ecosystem.

Website: icl-us.com

HQ: Neenah, USA

Languages: English

Rush Available: Yes

Standards: ISO/IEC 17025

Test Coverage: EMC only

Accredited: Yes

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Element Packaging Testing

Element Packaging Testing offers expert shelf-life testing services for food, supplements, and pet products. They provide scientifically validated expiration dates, stability analysis, and microbial challenge studies to ensure product quality, safety, and regulatory compliance.

Element Packaging Testing is a global leader in providing comprehensive shelf-life testing services, crucial for maximizing product quality and extending market reach. They offer scientifically validated expiration dates for a wide range of products, including foods, supplements, and pet products, across various storage conditions (frozen, refrigerated, ambient). Their services ensure product safety, maintain quality, and meet stringent regulatory and retailer requirements. Element's expertise covers stability analysis through microbiological, chemical, and physical testing, evaluating factors like spoilage indicators, water activity, pH levels, and rancidity. They also provide specialized microbial challenge studies to identify potential spoilage risks and validate safety parameters before product launch. With a global network of over 270 ISO 17025 accredited laboratories and 8,500 experts, Element delivers tailored testing protocols and clear communication. They support R&D initiatives, validate reformulations, and verify shelf-life extensions with scientifically robust methodologies, ensuring products are safe, compliant, and fit for purpose.

Website: element.com

HQ: US

Languages: English

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F2 Labs

F2 Labs is a product compliance and certification testing lab with over 30 years of experience. They specialize in EMC, EMI, and electrical safety testing for medical devices, ensuring products meet global regulatory standards.

With over 30 years of experience, F2 Labs is a trusted partner in comprehensive product compliance and certification testing. They specialize in ensuring medical devices meet global regulatory requirements, including FCC, FDA, ISED, CE, UL, and CSA standards. F2 Labs offers expert testing services for IEC 60601-1 and IEC 60601-1-2, covering electrical safety, electromagnetic compatibility (EMC), and electromagnetic interference (EMI). Their services ensure products operate as intended in their intended environment and do not interfere with other devices, crucial for patient safety and market access. Beyond testing, F2 Labs provides expert consulting to guide clients through the entire product certification process. They are equipped to test a wide range of electrical products, from battery chargers to medical electrical equipment and wireless devices, providing reliable results with precision and efficiency. Clients praise their responsiveness, thoroughness, and ability to guide them through complex certification processes.

Website: f2labs.com

HQ: Location Testing, US

Languages: English

Standards: IEC 60601-1, IEC 60601-1-2, IEC 60601-1-2 Ed. 4

Test Coverage: Both

Max EUT Size: Custom

Pre-Scan/Debug: Yes

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PSN Labs

PSN Labs is a full-service engineering partner specializing in medical device EMC testing, design, development, and manufacturing. They offer end-to-end solutions from concept to market, ensuring product safety and regulatory compliance.

PSN Labs is a comprehensive engineering partner with a strong focus on the medical device industry, offering specialized services in EMC testing, design, development, and manufacturing. Their state-of-the-art Testing Laboratory is ISO/IEC 17025:2017 accredited, ensuring accurate and reliable data for a wide range of material and product testing needs. They provide end-to-end engineering services, guiding products from initial concept through to market launch, with a particular emphasis on biocompatibility and toxicology. With an ISO 13485 certified engineering lab, PSN Labs is equipped to handle the entire product realization process, from early-stage design to final validation. They offer customized testing solutions, including custom test method development, functional device testing, and design verification testing, often collaborating with their accredited test lab. Their expertise extends to material science, helping clients select and process materials for optimal performance and safety, and they are adept at navigating complex regulatory landscapes, including FDA submissions and 510(k) clearance. PSN Labs prides itself on being more than just a testing facility; they are a development partner that provides in-depth analysis and realistic solutions. Their team of material scientists, toxicologists, and engineers work collaboratively to solve complex design, material, and manufacturing challenges, ensuring devices meet both performance and regulatory requirements. They are committed to patient safety and regulatory compliance, making them a trusted resource for medical device manufacturers.

Website: psnlabs.com

HQ: Erie, US

Languages: English

Pricing model: Custom pricing

Standards: ISO/IEC 17025

Test Coverage: Both

Accredited: Yes

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IMR Test Labs

IMR Test Labs offers accredited materials testing services for medical device manufacturers and suppliers. They specialize in ensuring material quality, biocompatibility, and compliance with industry standards to mitigate patient health risks.

