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12. Enrichment strategies for clinical trials to support determination of effectiveness of human drugs and biological products

13. Hematologic malignancies: regulatory considerations for use of minimal residual disease in development of drug and biological products for treatment

15. Investigational in vitro diagnostics in oncology trials: streamlined submission process for study risk determination

16. Adaptive designs for clinical trials of drugs and biologics

17. Institutional review board (IRB) review of individual patient expanded access submissions for investigational drugs and biological products: guidance for IRBs and clinical investigators