Join us on Wednesday, January 25th at 2:00 PM Eastern as LNE/G-MED North America Inc. will be hosting a free informative session on the MEDDEV 2.7.1 Rev 4: New Requirements and Changes for Clinical Evaluation Reports (CER).
In June 2016, the MEDDEV 2.7.1 rev 4, the European guidance on the clinical evaluation of medical devices (MD) was published. The issuance of this guidance happened shortly after the publication of the text of the future Regulation on the Medical Device (MDR) of 15 June 2016, which anticipates many new requirements for clinical evaluation. Although, the MEDDEV 2.7.1 rev 4 does not revolutionize the approach on Clinical Evaluation, it does significantly increase the demands on the content of the file... Click here to READ MORE!
Topic: MEDDEV 2.7.1 Rev 4: New Requirements and Changes for Clinical Evaluation Reports (CER)
Date: Wednesday, January 25th, 2017
Time: 2:00 - 2:30 PM Eastern Standard Time
Presenter: Anne Le Rouzo, West Coast Regional Director & Certification Project Manager at LNE/G-MED North America, Inc. Click here to Register!