Medical Device Reporting Requirements for Manufacturers Final Guidance 2017

  • 16 May 2017
  • Webinar

Description

Medical Device Reporting Requirements for Manufacturers Final Guidance 2017 is a webinar that covers topics such as:

  • Reporting requirements
  • MDR regulation
  • Written procedures
  • Manufacturer reporting requirements
  • Specific issues and situations
  • Recordkeeping and public disclosure
  • Report timing
  • Malfunction reporting
  • When do you "become aware?"

Medical Device Reporting Requirements for Manufacturers Final Guidance 2017 is intended for attendees involved or interested in:

  • Regulatory Affairs
  • Clinical Affairs
  • R&D
  • Quality
  • Consultants
  • Complaint and Risk Management Personnel
  • Contractors/subcontractors
  • Senior Management
  • Other interested parties

Past Events

Important

Please, check "Medical Device Reporting Requirements for Manufacturers Final Guidance" official website for possible changes, before making any traveling arrangements

Event Categories

Health & Medicine: Medical device

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