SaMD ISO 13485 Consultants

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

Global Regulatory Compliance Experts. Since 1978, Lachman Consultants has offered compliance, regulatory affairs, and technical services to pharmaceutical, medical device, and biologics clients worldwide.

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

RQM+: FDA Regulatory Consulting for MedTech & Software Expertise

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

Freyr Solutions – Expert FDA Regulatory Consulting for Medical Devices

FDA 510(k) & De Novo Consulting for Medical Device Startups | DocLab Inc.

FDA 510(k) Consulting for SaMD & Digital Health Devices | 12 Years Experience | US & EU Client Focus

Expert Regulatory Services for Drugs, Biologics, and Devices

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

Global Quality & Regulatory Executive | 41 Yrs MedTech | FDA, EU MDR, ISO | 130+ Class II/III Approvals |...

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

Regulatory Compliance Associates (RCA) – FDA 510(k) & regulatory consulting

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

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

FDA Regulatory Consultant | 510(k), De Novo, PMA | SaMD, Imaging, Digital Health

FDA 510(k) Regulatory Consulting Firm

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

Regulatory Compliance Associates – FDA Regulatory Consulting for Medical Devices

Expert FDA Regulatory Guidance for Medtech - 510k, De Novo, PMA & More

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

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

MedTech Regulatory & Project Leader | Combination Products | 510(k) & EU MDR | QMS & Validation Expert

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

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

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

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

FDA 510(k) Regulatory Consulting Expert

Seasoned Global Quality & Regulatory Executive | Medical Devices | FDA Submissions, QMS & EU MDR Expert

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.

To optimize patient care and improve outcomes, Innovenn works to build patient-centered SaMD digital health solutions

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

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 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

Medical Device Regulatory Affairs & QA Consultant | 4+ Yrs Exp | FDA 510(k) Submissions | Startups

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.

25+ Yrs MedTech Leader: Regulatory, Clinical, Product Dev, AI, SaMD, Cybersecurity. Global Approvals.

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

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

Regulatory Affairs Professional | 4+ Yrs Exp | 510(k), De Novo, Clinical Trials | Biologics & Medical Devices

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.

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

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

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

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

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

Senior Regulatory Affairs Leader | Combination Products | Digital Health | Global Submissions

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

Expert FDA & EU MDR Regulatory Strategist | Quality Systems Specialist | Global Market Access

Expert in Regulatory Information Management (RIM) & Innovation | FDA/Global Compliance | System Analysis & Optimization