Clinical Pharmacology Considerations for Radiolabeled Mass Balance Studies

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  • เผยแพร่เมื่อ 28 พ.ย. 2024
  • This webinar discussed the final guidance for the industry Clinical Pharmacology Considerations for Human Radiolabeled Mass Balance Studies which was published in July 2024. FDA subject matter experts addressed recommendations from the guidance including, deciding whether and when to conduct the study, as well as how to design and report results from a human radiolabeled mass balance study.
    Timestamps
    06:58 - Background and Overview
    13:20 - Considerations for Designing Mass Balance Studies and Reporting
    23:58 - Q&A Discussion Panel
    Speakers | Panelists:
    Anuradha Ramamoorthy, Ph.D. FCP
    Master Scientist & Policy Lead
    Guidance & Policy Team
    Office of Clinical Pharmacology (OCP)
    Office of Translational Sciences (OTS) | CDER | FDA
    Zhixia (Grace) Yan Danielsen, Ph.D.
    Deputy Director
    Division of Infectious Disease Pharmacology
    OCP | OTS | CDER | FDA
    Suresh Doddapaneni, Ph.D.
    Deputy Director
    Division of Inflammation and Immune Pharmacology
    OCP | OTS | CDER | FDA
    Learn more at: www.fda.gov/dr...
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