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591. Duchenne muscular dystrophy and related dystrophinopathies: developing drugs for treatment

592. How to prepare a pre-request for designation (pre-RFD)

594. Q11 development and manufacture of drug substances (chemical entities and biotechnological/biological entities): questions and answers

595. E6(R2) good clinical practice: integrated addendum to ICH E6(R1)

596. M7(R1) assessment and control of DNA reactive (mutagenic) impurities in pharmaceuticals to limit potential carcinogenic risk

597. E18 genomic sampling and management of genomic data

598. Chronic obstructive pulmonary disease: use of the St. George's Respiratory Questionnaire as a PRO assessment tool

599. Liposome drug products: chemistry, manufacturing, and controls : human pharmacokinetics and bioavailability : and labeling documentation

600. E11(R1) addendum: clinical investigation of medicinal products in the pediatric population