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31. Requests for feedback on medical device submissions: the pre-submission program and meetings with Food and Drug Administration staff : guidance for industry and Food and Drug Administration staff

32. General principles for evaluating the abuse deterrence of generic solid oral opioid drug products

34. Meta-analysis of federally funded teen pregnancy prevention programs: technical supplement

35. Meta-analysis of federally funded teen pregnancy prevention programs: final report

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

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

40. Considerations in demonstrating interchangeability with a reference product