Components of New Drug Application and Biologics License Application (5of15) REdI- May 29-30, 2019

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  • เผยแพร่เมื่อ 21 พ.ค. 2024
  • Swati Patwardhan from CDER’s Office of New Drugs discusses review application approval pathways. She covers content and format of an application, review forms, and documentation with examples on best practices related to module I.
    Learn more at www.fda.gov/drugs/cder-small-...
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    FDA CDER’s Small Business and Industry Assistance (SBIA) educates and provides assistance in understanding the regulatory aspects of human drug products & clinical research.
    Visit www.fda.gov/cdersbia and www.fda.gov/cdersbialearn for news and a repository of training activities.
    Email: CDERSBIA@fda.hhs.gov
    Phone: (301) 796-6707 I (866) 405-5367
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    CDER small business e-mail update subscription: updates.fda.gov/subscriptionm...
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