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Start Over You searched for: Subjects United States. Department of Health and Human Services. Remove constraint Subjects: United States. Department of Health and Human Services. Languages English Remove constraint Languages: English Publication Year 2017 Remove constraint Publication Year: <span class="single" data-blrl-single="2017">2017</span>

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

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

93. 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

94. 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

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

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

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

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

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