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8382. Intent to exempt certain unclassified medical devices from premarket notification requirements: guidance for industry and Food and Drug Administration staff

8385. Opioid use disorder: developing depot buprenorphine products for treatment

8386. Evaluation of devices used with regenerative medicine advanced therapies

8387. Considerations for the inclusion of adolescent patients in adult oncology clinical trials

8388. Severely debilitating or life-threatening hematologic disorders: nonclinical development of pharmaceuticals

8389. Enrichment strategies for clinical trials to support determination of effectiveness of human drugs and biological products

8390. Medical devices containing materials derived from animal sources (except for in vitro diagnostic devices): guidance for industry and Food and Drug Administration staff