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Business · 07/06/2011

FDA Announces Guidance on Enforcement of Safety Reporting Requirements for INDs and BA/BE Studies

The FDA is providing a guidance document to inform industry and investigators about the agency's plan to exercise enforcement discretion regarding safety reporting requirements for Investigational New Drug Applications and Bioavailability/Bioequivalence Studies, with the goal of giving sponsors and investigators more time to comply with the regulations.

Original source language: Federal Register — Health and Human ServicesOpen original release →

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