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5022. Q7 good manufacturing practice guidance for active pharmaceutical ingredients: questions and answers

5023. Special protocol assessment

5024. Clinical trial imaging endpoint process standards

5025. Assessing user fees under the Prescription Drug User Fee Amendments of 2017

5026. S3A guidance: note for guidance on toxicokinetics : the assessment of systemic exposure in toxicity studies : focus on microsampling : questions and answers

5028. Establishing effectiveness for drugs intended to treat male hypogonadotropic hypogonadism attributed to nonstructural disorders

5029. Acne vulgaris: establishing effectiveness of drugs intended for treatment

5030. Bioanalytical method validation