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33. Medicaid: further action needed to expedite use of national data for program oversight : report to Congressional requesters

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

39. Live case presentations during investigational device exemption (IDE) clinical trials: guidance for institutional review boards, industry, clinical investigators, and Food and Drug administration staff

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