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505(b)(2) NDA or ANDA? (10of28) Generic Drugs Forum - Apr. 3-4, 2019 

U.S. Food and Drug Administration
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CDER Office of Generic Drugs’ Elizabeth Friedman and Office of New Drugs’ Beth Goldstein provide practical regulatory and scientific advice on selecting the appropriate abbreviated pathway for a proposed product.
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
LinkedIn: / cder-small-business-an...
Twitter: / fda_drug_info
CDER small business e-mail update subscription: updates.fda.gov/subscriptionm...

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7 авг 2024

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