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FDA Issues Draft Guidance for Remote Evaluations of Drug Manufacturing and Bioresearch Monitoring Facilities

ComplianceLogix October 25, 2023

The U.S. Food and Drug Administration issued a guidance on voluntary remote interactive evaluations at facilities where drugs are manufactured, processed, packed, compounded, or held, and at drug facilities.

Read the full draft guidance here

Source: https://www.fda.gov/media/173286/download
In FDA, audit Tags FDA Guidance, FDA
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