ComplianceOnline

Critical Examination of MED/DEV 2.12/2 Rev 2 On Post-Market Clinical Follow-Up Studies

  • By: Haroon Atchia, CEO & Technical Director, Quality First International
  • Date: May 01, 2013
Webinar All Access Pass Subscription Abstract:

In this article, Haroon Atchia, CEO & Technical Director of Quality First International provides a critical examination of the European Commission's update of MEDDEV 2.12/2 entitled Post Market Clinical Follow-Up Studies, a guide for Manufacturers and Notified Bodies, published in January 2012.

Bookmark and Share
Best Sellers
You Recently Viewed
    Loading