IMR Test Labs is an accredited materials testing laboratory with over 20 years of experience serving the medical device and dental industries. They provide comprehensive analytical services to ensure the quality and safety of medical devices, including implants, surgical instruments, and coatings. Their expertise helps manufacturers and suppliers meet rigorous OEM standards, mitigate patient health risks associated with contaminants, and ensure devices are manufactured to precise specifications. Specializing in areas like medical cleanliness testing and coatings analysis, IMR Test Labs performs a variety of tests, including in vitro evaluations to assess potential toxic effects without risk to animals or humans. This contributes to determining overall biocompatibility and identifying contaminants. Their services are crucial for validating the viability of permanent implants and minimizing post-surgery complications by verifying medical cleanliness. IMR Test Labs is a preferred testing partner for leading manufacturers across various industries, including medical devices. They hold ISO 17025 and Nadcap accreditations, underscoring their commitment to quality control and process management. With multiple locations in the US and internationally, they are well-equipped to support the complex testing needs of the medical device sector.

Website: imrtestlabs.com

HQ: Lansing, US

Languages: English

Pricing model: Custom pricing

Quote SLA: < 24 hours

Rush Available: Yes

Standards: ISO/IEC 17025

Test Coverage: EMC only

Accredited: Yes

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tricor-systems.com

Website: tricor-systems.com

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haapd.com

Website: haapd.com

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Element U.S. Space & Defense

Element U.S. Space & Defense, formerly NTS, offers accredited testing and engineering services for aerospace, defense, and commercial compliance. Specializing in EMC/EMI, environmental simulations, and ballistics.

Element U.S. Space & Defense, formerly known as NTS, is a trusted government testing partner established in 1961. They provide a comprehensive suite of accredited testing and engineering services for mission-critical programs across aerospace, defense, and commercial sectors. Their expertise includes environmental simulations, EMI/EMC testing, dynamics, hydraulics, ballistics, and ordnance testing. With multiple state-of-the-art laboratories across the US, they are equipped to verify product readiness for real-world use and accelerate time to market. Element U.S. Space & Defense holds numerous accreditations, including ISO/IEC 17025, NVLAP, and approvals from agencies like the Defense Logistics Agency, ensuring compliance with rigorous industry standards. They are a Space Flight Awareness Supplier Award winner, committed to technical excellence and meeting demanding scheduling requirements.

Website: nts.com

HQ: Fullerton, US

Languages: English

Pricing model: Custom pricing

Lead Time: Start in 4-8 weeks

Quote SLA: 3-5 business days

Standards: ISO/IEC 17025

Test Coverage: Both

Accredited: Yes

Max EUT Size: Custom

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NU Laboratories, Inc.

NU LABS offers comprehensive EMI/EMC testing services for military and commercial applications. They specialize in environmental simulation, noise, shock, and vibration testing.

NU LABS, established in 1962, provides high-quality environmental and EMI/EMC testing services for industry, military, and government clients. They specialize in dynamic, high-intensity noise, EMI, and environmental simulation testing, ensuring fast turnaround and meticulous attention to detail. Their extensive equipment is continuously updated to maintain a competitive edge. Services include Temperature, Solar Radiation, Wind and Rain, Enclosure Effectiveness, Spraytight, Watertight, Drip-proof, Solvent Resistance, Dielectric Strength, Hydrostatic Pressure Testing, Flow Testing, Explosive Decompression, Solderability, EMC Testing, and Electrostatic Discharge. NU LABS is committed to supporting client testing programs with superior service and expertise. Located at 312 Old Allerton Road, Annandale, NJ 08801, NU LABS is equipped with a Vibration Table up to 5500 lbs and an Electrodynamic Shaker up to 10,000 LBF, alongside high-speed photography and video capabilities.

Website: nulabs.com

HQ: Annandale, US

Languages: English

Pricing model: Custom pricing

Quote SLA: 24-48 hours

Standards: IEC 60601-1, IEC 60601-1-2, IEC 61010-1

Test Coverage: Both

Max EUT Size: Custom

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GlobalCompliance Solutions Pro

Leading global regulatory compliance consultancy serving medical device manufacturers worldwide with comprehensive regulatory services.

