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31. Osteoporosis: nonclinical evaluation of drugs intended for treatment

32. Placebos and blinding in randomized controlled cancer clinical trials for drug and biological products

33. Adaptive designs for clinical trials of drugs and biologics

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

36. Considerations for the use of real-world data and real-world evidence to support regulatory decision-making for drug and biological products: guidance for industry