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1821. Evaluation of devices used with regenerative medicine advanced therapies

1822. Considerations for the inclusion of adolescent patients in adult oncology clinical trials

1823. Severely debilitating or life-threatening hematologic disorders: nonclinical development of pharmaceuticals

1824. Enrichment strategies for clinical trials to support determination of effectiveness of human drugs and biological products

1825. Medical devices containing materials derived from animal sources (except for in vitro diagnostic devices): guidance for industry and Food and Drug Administration staff

1826. Pediatric HIV infection: drug product development for treatment

1827. Human immunodeficiency virus-1 infection: developing systemic drug products for pre-exposure prophylaxis

1828. Interpretation of and compliance policy for certain label requirement: applicability of certain Federal Food, Drug, and Cosmetic Act requirements to vape shops

1829. Standards development and the use of standards in regulatory submissions reviewed in the Center for Biologics Evaluation and Research

1830. Pediatric information incorporated into human prescription drug and biological product labeling