Website: globalcompliance-solutions.com

HQ: Boston, US

Jurisdictions: EU, UK, US

Countries: DE, FR, GB, US

Languages: English, French, German, Spanish

Response SLA: 24 hours

Onboarding time: 7–30 days

Pricing model: Custom pricing

Lead Time: Start in 2-4 weeks

Quote SLA: 24-48 hours

Rush Available: Yes

Standards: IEC 60601-1, IEC 60601-1-2, IEC 61010-1

Test Coverage: Both

Accredited: Yes

Pre-Scan/Debug: Yes

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MedReg International Pro

Specialized regulatory consultancy providing end-to-end compliance solutions for medical devices, IVDs, and combination products across all major markets.

Website: medreg-international.com

HQ: London, UK

Jurisdictions: EU, UK, US

Countries: DE, FR, GB, US

Languages: English, French, German, Spanish

Response SLA: 24 hours

Onboarding time: 7–30 days

Pricing model: Custom pricing

Lead Time: Start in 2-4 weeks

Quote SLA: 24-48 hours

Rush Available: Yes

Standards: IEC 60601-1, IEC 60601-1-2, IEC 61010-1

Test Coverage: Both

Accredited: Yes

Pre-Scan/Debug: Yes

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Regulatory Excellence Partners Pro

Boutique regulatory consultancy offering personalized, high-touch regulatory services for innovative medical device companies and startups.

Website: regulatoryexcellence.com

HQ: San Francisco, US

Jurisdictions: EU, UK, US

Countries: DE, FR, GB, US

Languages: English, French, German, Spanish

Response SLA: 24 hours

Onboarding time: 7–30 days

Pricing model: Custom pricing

Lead Time: Start in 2-4 weeks

Quote SLA: 24-48 hours

Rush Available: Yes

Standards: IEC 60601-1, IEC 60601-1-2, IEC 61010-1

Test Coverage: Both

Accredited: Yes

Pre-Scan/Debug: Yes

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Comprehensive Buyer's Guide

1. Who Needs EMC Laboratory & Electrical Safety Testing?

Medical electrical equipment (ME equipment) must demonstrate compliance with IEC 60601-1 (electrical safety)^[1] and IEC 60601-1-2 (EMC)^[2] before market placement in most jurisdictions. EMC laboratories and electrical safety testing labs provide the required testing services.

This requirement applies to:

Medical devices with electrical functions — any device that uses electricity for diagnosis, treatment, or monitoring requires testing at an EMC laboratory or electrical safety testing lab^[1]
Active medical devices — devices that depend on a source of energy other than that generated by the human body or gravity^[1]
Devices for FDA 510(k) submission — electrical safety and EMC testing from accredited emc testing labs are typically required for premarket submissions^[4]
Devices for CE marking (EU MDR) — compliance with IEC 60601 series tested at electromagnetic compatibility laboratories is required for medical electrical equipment^[5]
Home healthcare equipment — may require additional testing per IEC 60601-1-11 at specialized emc test laboratories^[6]

Note: Even if your device is battery-powered or low-voltage, it may still be considered medical electrical equipment and require testing at an accredited EMI testing lab or emc laboratory. Consult with a testing laboratory or regulatory expert to determine applicability.

References

IEC 60601-1:2012+AMD1:2020 CSV — Medical electrical equipment — Part 1: General requirements for basic safety and essential performance (International Electrotechnical Commission (IEC)) — 2020-08-20
IEC 60601-1-2:2014+AMD1:2020 CSV — Medical electrical equipment — Part 1-2: General requirements for basic safety and essential performance — Collateral Standard: Electromagnetic disturbances — Requirements and tests (International Electrotechnical Commission (IEC)) — 2020-08-20
FDA — Recognized Consensus Standards — Medical Devices (U.S. Food and Drug Administration) — 2024-01-01
FDA — Premarket Notification 510(k) (U.S. Food and Drug Administration) — 2024-01-01
Regulation (EU) 2017/745 (MDR) — Annex I — General safety and performance requirements (European Union) — 2017-04-05 — Annex I
IEC 60601-1-11:2015+AMD1:2020 CSV — Medical electrical equipment — Part 1-11: General requirements for basic safety and essential performance — Collateral Standard: Requirements for medical electrical equipment and medical electrical systems used in the home healthcare environment (International Electrotechnical Commission (IEC)) — 2020-08-20

