The Global Value for Clinical Evaluation Reports in Medical Device Studies

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.

• Sandra Welch, Director of Clinical Research Services, NAMSA