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

292. Pediatric information for x-ray imaging device premarket notifications: guidance for industry and Food and Drug Administration staff

293. Nucleic acid testing (NAT) for human immunodeficiency virus type 1 (HIV-1) and hepatitis C virus (HCV): testing, product disposition, and donor deferral and reentry

294. FDA categorization of investigational device exemption (IDE) devices to assist the Centers for Medicare and Medicaid Services (CMS) with coverage decisions: guidance for sponsors, clinical investigators, industry, institutional review boards, and Food and Drug Administration staff

295. Technical considerations for additive manufactured medical devices: guidance for industry and Food and Drug Administration staff

296. Use of serological tests to reduce the risk of transmission of Trypanosoma cruzi infection in blood and blood components

297. Software as a medical device (SAMD): clinical evaluation : guidance for industry and Food and Drug Administration staff

299. Systemic antibacterial and antifungal drugs: susceptibility test interpretive criteria labeling for NDAs and ANDAs

300. Waiver of in vivo bioavailability and bioequivalence studies for immediate-release solid oral dosage forms based on a biopharmaceutics classification system