2. What Services Are Typically Included?

Electrical Safety + EMC testing services typically include:

IEC 60601-1 electrical safety testing: Comprehensive testing of basic safety and essential performance requirements^[1], including electrical hazards, mechanical safety, and risk management verification
IEC 60601-1-2 EMC testing: Electromagnetic compatibility testing including emissions (conducted and radiated)^[2] and immunity (ESD, EFT, surge, RF immunity, dips/interruptions)^[2]
Test planning and protocol development: Development of test plans based on device characteristics and intended use
Test execution: Performance of tests in accredited facilities with proper chamber calibration and measurement equipment^[3]
Test reports: Comprehensive test reports suitable for regulatory submissions, including test conditions, results, and compliance statements
Pre-scan/debugging services (optional): Early-stage testing to identify EMC issues before formal testing, reducing time and cost
Retest support: Engineering support and retesting if initial tests reveal non-compliance

Additional services may include:

Particular standard testing (IEC 60601-2-x series for specific device types)
Home healthcare environment testing (IEC 60601-1-11)^[6]
CB Scheme testing and certification
On-site testing for large or immobile equipment
Wireless/RF testing add-on services

References

IEC 60601-1:2012+AMD1:2020 CSV (International Electrotechnical Commission (IEC)) — 2020-08-20
IEC 60601-1-2:2014+AMD1:2020 CSV (International Electrotechnical Commission (IEC)) — 2020-08-20
ISO/IEC 17025:2017 — General requirements for the competence of testing and calibration laboratories (International Organization for Standardization (ISO)) — 2017-11-01
IEC 60601-1-11:2015+AMD1:2020 CSV (International Electrotechnical Commission (IEC)) — 2020-08-20

3. What Affects Pricing?

Pricing for electrical safety + EMC testing varies based on several factors:

Test scope: Safety only, EMC only, or both — complete packages (safety + EMC) are typically more cost-effective than separate testing
Device complexity: Number of applied parts, operating modes, and test configurations — more complex devices require more test time and documentation
Standards required: Base standards (IEC 60601-1, IEC 60601-1-2) vs. additional particular standards (IEC 60601-2-x) or collateral standards (IEC 60601-1-11)^[1]^[6]
EUT size and weight: Larger devices may require special handling, larger chambers, or on-site testing — all of which can increase costs
Wireless capabilities: Devices with radios (Bluetooth, Wi-Fi, cellular) may require additional RF testing and coexistence evaluation
Use environment: Home healthcare environment testing (IEC 60601-1-11)^[6] adds complexity and cost compared to professional healthcare environments
Accreditation requirements: Accredited testing (ISO/IEC 17025)^[3] may cost more but is required for regulatory submissions in most markets
Lead time: Rush services (testing within 2-4 weeks) typically cost 20-50% more than standard lead times (4-8 weeks)
Pre-scan/debugging: Optional pre-scan services can help identify issues early but add to total project cost
Retest needs: If initial tests reveal non-compliance, retesting and engineering support add to total cost

Typical pricing ranges:

EMC testing only: $10,000 - $25,000 for standard medical devices
Safety testing only: $15,000 - $35,000 depending on complexity
Complete package (Safety + EMC): $20,000 - $50,000+ for standard devices
Complex devices or rush services: $50,000 - $100,000+

Tip: Request quotes from multiple laboratories and compare not just price, but also lead times, accreditation status, and included services. Accredited test reports are essential for regulatory submissions.

References

IEC 60601-1:2012+AMD1:2020 CSV (International Electrotechnical Commission (IEC)) — 2020-08-20
IEC 60601-1-11:2015+AMD1:2020 CSV (International Electrotechnical Commission (IEC)) — 2020-08-20
ISO/IEC 17025:2017 (International Organization for Standardization (ISO)) — 2017-11-01

4. How to Choose an EMC Laboratory or Electrical Safety Testing Lab

When selecting an EMC laboratory, electrical safety testing lab, or electromagnetic compatibility laboratory, consider these factors:

