Sufficient Clinical Data in the Transition from the MDD to the EU MDR

Sufficient Clinical Data in the transition from the MDD to the EU MDR

View On-Demand Webinar

View On-Demand Webinar


The Regulation (EU) 2017/745 (MDR) is in force since May, but there are still open questions related to the definition of sufficient clinical data for medical devices.

This webinar will provide information on the transition from the MDD to the MDR, focusing on legacy medical devices. This will include an overview of the clinically relevant MDCG guidance documents and the requirements to collect clinical data in the post-market setting.

Complete the form to view the on-demand webinar!

Topics covered in the webinar:

  • Clinical data
  • Current MDCG
  • Guidance documents
  • PMCF requirements
  • Legacy medical devices

About the speaker

Matthias Fink, M.D.

Clinical Focus Team Manager North America, TÜV SÜD America 

Board certified orthopedic and trauma surgeon with 17 years of experience in orthopedic, trauma and reconstructive surgery and extensive training in cardiovascular and thoracic surgery. Working for TÜV SÜD Product Service in Germany since 2016 as a Clinical Reviewer in the Clinical Centre of Excellence before joining TÜV SÜD America in 2017. Senior Clinical Expert Orthopedic Surgery for the Clinical Centre of Excellence and the Team Manager of the Clinical Focus Team North America.

He participates as a presenter at national and international conferences and workshops on the clinical requirements and the implementation of the EU MDR.

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