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31. Considerations for building federal data capacity for patient-centered outcomes research related to intellectual and developmental disabilities

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

33. Considerations in demonstrating interchangeability with a reference product

35. Delayed graft function in kidney transplantation: developing drugs for prevention

39. Osteoporosis: nonclinical evaluation of drugs intended for treatment

40. Consideration of uncertainty in making benefit-risk determinations in medical device premarket approvals, de novo classifications, and humanitarian device exemptions: guidance for industry and Food and Drug Administration staff