ABOUT THE WEBINAR
Join us for an in-depth webinar addressing the challenges of transitioning from the Medical Device Directive (MDD/AIMDD) to the Medical Device Regulation (MDR) focusing on biological safety. Obtain valuable insights into MDR requirements, avoid common pitfalls and streamline the preparation and submission of your MDR documentation.Our expert speakers will provide general guidance on conformity assessment for biocompatibility, reprocessing, sterile packaging, and both standard and non-standard sterilization methods. You can gain a clear understanding of the key differences between the MDD and MDR in these areas, as well as the documentation expectations of Notified Bodies.In the second half, join an engaging panel discussion featuring Notified Body representatives. This interactive session is your opportunity to deepen your knowledge and ask our panel any burning question you may have.
WEBINAR TOPICS
- Biocompatibility
- Reprocessing
- Sterile packaging Sterilization
- Questions and answers
SPEAKERS
- Dr. Johannes König
Manager Global Accounts in-vitro Diagnostics (IVD), TÜV SÜD - Dr. Dominik Reitermayer
Expert for Reprocessing, TÜV SÜD - Dr. Mark Smith
Expert for Sterilization, TÜV SÜD - Dr. Stefanie Boellner
Expert for Biocompatibility, TÜV SÜD - Dr. Trixi Hollweck
Expert for Packaging, TÜV SÜD - Pia Burscheidt
Expert for Sterilization, TÜV SÜD