Accreditation status: Verify ISO/IEC 17025 accreditation^[1] and review the accreditation scope document to ensure your specific standards and test methods are covered — accredited test reports from emc testing labs are required for most regulatory submissions
Standards coverage: Confirm the emc laboratory can test to the specific standards you need (IEC 60601-1, IEC 60601-1-2, particular standards, etc.)^[2]^[3]
Test coverage: Determine if you need safety only, EMC only, or both — some emc test laboratories specialize in one area, while others offer complete packages
EUT capacity: Verify the EMI testing lab can accommodate your device size, weight, and power requirements — check chamber dimensions and maximum EUT specifications
Lead time and availability: Compare lead times (standard vs. rush) and availability windows — some emc labs have 8-12 week backlogs, while others can start in 2-4 weeks
Regulatory acceptance: Confirm test reports from the electromagnetic compatibility laboratory are accepted by your target regulatory authorities (FDA, EU notified bodies, etc.) — accredited emc testing labs generally provide reports suitable for multiple markets
Pre-scan/debugging support: If you're new to EMC testing or have had issues before, consider emc test houses that offer pre-scan services to identify problems early
Wireless/RF capabilities: If your device has radios, verify the emc laboratory can test wireless functionality and coexistence
On-site testing: For large or immobile equipment, confirm if on-site testing is available and what the additional costs are
Response time and communication: Check quote response SLAs and communication quality — fast, clear communication is essential for project success
Pricing transparency: Look for emc testing labs that provide detailed quotes with clear breakdowns of included services, exclusions, and potential additional costs

Red flags: EMC laboratories that cannot provide accreditation scope documents, vague pricing without detailed breakdowns, unrealistic lead times, or lack of experience with medical devices.

References

ISO/IEC 17025:2017 (International Organization for Standardization (ISO)) — 2017-11-01
IEC 60601-1:2012+AMD1:2020 CSV (International Electrotechnical Commission (IEC)) — 2020-08-20
IEC 60601-1-2:2014+AMD1:2020 CSV (International Electrotechnical Commission (IEC)) — 2020-08-20

5. How Cruxi Quotes Work

Getting quotes through Cruxi is simple and fast:

Submit one request: Fill out a single form with your device details, testing requirements, standards needed, target markets, timeline, and budget
Routed to Pro laboratories: Your request is automatically sent to Pro testing laboratories that match your requirements (typically 3-5 laboratories)
Compare quotes: Receive detailed quotes directly from laboratories and compare pricing, lead times, capabilities, and included services

Benefits:

Save time by avoiding individual laboratory outreach
Compare multiple options side-by-side
Pro laboratories respond fastest (typically within 24-48 hours)
No obligation to accept any quote
Access to accredited laboratories with proven track records

Alternative: You can also request quotes directly from individual laboratories via their profile pages.

6. Listed vs Claimed vs Pro

Status	Meaning	RFQ Routing
Pro	Laboratory is Pro and opted in to receive RFQs	Included in multi-quote requests; responds fastest
Claimed	Laboratory has claimed their profile but is not Pro for RFQ routing	Direct requests only; not in multi-quote routing
Listed	Laboratory listed from public sources; profile not claimed	Manual contact required; not guaranteed to respond

Recommendation: For fastest response times and best quote comparison, prioritize Pro laboratories when requesting multiple quotes.

7. Onboarding Checklist (What Laboratories Typically Ask For)

To get accurate quotes and start testing efficiently, laboratories typically request:

Device information: Device name, model number, intended use, classification, and regulatory pathway (510(k), CE marking, etc.)
Technical specifications: Power requirements (battery/mains/both), dimensions, weight, operating modes, and applied parts
Standards needed: Specific IEC 60601 standards required (IEC 60601-1, IEC 60601-1-2, particular standards, etc.)^[1]^[2]
Target markets: Where you plan to market the device (US, EU, UK, etc.) — this affects which standards and test methods are required
Use environment: Home healthcare, professional healthcare, or industrial — affects test requirements (e.g., IEC 60601-1-11 for home use)^[3]
Wireless capabilities: If the device has radios (Bluetooth, Wi-Fi, etc.), specify types and bands
Sample readiness: When samples will be available and how many units you can provide
Timeline: Desired start date and any hard deadlines (e.g., regulatory submission deadline)
Prior test data: Any previous test reports or pre-compliance testing results (if available)
Attachments: Device specifications, block diagrams, user manuals, or other relevant documentation

Tip: More complete information leads to more accurate quotes and faster project kickoff. If you're unsure about any requirements, use the "Help me scope" option in the RFQ form.

