Medical Device Single Audit Program [MDSAP] Implementation & Participating Country Regulatory Processes: U.S., Canada, Brazil, Australia and Japan 2019

  • 07-08 Feb 2019
  • Jersey City, NJ, United States

Description

Medical Device Single Audit Program [MDSAP] Implementation & Participating Country Regulatory Processes: U.S., Canada, Brazil, Australia and Japan 2019 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 2019 brings together:

  • 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

Past Events

Important

Please, check "Medical Device Single Audit Program [MDSAP] Implementation & Participating Country Regulatory Processes: U.S., Canada, Brazil, Australia and Japan" official website for possible changes, before making any traveling arrangements

Event Categories

Health & Medicine: Medical device, Medical technology
Science: Health sciences
Technology: Biotechnology, Information Technology (IT)

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