FDA Biologics (BLA & Biosimilars)Original article
Good Clinical Practices Are Not Optional: The FDA’s Commitment to Human Subject Protections and Gold Standard Science in an Era of Global Clinical Research
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Summary
The FDA reaffirms its commitment to Good Clinical Practices (GCP) as a scientific and ethical foundation for regulatory decisions, emphasizing that GCP compliance is not optional bureaucratic formality but essential for human subject protections and quality science in global clinical research.
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regulatoryGCPcomplianceclinical researchhuman subject protections
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Published by FDA Biologics (BLA & Biosimilars) on September 3, 2026 3:40 PM
