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University of Southern California

2016 年 03 月 13 日 7:30 上午 - 2016 年 03 月 16 日 5:00 下午

Center for the Health Professionals, 1540 Alcazar Street #140, Los Angeles, CA 90089

Regulatory Affairs: The IND, NDA, and Postmarketing

Session 20: Post-NDA Approval Regulatory Requirements

Session Chair(s)

Michael  Hamrell, PHD, RAC

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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