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Guidance Documents/Guidance-Document/Hematologic Malignancies: Regulatory Considerations for Use of Minimal Residual Disease in Development of Drug and Biological Products for Treatment: Guidance for Industry

Hematologic Malignancies: Regulatory Considerations for Use of Minimal Residual Disease in Development of Drug and Biological Products for Treatment: Guidance for Industry

Detailed guidance document from FDA and regulatory agencies.

Document Details

Guidance Document

January 24, 2020

January 24, 2020

Center for Drug Evaluation and Research

5e0485fc-a570-4965-bae5-05741639f886

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