Companies related to IVDR

Connected.Committed to Community.

GMED est un organisme de certification et un organisme notifié français en Europe (numéro d’identification 0459).

Effortlessly navigate the medical device approval processes and market and quickly market your device world-wide.

For safety and quality

For safety and quality

Authorized Representative - EC REP / CH-REP / UK Responsible Person / U.S. Agent / Australian TGA Sponsor

Better Bioinformatics For Everyone!

Let's Do Engineering

Regulatory, Quality Assurance and Clinical Affairs Experts for the medical device and life science industries

Regulatory, Quality Assurance and Clinical Affairs Experts for the medical device and life science industries

Swiss Medical Technology Association

On a mission to improve lives by providing tech-enabled, culturally relevant translation solutions in any language.

Excellence in Clinical Evaluation, Clinical Investigation, PMS/PMCF and Medical Affairs

Literature Search Experts Focused on Delivering the Highest Caliber Literature Review, Clinical Evaluation and PMS

European Association for Persons Responsible for Regulatory Compliance

Your Clinical and Regulatory Partner for MDR, IVDR, and Beyond. Clinical Trials | MDR & IVDR Compliance | XcelTrials EDC

New input output under regulation

DNA-based products, oligonucleotides, CE IVD kits, GMP/GLP services

Your Consultant in Israel for Medical Device & Cosmetic Global Regulations

Your Vision Meets Our Expertise: Advancing Medical Devices and SaMD for Optimal Patient Care

Creamos/adaptamos tu dossier técnico a MDR, IVDR "transformando problemas en soluciones". consultoria@a3zadvanced.com

Our Mission - Targeted Procurement of Human Biospecimens

Medical Devices 🩺 In vitro diagnostic medical devices 🦠 Personal protective equipment (PPE) 😷 Certification process

Providing platforms and diagnostic solutions to bridge the gap from research to market

The Most Comprehensive AI Enabled RIMS For MedTech Companies

Modern and dynamic Life Sciences experts, that delivers regulatory certainty and confidence in your compliance

Accelerate your path to market with our global team of MedTech experts.

Engineering for healthcare innovation globally

Clinical regulatory writing, advice, and strategy for registration and compliance of state-of-the-art medical devices.

Medical device and IVD Regulatory Affairs, Clinical Affairs & Quality Assurance Consultancy services

Hands-on specialist services for MedTech: regulatory strategy, QMS, data and market insight, training. CH-REP services.

Right First Time | Regulatory Experts | MedTech | Cosmetics | Medicines | ISO 13485 | MDSAP | Clinical | Medical Writing

MedTech QA/RA eLearning | ISO Standards | Auditing | Multi-Accredited Transformational Training

Helping Medical Device companies with EUDAMED Compliance - Software - Training - Support - Consultancy - EUDAMED App

Medical Device and IVD Expertise | Consulting firm | Clinical Research and Regulatory Affairs | MedTech Experts

Your contract research organization specialized in medical devices

Focused on solutions

The only unified AI-powered RIM software that was purpose-built for MedTech teams, by regulatory experts.

MedTech Market Research | Post Market Surveys

HealthTech Innovators Support: Regulatory, Reimbursment, Clinical, and Business Development.

The medical devices manufactured by our clients are know for their safety, reliability and quality for their users.

Partnering with MedTech companies to achieve compliance and success—while improving patient outcomes.

The Innovation CRO

We cover the full range of regulatory services to medical devices and IVDs at any point in the product lifecycle.

The assistance of medical technologies development from idea to the market is our passion !

We help you to gain, and retain, regulatory compliance in a competitive marketplace.

Your partner in immunotechnologies since 1980! Our commitment makes the difference!

Tailored CRO. MedTech Focus. Precision in Clinical, Regulatory & Certification.

QA/RA Medical Device & IVD Consultancy UKRP - QMS - MDR - IVDR - ISO 13485 - CE Marking - Global Submissions - UKCA

"One-Point Solution" for all your medical device / IVDs.

We help brands grow, launch, and stand out by combining strategy, science, and storytelling into one powerful solution.

Your Regulatory Specialist

GDP Experts: Ensuring Compliance with Precision

Streamlining Global Medical Device Compliance: EUDAMED, GUDID, SWISSDAMED, SFDA, MHRA, TGA & More #UDI

We integrate Regulatory, Clinical and Quality requirements with global medical product lifecycle success.