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Business · 13/01/2017

FDA Issues Final Guidance on Repackaging of Human Drug Products by Pharmacies and Outsourcing Facilities

The FDA has released a final guidance outlining the conditions under which it will not take enforcement action for certain violations of the FD&C Act when pharmacies or outsourcing facilities repack certain human drugs.

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

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