The Cutting Edge of Medical Technology Content, Community & Collaboration
Time: February 29, 2016 from 9am to 10am
Location: Online
Website or Map: http://xtalks.com/Clinical-Ev…
Event Type: free, webinar
Organized By: Xtalks Life Science Webinars
Latest Activity: Jan 29, 2016
The European Commission Guidance MEDDEV 2.7.1 rev. 3 Clinical Evaluation: Guide for Manufacturers and Notified Bodies provides details on the process of conducting clinical evaluations and the requirements for creating a Clinical Evaluation Report. The document also provides a list of references that can be useful.
In this webinar, the speaker will examine the requirements listed in MEDDEV 2.7.1 rev. 3 while focusing on the global benefits of the Clinical Evaluation report for an individual's product’s path to market.
© 2025 Created by CC-Conrad Clyburn-MedForeSight. Powered by
RSVP for Free Webinar: The Global Value for Clinical Evaluation Reports in Medical Device Studies to add comments!
Join MedTech I.Q.