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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

Mark Cusworth, VP Research and Development, PRISYM ID
Andrew Love, VP Capability Development, Be4ward

Latest status and practical experience of implementing the new EU MDR

Bassil Akra, Vice President, Global Focus Teams (Cardiovascular, Orthopeadic and Clinical), TÜV SÜD Product Service GmbH, Germany