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CMC Considerations for Biotechnology Product Development: A Regulatory Perspective

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U.S. Food and Drug Administration

FDA discusses regulatory expectations for biotechnology products, regulatory challenges, and strategies for success.
Presenters:
Wendy Weinberg, PhD, Chief, Laboratory of Molecular Oncology
Kristen Nickens, PhD, Product Quality Team Lead
Office of Biotechnology Products (OBP), Office of Pharmaceutical Quality (OPQ), CDER

Learn more at: https://www.fda.gov/drugs/newsevents...

FDA CDER’s Small Business and Industry Assistance (SBIA) educates and provides assistance in understanding the regulatory aspects of human drug products & clinical research.  
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Phone (301) 7966707 I (866) 4055367

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