IVD Consultants

Assistance to initial importer and distributors

Full-Service CRO | FDA 510(k) & PMA Expert | Medtech Design, Regulatory & Commercialization

FDA 510(k), De Novo, PMA Consulting for Medical Devices by Emergo by UL

MCRA – Expert FDA Regulatory Consulting for Medical Devices

NAMSA: FDA 510(k) Regulatory Consulting Expert | 15 Years Experience | Global Support

RQM+: FDA Regulatory Consulting for MedTech & Software Expertise

FDA Compliance Group LLC offers FDA registration support, SOP development, FDA-483 and Warning letter responses, mock FDA inspections, gap analysis, and compliance training. Former FDA employees helping regulated industries achieve and maintain compliance.

FDA 510(k) Consulting & Accredited Third Party Reviewer | 12 Years Experience

ICON plc – Expert FDA 510(k) & Medical Device Regulatory Consulting

FDA 510(k) Regulatory and Quality Consulting Firm - 12 Years Experience

Expert FDA 510(k) Regulatory Consulting for Medical Devices

i3cglobal: Expert FDA 510(k) & Regulatory Strategy Consulting for Medical Devices

Medical Device Regulatory Expert | 25+ Years Experience | FDA, EU MDR, Risk Management, 510(k), ISO 14971

Expert FDA Regulatory Consulting for Medtech: 510k, De Novo, PMA

Regulatory Affairs Strategy Director | 15+ Yrs Global Medtech & IVD Compliance | FDA Clearances & Crisis Management

de novo jury consulting: Expert FDA Regulatory Strategy for De Novo, 510(k), and PMA Submissions

Expert FDA 510(k) Regulatory Consulting Firm | Global Testing & Training

RadUnity Corp.: Expert FDA Regulatory Guidance for Medical Device Innovators | 11+ Years Experience

FDA 510(k) Regulatory Consulting Firm

Fang Consulting – FDA Regulatory & QMS Expert for Medical Devices

Expert QA/RA Director | MedTech Product Launch | FDA, EU-MDR, MDSAP | QMS & Validation Specialist

FDA 510(k) Regulatory Consulting Firm | QMS | Class I & II Devices

Expert FDA 510(k) Regulatory Consultant specializing in Ultrasound and Implant Devices | 20 Years Experience

Regulatory Affairs Expert with 2+ Years of MedTech Experience - Enhancing Compliance for Medical Devices

Translational Medicine & Regulatory Affairs Executive | 15+ Years | Drugs, Biologics, Devices, IVDs

Elexes – Expert FDA 510(k) & Regulatory Consulting for Medical Devices

Certified QA/RA Leader | 22+ Yrs Life Sciences | QMS, MDSAP, FDA, EU MDR | eQMS & Digital Compliance Expert

Senior FDA Regulatory & IVD Consultant | 30+ Years Experience | 510(k), De Novo, EUA Expert | Inventor of...

Expert FDA 510(k) Regulatory Consulting | Medical Device Academy

HP&M – FDA 510(k) & regulatory consulting

FDA 510(k) Regulatory Consulting Expert

Fang Consulting, Ltd. – FDA 510(k) & regulatory consulting | Quality Assurance | Risk Management

Leavitt Partners: Expert FDA Regulatory Consulting for MedTech Innovation

Fda510kconsulting offers expert 510(k) submission services, guiding medical device manufacturers through the FDA approval process for the US market.

Qmlogic offers specialized 510(k) submission services, guiding medical device companies through the FDA regulatory process to achieve market clearance.

Global Regulatory Partners (GRP) offers end-to-end regulatory affairs, clinical, quality, and pharmacovigilance services for medical devices, pharmaceuticals, cosmetics, and nutraceuticals. FDA U.S. Agent, 510(k) submission, PMA, regulatory strategy, and Q-Sub meeting support.

FDA 510(k) Regulatory Consulting for Global Medical Device Manufacturers - IVD Specialist

Expert SaMD & AI/ML Regulatory Strategist | FDA 510(k), PMA, EU MDR/IVDR | 8+ Years Experience

FDA 510(k) Regulatory Consulting Expert | Medical Devices | Provision Consulting Group

Cruxi provides expertise in FDA QSR/QMS transition inspection readiness, ensuring compliance with regulatory requirements.

Expert FDA Regulatory Compliance Consultant | QMS, Audits, 510k, PMA, Global Submissions | 15+ Yrs Exp.

30 Years FDA Regulatory & QA Expertise | 510k, PMA, QMS, Audits | Radiology, IVD, Orthopedic

Expert FDA Regulatory & Clinical Consultant | Driving Medtech Innovation from Strategy to Submission.

ELS Group is a company with deep technical expertise and market access in Regulatory Affairs and Quality Assurance, duly certified. With 18 years of experience, we provide strategic solutions.

Expert in Drug Discovery, Medical Devices (IVDR), and Regulatory Affairs with 15+ years experience

Ph.D. Scientific & Regulatory Consultant | Biomedical Expertise | Big Data Analysis | FDA Regulatory Affairs

Regulatory professional with expertise in EU MDR/IVDR & FDA compliance for medical devices, IVDs, and pharmaceuticals.

RAC-certified Regulatory Affairs professional with 7+ years of global experience in Class I, II, and III medical devices and IVDs, including software-enabled and digital medical devices.

Regulatory Affairs Expert - Medtech Compliance & Strategy

Expert FDA Regulatory Reviewer with 10+ years at FDA, specializing in IVDs, risk assessment, and pathway strategy.

35+ year RA/QA expert & ex-Notified Body Auditor specializing in global submissions (FDA, EU MDR, MDSAP) & QMS for...

Global Quality & Regulatory Affairs Leader | FDA & International Compliance | QMS Expert | Device & Combination Products

25+ Years QA/RA Leadership: FDA & Intl. Submissions, Inspections, Medical Devices & Comb. Products

20-Year Medtech Quality & Regulatory Executive | Medical Device & IVD Expert

Expert Regulatory Affairs Consultant | 20+ Yrs PMA, IDE, 510(k), EU MDR | Global Strategy & Approvals

Expert QMS & ISO 14971 Risk Management Pro | EU MDR, SaMD, IVD Compliance | 10+ Yrs MedTech Experience

Expert Regulatory Affairs Leader | Global Approvals | Devices, Biologics, Gene Therapies | FDA & EMA Navigation

Medical Device Regulatory & Clinical Affairs Expert | 30+ Yrs Exp | FDA Submissions | Global Approvals | QMS

IQVVV MedTech solutions are purpose-built for the medical device and diagnostics industry, spanning the entire product lifecycle from strategy and portfolio analysis to post-market.