FDA Regulatory Education for Industry (REdI) – Devices and Biologics Track
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FDA Regulatory Education for Industry (REdI) – Devices and Biologics Track
Presenters in the devices track discuss the following topics: Medical Device Single Audit Program (MDSAP), Public MAUDE Database, Additive Manufacturing, and FDA Review of Class I and II Recalls. Presenters during the biologics track discuss the following topics: Office of Tissues and Advanced Therapies (OTAT), 21 CFR Part 1271 "Tissue Rule ...
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