Medical Device Single Audit Program [MDSAP] Implementation & Participating Country Regulatory Processes: U.S., Canada, Brazil, Australia and Japan

Medical Device Single Audit Program [MDSAP] Implementation & Participating Country Regulatory Processes: U.S., Canada, Brazil, Australia and Japan is a seminar that covers topics such as:

  • Device Classification
  • The Medical Device Single Audit Program (MDSAP)
  • Medical Device GMP
  • Licensing Pathways
  • Device Labeling
  • Inspections
  • Timelines and Fees
  • License Holder Responsibilities
  • Adverse Event Reporting
  • Country Specific Cultural Considerations and Challenges

Medical Device Single Audit Program [MDSAP] Implementation & Participating Country Regulatory Processes: U.S., Canada, Brazil, Australia and Japan brings together attendees from:

  • Quality assurance, quality control, and quality systems
  • Regulatory Affairs
  • Contract research organizations
  • Product development personnel
  • Site managers
  • Business management
  • Contractors and subcontractors
  • Senior and executive management
  • Consultants
  • Distributors

Important

Please, check the official conference website for possible changes, before you make any traveling arrangements

Prices are for evaluation only.

Other Events with Similar Categories

Other Events with Similar Location or Organizer