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.

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

Better Bioinformatics For Everyone!

Let's Do Engineering

For safety and quality

For safety and quality

Swiss Medical Technology Association

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

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

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

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

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

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

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

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

New input output under regulation

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

European Association for Persons Responsible for Regulatory Compliance

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

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

Your contract research organization specialized in medical devices

Our Mission - Targeted Procurement of Human Biospecimens

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

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

Engineering for healthcare innovation globally

The Most Comprehensive AI Enabled RIMS For MedTech Companies

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

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

MedTech Market Research | Post Market Surveys

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

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

Focused on solutions

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

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

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

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

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

The Innovation CRO

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

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!

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

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

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

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

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 !

Your Regulatory Specialist

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