EU Medical Device Law
We can help answer your legal questions related to the EU MDR
2018 Highlights Include:
Finding solutions for every legal challenge
- Come to terms with new liability rules and how they may impact you
- Enhance your knowledge on the Person Responsible for Regulatory Compliance
- Do you understand the legal status of Notified Bodies under the MDR?
- Get to grips with recent case law related to the EU MDR
- How will the General Data Protection Regulation (GDPR) impact you?
In-house counsel and private practice perspectives
- Agfa HealthCare
- Biovotion AG
- Agilent Technologies
- White & Case LLP
- Simmons & Simmons
- Morgan, Lewis & Bockius LLP
Insightful debates and discussions…
We’ll be hosting interactive panel discussions on:
- Experiences with implementing the EU MDR in practice
- Experiences with preparing for requirements of the GDPR
- Open floor Q&A session
Free On-Demand Content
Webinars. Webinars. Webinars.
EU MDR Labeling Compliance: Learn the Lessons from UDI
Speakers:
Mark Cusworth, VP Research and Development, PRISYM ID
Andrew Love, VP Capability Development, Be4ward
WATCH THIS WEBINAR
Latest status and practical experience of implementing the new EU MDR
Speaker:
Bassil Akra, Vice President, Global Focus Teams (Cardiovascular, Orthopeadic and Clinical), TÜV SÜD Product Service GmbH, Germany
WATCH THIS WEBINAR