References

IEC 60601-1:2012+AMD1:2020 CSV (International Electrotechnical Commission (IEC)) — 2020-08-20
IEC 60601-1-2:2014+AMD1:2020 CSV (International Electrotechnical Commission (IEC)) — 2020-08-20
IEC 60601-1-11:2015+AMD1:2020 CSV (International Electrotechnical Commission (IEC)) — 2020-08-20

Frequently Asked Questions

Q1: What is an EMC laboratory and what do they test?

An EMC laboratory (also called emc lab, electromagnetic compatibility laboratory, or emc testing lab) is an accredited testing facility that performs electromagnetic compatibility testing on medical devices and other electronic equipment. EMC laboratories test two main areas: emissions (how much electromagnetic energy your device emits) and immunity (how well your device functions when exposed to electromagnetic disturbances). For medical devices, emc testing labs typically test to IEC 60601-1-2^[1]. Many EMC laboratories also offer electrical safety testing (IEC 60601-1) and are accredited to ISO/IEC 17025^[2]. When searching for 'emc labs near me' or 'emc testing labs near me', verify the laboratory's accreditation scope covers your specific testing needs.

References

IEC 60601-1-2:2014+AMD1:2020 CSV (International Electrotechnical Commission (IEC)) — 2020-08-20
ISO/IEC 17025:2017 (International Organization for Standardization (ISO)) — 2017-11-01

Q2: What is the difference between IEC 60601-1 and IEC 60601-1-2?

IEC 60601-1 addresses electrical safety and essential performance requirements for medical electrical equipment^[1], including protection against electrical hazards, mechanical safety, and risk management. IEC 60601-1-2 addresses electromagnetic compatibility (EMC)^[2], including emissions (how much electromagnetic energy the device emits) and immunity (how well the device functions in the presence of electromagnetic disturbances). Most medical electrical equipment requires testing to both standards at an accredited EMC laboratory or electrical safety testing lab for regulatory compliance.

References

IEC 60601-1:2012+AMD1:2020 CSV (International Electrotechnical Commission (IEC)) — 2020-08-20
IEC 60601-1-2:2014+AMD1:2020 CSV (International Electrotechnical Commission (IEC)) — 2020-08-20

Q3: What is the difference between an EMC lab and an EMI testing lab?

EMC (Electromagnetic Compatibility) and EMI (Electromagnetic Interference) are closely related terms. An EMI testing lab typically focuses on measuring electromagnetic interference/emissions from devices, while an EMC laboratory or emc test laboratory performs both emissions testing and immunity testing (how devices respond to electromagnetic disturbances). For medical devices, most emc test houses and electromagnetic compatibility laboratories offer comprehensive testing to IEC 60601-1-2^[1], which includes both EMI/emissions and immunity requirements. When requesting quotes, clarify whether you need emissions only, immunity only, or complete EMC testing. Most accredited emc testing labs offer full-service testing packages.

References

IEC 60601-1-2:2014+AMD1:2020 CSV (International Electrotechnical Commission (IEC)) — 2020-08-20

Q4: Do I need both safety and EMC testing, or can I do just one?

Most medical electrical equipment requires both safety (IEC 60601-1)^[1] and EMC (IEC 60601-1-2)^[2] testing for regulatory compliance. However, some emc laboratories and electrical safety testing labs offer testing to individual standards if you only need one. For example, if you've already completed safety testing elsewhere, you might only need EMC testing at an emc test laboratory. Confirm with your regulatory team and target markets which tests are required. Most emc testing labs offer package deals for complete testing (safety + EMC) that are more cost-effective than separate testing.

References

IEC 60601-1:2012+AMD1:2020 CSV (International Electrotechnical Commission (IEC)) — 2020-08-20
IEC 60601-1-2:2014+AMD1:2020 CSV (International Electrotechnical Commission (IEC)) — 2020-08-20

Q5: What is ISO/IEC 17025 accreditation and why does it matter?

ISO/IEC 17025 is the international standard for testing and calibration laboratory competence^[1]. Accreditation to ISO/IEC 17025 demonstrates that an EMC laboratory, electrical safety testing lab, or emc test laboratory has the technical competence, quality management system, and measurement traceability to perform specific tests reliably. Accredited test reports from emc testing labs are generally required for regulatory submissions in most markets (FDA 510(k), CE marking, etc.). When requesting quotes from emc laboratories or electrical safety testing labs, ask for their accreditation scope document to verify they're accredited for your specific standards and test methods (IEC 60601-1, IEC 60601-1-2, etc.).

