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Business · 14/07/20091 min read

FDA Announces Guidance for IRB Registration

The Food and Drug Administration (FDA) has released a guidance document to help Institutional Review Boards (IRBs) comply with a new rule requiring registration with the Department of Health and Human Services (HHS) for reviewing FDA-regulated research in the United States.

Original source language: Federal Register — Food and Drug AdministrationOpen original release →

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