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

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

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

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

106. E18 genomic sampling and management of genomic data

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

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

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

110. Considerations for design, development, and analytical validation of next generation sequencing (NGS)--based in vitro diagnostics (IVDs) intended to aid in the diagnosis of suspected germline diseases: guidance for stakeholders and Food and Drug Administration staff