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Session 20: Post-NDA Approval Regulatory Requirements
Session Chair(s)
Michael Hamrell, PhD, RAC
President
MORIAH Consultants, United States
- Post-NDA Approval Obligations
- Postmarketing (Phase 4) Requirements and Commitments
- Supplements and other Changes to an Approved Application
- Postmarketing Reporting of Adverse Drug Experiences
- 15-Day Alert Reports
- NDA Annual Reports
- NDA Field Alert Reports
- Biologic Product Deviation Reports
- Drug Registration and Listing
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