Loading, Please Wait...

Products & Services

Hours of Operation Closed now

  • Saturday 09:00 AM - 06:00 PM
  • Sunday 09:00 AM - 06:00 PM
  • MondayClosed
  • TuesdayClosed
  • WednesdayClosed
  • ThursdayClosed
  • FridayClosed

10006 Cross Creek Blvd. Suite 71 10006 Cross Creek Blvd. Suite 71, Tampa, FL 33647

https://www.compliancequest.com/regulations/what-is-eu-mdr/

CQ-eu mdr - Introduction

EU MDR (The European Union Medical Device Regulation) is a regulatory framework that applies to all European medical device manufacturers to establish high quality and safety standards for medical devices production.

Products & Services

  • CQ-eu mdr

    In the modern world, the life sciences sector is going through a period of unprecedented regulatory change affecting organizations involved in pharmaceuticals, medical devices, and in-vitro diagnostics. The European Union Medical Device Regulation (EU MDR), a robust, transparent, predictable and sustainable regulatory framework for medical devices, ensures high standards of quality and safety being produced in or supplied into Europe.

Customer Reviews: 0 Votes / 0 Reviews

  • Be the first to rate.

Contact Details

Contact us

Manage Your Profile
Is your business listed correctly on America’s largest city directory network of 1,000 portals? Find your City Portal