References

ISO/IEC 17025:2017 (International Organization for Standardization (ISO)) — 2017-11-01

Q6: How long does IEC 60601 testing typically take?

Testing timelines vary based on device complexity, test scope, and laboratory capacity. Typical timelines: EMC testing only: 3-4 weeks from sample receipt; Safety testing only: 4-6 weeks; Complete package (Safety + EMC): 6-10 weeks. Rush services (2-4 weeks) are available at most laboratories but typically cost 20-50% more. Factors affecting timeline include: device complexity (more test configurations = longer testing), retest needs (if initial tests reveal issues), laboratory backlog, and report preparation time. Plan for 8-12 weeks total project time (including sample shipping, testing, and report delivery) for standard lead times.

Q7: What is pre-scan/debugging and do I need it?

Pre-scan/debugging is optional early-stage EMC testing performed before formal compliance testing. It helps identify EMC issues (emissions or immunity problems) early, allowing you to fix them before expensive formal testing. Pre-scan services are particularly valuable if: you're new to EMC testing, you've had EMC issues in the past, your device has complex electronics or wireless capabilities, or you want to reduce the risk of retesting. While pre-scan adds to project cost, it can save significant time and money by avoiding retests. Many laboratories offer pre-scan as an optional service.

Q8: Can I use the same test report for FDA 510(k) and CE marking?

In many cases, yes — test reports from accredited laboratories testing to IEC 60601-1 and IEC 60601-1-2^[1]^[2] are generally accepted by both FDA (for 510(k) submissions)^[3] and EU notified bodies (for CE marking under MDR)^[4]. However, confirm with your regulatory team and testing laboratory, as some markets may have specific requirements or test method variations. Accredited test reports from ISO/IEC 17025-accredited laboratories^[5] are typically the most widely accepted.

References

IEC 60601-1:2012+AMD1:2020 CSV (International Electrotechnical Commission (IEC)) — 2020-08-20
IEC 60601-1-2:2014+AMD1:2020 CSV (International Electrotechnical Commission (IEC)) — 2020-08-20
FDA — Recognized Consensus Standards (U.S. Food and Drug Administration) — 2024-01-01
Regulation (EU) 2017/745 (MDR) — Annex I (European Union) — 2017-04-05 — Annex I
ISO/IEC 17025:2017 (International Organization for Standardization (ISO)) — 2017-11-01

Q9: What if my device fails testing?

If your device fails initial testing, most laboratories offer retest support and engineering consultation to help identify and fix issues. Common failure modes include: EMC emissions exceeding limits (requiring shielding or filtering), EMC immunity failures (requiring better circuit design or protection), or safety issues (requiring design changes). Laboratories typically provide detailed failure analysis and recommendations. You'll need to: fix the issues, potentially retest specific areas, and pay for retesting (usually at a reduced rate). Pre-scan/debugging services can help identify issues early and reduce the risk of formal test failures.

Q10: Do I need IEC 60601-1-11 testing for home-use devices?

If your medical electrical equipment is intended for use in the home healthcare environment, you may need additional testing per IEC 60601-1-11^[1]. This collateral standard addresses specific safety and performance requirements for devices used by lay users in non-clinical environments. Requirements include: usability considerations, environmental conditions (temperature, humidity, power quality variations), and instructions for use. Confirm with your regulatory team and testing laboratory whether IEC 60601-1-11 applies to your device. Many laboratories offer IEC 60601-1-11 testing as an add-on service.

References

IEC 60601-1-11:2015+AMD1:2020 CSV (International Electrotechnical Commission (IEC)) — 2020-08-20

Q11: What should I include in an RFQ to get accurate quotes?

To get accurate, comparable quotes, include: Device details: name, type, dimensions, weight, power requirements; Standards needed: specific IEC 60601 standards (IEC 60601-1, IEC 60601-1-2, particular standards); Test scope: safety only, EMC only, or both; Target markets: US, EU, UK, etc.; Use environment: home, professional healthcare, or industrial; Wireless capabilities: if applicable, radio types and bands; Timeline: desired start date and any hard deadlines; Sample availability: when samples will be ready and how many units; Budget range: to help laboratories provide appropriate options. Attach device specifications, block diagrams, or user manuals if available.

