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1421. Citizen petitions and petitions for stay of action subject to section 505(q) of the Federal Food, Drug, and Cosmetic Act

1422. Wholesale distributor verification requirement for saleable returned drug product: compliance policy

1423. Amyotrophic lateral sclerosis: developing drugs for treatment

1424. Changes to existing medical software policies resulting from section 3060 of the 21st Century Cures Act: guidance for industry and Food and Drug Administration staff

1425. Bacterial risk control strategies for blood collection establishments and transfusion services to enhance the safety and availability of platelets for transfusion

1426. Further testing of donations that are reactive on a licensed donor screening test for antibodies to hepatitis C virus

1427. Investigational enzyme replacement therapy products: nonclinical assessment

1428. Investigational in vitro diagnostics in oncology trials: streamlined submission process for study risk determination

1429. Prescription Drug User Fee Act waivers, reductions, and refunds for drug and biological products

1430. Process to request a review of FDA's decision not to issue certain export certificates for devices: guidance for industry and Food and Drug Administration staff