he recently issued FDA guidance mandates manufacturers, packers, and distributors to adhere to new standards, emphasizing mandatory product and facility registrations, creation of safety substantiation information, and implementation of adverse event reporting. Daron breaks down key definitions, clarifies information submission processes, and discusses public accessibility. 

Tune in to stay informed about the crucial expectations, including adverse event reporting, recordkeeping, and safety substantiation, to ensure compliance with the evolving regulatory landscape.

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