CDER is making available the webinar "What’s New with Forms FDA 3542a and 3542?" which provides an overview of the changes to Forms FDA 3542a and 3542 and walk through Form FDA 3542 using mock data.
CDR Kendra Stewart, R.Ph., Pharm.D.
Supervisor, Orange Book Team
Division of Legal and Regulatory Support (DLRS)
Office of Generic Drug Policy /Office of Generic Drugs (OGD)
Center for Drug Evaluation and Research (CDER)
U.S. Food and Drug Administration (FDA)
For questions concerning the webinar, please contact CDER SBIA at:
(866)-405-5367 | (301)-796-6707
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