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Quick Read FDA s New Draft Guidance On Data Integrity For In Vivo BABE Studies
The FDA has released a draft guidance, Data Integrity for In Vivo Bioavailability and Bioequivalence Studies. This article shares a concise summary.
Susan shockey
Us food drug administration
Human services
Us food drug administration
Department of health
Data integrity
Vivo bioavailability
Bioequivalence studies
Quality control
For public comments by june
Draft guidance
Integrating data integrity
Why invest
Quality management system
Clarkston consulting
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