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Medical devices regulations – preparing and prioritising

Brussels 20 January 2017

  • Introduction
  • Definitions, scope of application and classification rules
  • Notified bodies
  • Q&A with panel
  • IVD Regulation (IVDR)
  • General Regulation : clinical evidence requirements,traceability, vigilance and post-market surveillance
  • General Regulation : liabilities
  • Brexit and the Regulations
  • Q&A with panel and conclusion

Pharma Compliance Digital CRM Marketing Transparence DMOS Brussel January 20th 2017 Medical devices regulations  –  preparing and prioritising

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