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1371. Enrichment strategies for clinical trials to support determination of effectiveness of human drugs and biological products

1372. Medical devices containing materials derived from animal sources (except for in vitro diagnostic devices): guidance for industry and Food and Drug Administration staff

1373. Pediatric HIV infection: drug product development for treatment

1374. Human immunodeficiency virus-1 infection: developing systemic drug products for pre-exposure prophylaxis

1375. Interpretation of and compliance policy for certain label requirement: applicability of certain Federal Food, Drug, and Cosmetic Act requirements to vape shops

1376. Standards development and the use of standards in regulatory submissions reviewed in the Center for Biologics Evaluation and Research

1377. Pediatric information incorporated into human prescription drug and biological product labeling

1378. Recommended content and format of non-clinical bench performance testing information in premarket submissions: guidance for industry and Food and Drug Administration staff

1379. Hematologic malignancies: regulatory considerations for use of minimal residual disease in development of drug and biological products for treatment

1380. REMS: FDA's application of statutory factors in determining when a REMS is necessary