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

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

13. 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

14. 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

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

18. Clinical trial imaging endpoint process standards

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

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