The new medical device regulation EU MDR 745/2017 in the European Union has a lot of new requirements. This new regulation is also stronger connected to the EN ISO 13485:2016. The understanding of this changes and how to implement 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 since May 2021. The EU Commission publish monthly new guidance documents for deeper understanding of the requirements and to give more clarification about the expectations by authorities and notified bodies.
You should attend this webinar to understand, what are the changes to the previous medical device regulation and how to implement the changes in your current quality management system in a simple and quick way. This need smart ideas to reach the right level to pass the quality management audit by your certification company or notified body.
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 13485:2016 and the EU MDR 2017?
- Which new requirements of the EU MDR 2017/745 are not covered by the EN ISO 13485:2016?
- Smart and fast ways to implement the changes in your quality management system
- Fast track internal audit to approve the changes
Areas Covered :
- The new scope of the EU MDR 2017/745
- The obligations and roles of the EU MDR 2017/745
- How work the regulation and the EN ISO 13485:2016 together?
Who will Benefit:
CEO’s, product manager, quality/ regulatory / medical affairs manager, quality representatives of
- medical device manufacturer,
- importer,
- distributors
- dealers
