Business · 05/12/2016Updated: 10/17/2026 · 1 min read

FDA Releases Guidance on Clinical Pharmacology Section of Labeling for Human Prescription Drugs

Summary

The FDA has finalized a guidance document to help pharmaceutical companies comply with regulations on labeling for human prescription drugs and biological products, outlining recommended information for the CLINICAL PHARMACOLOGY section.

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

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