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262. Intent to exempt certain unclassified medical devices from premarket notification requirements: guidance for industry and Food and Drug Administration staff

265. Opioid use disorder: developing depot buprenorphine products for treatment

266. Evaluation of devices used with regenerative medicine advanced therapies

267. Considerations for the inclusion of adolescent patients in adult oncology clinical trials

268. Severely debilitating or life-threatening hematologic disorders: nonclinical development of pharmaceuticals

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

270. Medical devices containing materials derived from animal sources (except for in vitro diagnostic devices): guidance for industry and Food and Drug Administration staff