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1871. Drugs for treatment of partial onset seizures: full extrapolation of efficacy from adults to pediatric patients 2 years of age and older

1872. Humanitarian device exemption (HDE) program: guidance for industry and Food and Drug Administration staff

1874. Citizen petitions and petitions for stay of action subject to section 505(q) of the Federal Food, Drug, and Cosmetic Act

1875. Wholesale distributor verification requirement for saleable returned drug product: compliance policy

1876. Amyotrophic lateral sclerosis: developing drugs for treatment

1877. 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

1878. Bacterial risk control strategies for blood collection establishments and transfusion services to enhance the safety and availability of platelets for transfusion

1879. Further testing of donations that are reactive on a licensed donor screening test for antibodies to hepatitis C virus

1880. Investigational enzyme replacement therapy products: nonclinical assessment