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Clinical Evaluations & Investigations

Clinical strategies: Are you EU MDR compliant?

Clinical Evaluations & Investigations Highlights Include:

Everything you need to know about the new clinical evidence requirements
  • What are Competent Authorities looking for from industry? Find out...
  • Clarifying Notified Body interpretation of MDR clinical evidence requirements
  • Exactly what is “sufficient” clinical data?
  • Get to grips with the new process for class III implantables
  • Assessing the increased requirements for Clinical Evaluation Reports (CERs)

Competent Authority, Notified Body and industry perspectives from:
  • TÜV SÜD Product Service
  • Philips
  • MED-EL Medical Electronics

We’ll answer your biggest clinical and regulatory questions

Join our interactive panel discussions addressing:

  • The implications of the MDR on data management
  • Gaining regulatory approval for software devices
  • Best practices for conducting a clinical investigation under the MDR

On-Demand Clinical Content

Clinical Webinars

High-Quality Real-World Clinical Data to Support Medical Device and Pharmaceutical Post-Mark Clinical Follow-ups

Dr. Vivian Tian, Business Development Manager – EU and US, 1MData