Upcoming Events
Pharmaceutical / Medicinal
OCT
14
SCOPE
SCOPE Europe: Summit for Clinical Ops Executives 2025 Step into the future of clinical operations excellence at CHI's 8th Annual SCOPE Europe: Summ ...
14 - 15 Oct 2025
Barcelona, Spain
OCT
23
IVC 2025
5th Edition of International Vaccines Congress Get ready for the 5th Edition of the International Vaccines Congress (IVC 2025), taking place ...
23 - 25 Oct 2025
Orlando, United States
OCT
27
Food as Medicine Policy Summit The ninth edition in the series overall, and second annual Food as Medicine Policy and Resear ...
27 - 28 Oct 2025
Virginia, United States
NOV
11
PEGS Europe: Protein & Antibody Engineering Summit 2025 Network with 1,500+ colleagues at the largest protein & antibody engineering event in Eur ...
11 - 13 Nov 2025
Lisbon, Portugal
NOV
11
Drug Discovery Chemistry Europe 2025 Drug Discovery Chemistry is a dynamic conference and networking event for drug discovery scie ...
11 - 13 Nov 2025
Barcelona, Spain
JUN
12
ICPPS 2026
2026 11th International Conference on Pharmacy and Pharmaceutical Science (ICPPS 2026) Publication: 1. International Journal of Applied Pharmaceutics (IJAP, ISSN: 0975 C7058), whi ...
12 - 15 Jun 2026
Bali, Indonesia
JUN
22
TRADITIONALMED
9th Edition of International Conference on Traditional Medicine and Integrative Health Magnus Group presents the 9th Edition of International Conference on Traditional Medicine and ...
22 - 24 Jun 2026
Barcelona, Spain
JUN
24
MEDCHEM-2026
2nd World Summit on Medicinal Chemistry and Drug Delivery (MEDCHEM-2026) You are invited to speak at the 2nd World Summit on Medicinal Chemistry and Drug Delivery (ME ...
24 - 26 Jun 2026
, Italy

Dec
15

Lead Auditor EN ISO 13485:2016 and EU MDR 2017/745 - Regulation

 
 Seminar/trade show (noCPF)

When:

  15 Dec 2020 through 16 Dec 2020

Where:

  Online Event | United States

Website URL:

  https://www.complianceonline.com/en-iso-13485-2016-eu-mdr-2017-745-seminar-training-80654SEM-prdsm?channel=Brownwalker

Categories:

  Medicine & Health - Pharmaceutical / Medicinal

Keywords:


Event description:

The new medical device regulation EU MDR 745/2017 in the European Union has a lot of new requirements. This new upcoming regulation is also stronger connected to the EN ISO 13485:2016. The understanding of this changes and how to implement last minute changes until May 2021 is essential to keep your certificates. The first key for the understanding and the implementation of the changes is the knowledge about the interfaces between the EN ISO 13485:2016 and the EU MDR 2017/745. The second key is to understand, which parts of the EU MDR 2017/745 are not covered by the EN ISO 13485:2016. These not covered paragraphs and requirements must be additional implemented into the quality management system until May 2020. The time is short and immediately action is required. Learning Objectives : Introduction, who must apply the new EU MDR 2017/745 requirements? Overview about the changes of the EU MDR 2017/745 regarding quality management What are the interfaces between the EN ISO 13485:... Read more

Posting date:

27 November 2020  |  426 views

Placement:

Not-featured (How do I make my event featured?)