Regulation 2023/607 was published in March 2023, extending MDD validity by up to 5 years. Join our webinar to learn about the impact on conformity assessment and marketing authorization of this regulation.
Objective
The objective of this webinar is to present regulation 2023/603 and the associated Q&A document released by the EU Commission as well as the associated opportunities and constraints for manufacturers and their way to compliance with MDR(EU) 2017/745 requirements.
Agenda
- Introduction
- Regulation 2023/607
- Q&A documents
- What manufacturer can and can’t do?
- How can SGS support your strategy?
- Q&A
Target Audience: This webinar is aimed at medical device manufacturer management teams, including quality or regulatory affairs managers.
Can’t make a live session? Register now here.
