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8481. Humanitarian device exemption (HDE) program: guidance for industry and Food and Drug Administration staff

8483. Citizen petitions and petitions for stay of action subject to section 505(q) of the Federal Food, Drug, and Cosmetic Act

8484. Wholesale distributor verification requirement for saleable returned drug product: compliance policy

8485. Amyotrophic lateral sclerosis: developing drugs for treatment

8486. 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

8487. Bacterial risk control strategies for blood collection establishments and transfusion services to enhance the safety and availability of platelets for transfusion

8488. Further testing of donations that are reactive on a licensed donor screening test for antibodies to hepatitis C virus

8489. Investigational enzyme replacement therapy products: nonclinical assessment

8490. Investigational in vitro diagnostics in oncology trials: streamlined submission process for study risk determination