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Business · 24/11/2014

FDA Issues Final Guidance for Human Drug Compounding Outsourcing Facilities Under Section 503B of the FD&C Act

The FDA has released a final guidance to help human drug compounders comply with new regulations, outlining the process for registering, re-registering, or de-registering outsourcing facilities with the agency

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

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