Share Your Research, Maximize Your Social Impacts
Main Menu
Searching By
PARTNERS
2021 - Medical Device Single Audit Program [MDSAP] Implementation & Participating Country Regulatory Processes: U.S., Canada, Brazil, Australia and Japan
Date2021-08-11
Deadline2021-08-01
VenueVirtual Seminar, 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
Inspections
Device Labeling
License Holder Responsibilities
Timelines and Fees
Country Specific Cultural Considerations and Challenges
Adverse Event Reporting
Device Classification
Licensing Pathways
Medical Device GMP
Inspections
Device Labeling
License Holder Responsibilities
Timelines and Fees
Country Specific Cultural Considerations and Challenges
Adverse Event Reporting
Other CFPs
- 21 CFR Part 11 Compliance for SaaS/Cloud Applications
- Reduce costs for compliance with data integrity: 21 CFR Part 11, SaaS/Cloud, EU GDPR
- Family & Medical Leave Act, the Families First Coronavirus Response Act, and the American Rescue Plan Act: What Employers Need to Know in 2021
- Payroll Disaster Recovery what we learned from the COVID pandemic
- In Plain Sight: Finding and Eliminating Organizational Inefficiencies
Last modified: 2021-07-07 14:38:12