Medical Device Single Audit Program [MDSAP] Implementation & Participating Country Regulatory Processes 2017

  • 12-13 Oct 2017
  • Courtyard Arlington Crystal City / Reagan National Airport, VA, United States

Description

Topics
  • 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
Who should Attend

All personnel in the Medical Device industry.

Past Events

Important

Please, check "Medical Device Single Audit Program [MDSAP] Implementation & Participating Country Regulatory Processes" official website for possible changes, before making any traveling arrangements

Event Categories

Education: E-learning, Education Technologies & Methods, Higher education, Preschool , Primary and Secondary Education, Training
Health & Medicine: Medical device, Medical laboratories, Medical technology

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