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Medical Device CE Mark & Quality System Certification: Recent & Proposed Changes 2016

Medical Device CE Mark & Quality System Certification: Recent & Proposed Changes 2016 will be held on October 20, 2016.

 

Medical Device CE Mark & Quality System Certification: Recent & Proposed Changes 2016 is a webinar that covers topics such as:

  • IVD, MDD & Active Implantable Directive
  • New approach directives & background
  • Competent Authorities & Notified Bodies
  • Impact of significant recent & proposed changes
  • Device classification
  • Medical Device Directive vs. Regulation vs. ISO 13485
  • Technical files vs. Guidance Documents
  • Routes to CE marking under various MDD annexes
  • Essential requirements

 

Medical Device CE Mark & Quality System Certification: Recent & Proposed Changes 2016 is intended for attendees from:

  • Manufacturing & Design Engineers
  • Quality & Regulatory Professionals
  • Program Managers
  • Marketing Product Managers