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2021 - Medical Device Single Audit Program [MDSAP] Implementation & Participating Country Regulatory Processes: U.S., Canada, Brazil, Australia and Japan



VenueVirtual Seminar, USA - United States USA - United States

KeywordsGMP audit; Mdsap audit; Device classification


Topics/Call fo Papers

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

Last modified: 2021-07-07 14:38:12