CE Marking for Medical Devices Including In Vitro Diagnostic Devices - Webinar By GlobalCompliancePanel 2012

  • 09 Aug 2012
  • Webinar

Description

CE Marking for Medical Devices Including In Vitro Diagnostic Devices is a webinar that covers topics such as:

  • Overview of European Medical Device Regulations and Regulatory Framework for Medical Devices
  • How EU laws are made
  • Active Implantable Medical Device Directive (AIMDD)
  • Medical Device Directive (MDD)
  • The directive amending MDD and AIMDD
  • In Vitro Diagnostic Device Directive (IVDD)
  • ISO 13485, ISO 14155, and ISO 14971
  • CE marking principles
  • GHTF and MEDDEV guidance documents

CE Marking for Medical Devices Including In Vitro Diagnostic Devices brings together:

  • Clinical Affairs Managers, Directors and VPs
  • Regulatory Affairs Managers, Directors and VPs
  • Quality Managers, Directors and VPs
  • Quality Managers, Directors and VPs
  • Sales and Marketing Managers, Directors, and VPs
  • Compliance Managers and Directors
  • Site Managers, Directors, and Consultants
  • Complaint Handling and Risk Management Managers and Directors
  • Compliance Officers and Legal Counsel
  • Senior and Executive Management
  • Business Development Managers, Directors, and VPs

Past Events

Important

Please, check "CE Marking for Medical Devices Including In Vitro Diagnostic Devices - Webinar By GlobalCompliancePanel" official website for possible changes, before making any traveling arrangements

Event Categories

Health & Medicine: Medical device, Medical laboratories, Pharma

Other Events with Similar Categories

Other Events with Similar Location or Organizer

Featured Conferences & Exhibitions