U.S. Department of Health & Human Services

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81. Drug and device manufacturer communications with payors, formulary committees, and similar entities: questions and answers : guidance for industry and review staff


82. Logical observation identifiers names and codes for in vitro diagnostic tests: guidance for industry and Food and Drug Administration staff


86. Revised recommendations for reducing the risk of Zika virus transmission by blood and blood components


90. Clarification of orphan designation of drugs and biologics for pediatric subpopulations of common diseases


100. Classification of products as drugs and devices & additional product classification issues: final guidance : guidance for industry and FDA staff