Q12: What is the 4th edition of IEC 60601-1-2 and do I need it?

The 4th edition of IEC 60601-1-2 (published in 2014, amended in 2020) is the current version of the EMC standard^[1]. Earlier editions (2nd and 3rd) are still recognized in some markets but are being phased out. For new devices and regulatory submissions, you should test to the 4th edition. Some laboratories may offer testing to older editions for legacy devices or specific market requirements, but confirm with your regulatory team. When requesting quotes, specify "IEC 60601-1-2 Ed. 4" to ensure you're getting quotes for the current standard.

References

IEC 60601-1-2:2014+AMD1:2020 CSV (International Electrotechnical Commission (IEC)) — 2020-08-20

Provider Comparison Table

Provider	Accredited	Primary Standards	Test Coverage	Wireless Add-on	Lead Time	Quote SLA	Rush	Max EUT Size	Chamber Type	Pre-Scan/Debug	Regions Served	Languages	Response SLA
UL Solutions	No	IEC 60601-1-2	Both	No	—	—	No	—	—	No	—	English	Request quote
Intertek	No	IEC 60601-1-2	EMC only	No	—	—	No	—	—	No		English	Request quote
TÜV SÜD	Yes	IEC 60601-1, IEC 60601-1-2, IEC 60601-1-11	Both	Yes	Start in 2-4 weeks	3-5 business days	Yes	Large	Semi-anechoic	Yes	Europe, North America, Asia	English	3-5 business days
TÜV Rheinland	No	IEC 60601-1	Both	No	—	—	No	—	—	No	—	English	Request quote
SGS	No	IEC 60601-1-2	EMC only	No	—	—	No	—	—	No	—	English	Request quote
CSA Group	No	IEC 60601-1, IEC 60601-1-2, IEC 61010-1	Both	No	—	—	No	Custom	—	No	US Northeast Corridor, US Southeast Corridor, Caribbean	English	Request quote
Nemko	Yes	IEC 60601-1-2	EMC only	No	Start in 4-8 weeks	3-5 business days	No	—	—	No	Global	English	3-5 business days
DEKRA	Yes	IEC 60601-1-2	EMC only	No	Start in 4-8 weeks	3-5 business days	Yes	—	—	No	Global	English	3-5 business days
Element Materials Technology	Yes	ISO/IEC 17025	Both	No	Start in 4-8 weeks	3-5 business days	No	Custom	Anechoic	No	U.S. Government, Military, Aerospace	English	3-5 business days
Bureau Veritas	Yes	IEC 60601-1, IEC 60601-1-2, IEC 60601-1-11	Both	Yes	Start in 4-8 weeks	3-5 business days	Yes	Large	Semi-anechoic	No	Americas, Europe, Asia Pacific	English	3-5 business days

Sources & Official Guidance

Official sources vary by directory. See the applicable regulation and competent authority guidance for this role.

Last Updated: 2026-02-04

Reviewed by: Cruxi Regulatory Affairs Team

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Comprehensive Buyer's Guide

1. Who Needs EMC Laboratory & Electrical Safety Testing?

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2. What Services Are Typically Included?

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3. What Affects Pricing?

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4. How to Choose an EMC Laboratory or Electrical Safety Testing Lab

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5. How Cruxi Quotes Work

6. Listed vs Claimed vs Pro

7. Onboarding Checklist (What Laboratories Typically Ask For)

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Frequently Asked Questions

Q1: What is an EMC laboratory and what do they test?

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Q2: What is the difference between IEC 60601-1 and IEC 60601-1-2?

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Q3: What is the difference between an EMC lab and an EMI testing lab?

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Q4: Do I need both safety and EMC testing, or can I do just one?

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Q5: What is ISO/IEC 17025 accreditation and why does it matter?

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Q6: How long does IEC 60601 testing typically take?

Q7: What is pre-scan/debugging and do I need it?

Q8: Can I use the same test report for FDA 510(k) and CE marking?

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Q9: What if my device fails testing?

Q10: Do I need IEC 60601-1-11 testing for home-use devices?

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Q11: What should I include in an RFQ to get accurate quotes?

Q12: What is the 4th edition of IEC 60601-1-2 and do I need it?

References

Related Regulatory Services

Provider Comparison Table

Sources & Official Guidance