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

594. Clinical trial imaging endpoint process standards

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

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

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

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

600. Bioanalytical method validation