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Guidance Documents/Guidance-Document/Master Protocols: Efficient Clinical Trial Design Strategies to Expedite Development of Oncology Drugs and Biologics Guidance for Industry: Guidance for Industry

Master Protocols: Efficient Clinical Trial Design Strategies to Expedite Development of Oncology Drugs and Biologics Guidance for Industry: Guidance for Industry

Detailed guidance document from FDA and regulatory agencies.

Document Details

Guidance Document

March 1, 2022

April 11, 2024

Center for Drug Evaluation and Research

102e00b9-5d33-4bc1-ac6f-2d1c86b63720

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