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