Medical Device CE Mark & Quality System Certification: Recent & Proposed Changes 2016
20 Oct 2016
Webinar
Description
Topics
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
Who should Attend
Attendees from:
Manufacturing & Design Engineers
Quality & Regulatory Professionals
Program Managers
Marketing Product Managers
Past Events
Medical Device CE Mark & Quality System Certification: Recent & Proposed Changes 2016 - 20 Oct 2016, Webinar (62921)
Important
Please, check "Medical Device CE Mark & Quality System Certification: Recent & Proposed Changes" official website for possible changes, before making any traveling arrangements
