Companies related to MDSAP

Medical Device Certification

We provide conformity assessment services (certification, testing, audit, inspection) for a broad range of products.

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

Medical device quality and regulatory services you can count on

“Your trusted global end-to-end solution partner in medical device regulatory affairs and compliance."

We thrive on partnering with clients in highly-regulated industries 🏥💊🚙✈️ to deliver innovative compliance solutions.

Leading the Global Excellence in Orthodontic Manufacturing🦷✨

Global Medtech Clinical, Regulatory, Reimbursement, Compliance & Quality Consultancy

Are you a start-up medical device company that needs help preparing an FDA 510k submission, quality system, or training?

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

Compliance services for medical devices and aerospace

Manufacturers of Nonwoven Medical Disposables || CE MDR Certified || MDSAP Certified || ISO 13485 Certified

Sharing Knowledge + Expertise in Quality Management

Changing lives, one brain at a time!

Quality and Compliance Consulting | Regulatory Compliance Audits | Quality Management System | Risk Management

Global consultants w/+100 years of experience w/in biotechnology, medical device, pharmaceutical, & clinical diagnostics

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 !

Focused on solutions

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