Stefan Lehnardt’s Post

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IP Associate at Foley & Lardner

In April 2024, the FDA published draft guidance on data integrity for in vivo bioavailability and bioequivalence studies. This article addresses what you need to know to keep track of your data. #technology #data

Keeping Track of Your Data — What You Need to Know about FDA’s Draft Guidance on Data Integrity for In Vivo Bioavailability and Bioequivalence Studies | Foley & Lardner LLP

Keeping Track of Your Data — What You Need to Know about FDA’s Draft Guidance on Data Integrity for In Vivo Bioavailability and Bioequivalence Studies | Foley & Lardner LLP

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