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Whitepaper

MDR Clinical Evaluation Seminar and Workshop

QUNIQUE presents its seminar and workshop ‘Medical Device Regulation (MDR) Performing Successful Clinical Evaluation’, which will take place on the 11 January 2018 in Zurich Hilton Hospital.

Key topics will include:

  • Clinical requirements of medican device directives (MDD) versus MDR
  • The clinical evaluation process
  • Following good clinical practice (GCP)
  • Post-market clinical follow-up (PMCF) requirements and how to plan accordingly

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MDR Clinical Evaluation Seminar and Workshop

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