REdI Annual Conference 2024: CBER (Biologics) Innovation in Medical Product Development (Day 2 of 2)

Поделиться
HTML-код
  • Опубликовано: 29 май 2024
  • Learn directly from the FDA’s regulatory experts in medical product centers: drugs, devices, and biologics. This course is designed to provide participants with a strong, basic foundation in the FDA’s regulatory requirements, and also create awareness of current activities.
    6:07 CBER Track Day 2 Welcome - Larissa Lapteva, MD, MHS, MBA
    12:52 Session 1: Introduction of Hector S. Izurieta, MD, MPH, PhD
    14:26 Use of Real-World Evidence in Accelerated Approval - Hector S. Izurieta, MD, MPH, PhD
    32:56 Session 1: Introduction of Peter J. Weina, PhD, MD
    34:36 Artificial Intelligence Challenges for Regulating Vaccine Development - Peter J. Weina, PhD, MD
    57:01 Session 1: Introduction of Sudhakar Agnihothram, BPharm, PhD
    58:14 CBER’s Advanced Manufacturing Programs for Sponsors - Sudhakar Agnihothram, BPharm, PhD
    1:27:19 Q&A with Session 4 Speakers
    2:04:58 Introduction of Session 5 - Larissa Lapteva, MD, MHS, MBA
    2:05:55 Session 5: Introduction of Meghna Alimchandani, MD
    2:07:02 Postmarketing Surveillance for Product Safety in Pregnancy - Meghna Alimchandani, MD
    2:45:47 Session 5: Introduction of Craig Zinderman, MD, MPH
    2:47:11 Update on the ICH E2D(R1) Guideline: Post-Approval Safety Data: Definitions and Standards for Management and Reporting of Individual Case Safety Reports (ICSRs) - Craig Zinderman, MD, MPH
    3:23:57 Q&A with Session 5 Speakers
    4:34:35 Introduction of Session 6 - Melek Sunay, PhD
    4:35:04 Session 6: Introduction of Orieji Illoh, MD
    4:36:10 Blood Regulation and Safety - Orieji Illoh, MD
    5:07:52 Session 6: Introduction of Julia Tait Lathrop, PhD
    5:09:03 FDA Regulation of HIV Tests - Julia Tait Lathrop, PhD
    5:43:51 Q&A with Session 6 Speakers
    6:19:35 Introduction of Session 7 - Larissa Lapteva, MD, MHS, MBA
    6:20:13 Session 7: Introduction of Triet M. Tran, PharmD, BCSCP
    6:21:19 The Center for Biologics Evaluation and Research (CBER) Bioresearch Monitoring Program - Triet M. Tran, PharmD, BCSCP
    6:53:36 Session 7: Introduction of Seth Schulte, MS
    6:54:37 CBER’s Perspective on Evaluation and Implementation of Rapid Microbial Methods - Seth Schulte, MS
    7:26:43 Q&A with Session 7 Speakers
    7:37:56 CBER Track Closing Remarks

Комментарии •