How to Create A PMS Plan and Report According to EU MDR 2017/745 Article 83-86?
Website https://www.complianceonline.com/pms-eu-mdr-2017-745-webinar-training-706533-prdw?channel=Ourglocal |
Edit Freely
Category
Deadline: July 05, 2020 | Date: July 15, 2020
Venue/Country: U.S.A
Updated: 2020-06-24 19:30:55 (GMT+9)
Call For Papers - CFP
The new medical device regulation EU MDR 745/2017 in the European Union has a lot of new requirements. One hot topic is the focus on the "Post-Market- Surveillance-Process" and the new requirements e.g. reporting to Competent Authorities and Notified Bodies and how this process is connected to other processes in the quality management system according to ISO 13485:2016. The understanding of these changes and how to implement changes until May 2021 is essential to keep your certificates and to keep the market entry open.Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
Disclaimer: ourGlocal is an open academical resource system, which anyone can edit or update. Usually, journal information updated by us, journal managers or others. So the information is old or wrong now. Specially, impact factor is changing every year. Even it was correct when updated, it may have been changed now. So please go to Thomson Reuters to confirm latest value about Journal impact factor.