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Start Over You searched for: Subjects United States. Food and Drug Administration. Remove constraint Subjects: United States. Food and Drug Administration. Publication Year 2017 to 2019 Remove constraint Publication Year: <span class="from" data-blrl-begin="2017">2017</span> to <span class="to" data-blrl-end="2019">2019</span>

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21. Use of public human genetic variant databases to support clinical validity for genetic and genomic-based in vitro diagnostics: guidance for stakeholders and Food and Drug Administration staff

23. Q7 good manufacturing practice guidance for active pharmaceutical ingredients: questions and answers

25. Clinical trial imaging endpoint process standards

26. Assessing user fees under the Prescription Drug User Fee Amendments of 2017

27. S3A guidance: note for guidance on toxicokinetics : the assessment of systemic exposure in toxicity studies : focus on microsampling : questions and answers

29. Establishing effectiveness for drugs intended to treat male hypogonadotropic hypogonadism attributed to nonstructural disorders

30. Acne vulgaris: establishing effectiveness of drugs intended for treatment