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

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

523. S9 nonclinical evaluation for anticancer pharmaceuticals: questions and answers

524. Assessing user fees under the biosimilar user fee amendments of 2017

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

528. Use of electronic health record data in clinical investigations

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