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

Let's Do Engineering

Better Bioinformatics For Everyone!

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

Your Consultant in Israel for Medical Device & Cosmetic Global Regulations

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

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

New input output under regulation

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

European Association for Persons Responsible for Regulatory Compliance

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

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

Our Mission - Targeted Procurement of Human Biospecimens

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

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

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

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

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

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

The Most Comprehensive AI Enabled RIMS For MedTech Companies

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

Your contract research organization specialized in medical devices

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

MedTech Market Research | Post Market Surveys

The Innovation CRO

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

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

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

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

Focused on solutions

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

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

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

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

Engineering for healthcare innovation globally

Your Regulatory Specialist

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

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

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

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

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

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

GDP Experts: Ensuring Compliance with Precision

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

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

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

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