The “new” Medical Device Regulation has been in effect since 26 May 2021. At our digital business brunch, we will discuss the resulting changes to national legislation and interactions with the GDPR, as well as the official guidelines from the expert panel. We will also discuss relevant questions about transitional rules and periods in accordance with Article 120 of the MDR and its impact on the distribution of devices conforming to the Directive.
Session 1: MDR follow-up
- National legislation
- MDCG guidelines
Session 2: Deep dive: transitional periods
- Article 120 of the MDR
- Conformity and declarations of conformity still in accordance with the MDD?
Session 3: The MDR and the GDPR
- Commonalities and differences with regard to patient data and protection of data relating to health
- Miriam Schuh, Head of Healthcare
Register now. Participation is free of charge for clients, SMEs, industry players, etc. but subject to a fee for external consultants. For participation in the event, we charge € 599.00 (net) payable within 14 days after registration. If you would like to participate as an external consultant, please contact firstname.lastname@example.org.
The event will be conducted as a webinar with Zoom video conferencing software on 19 November 2021 from 10:30 am-12:00 pm.back