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1881. Investigational in vitro diagnostics in oncology trials: streamlined submission process for study risk determination

1882. Prescription Drug User Fee Act waivers, reductions, and refunds for drug and biological products

1883. 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

1884. Smallpox (variola virus) infection: developing drugs for treatment or prevention

1885. Compliance policy for limited modifications to certain marketed tobacco products

1886. Adaptive designs for clinical trials of drugs and biologics

1887. Considerations for the development of dried plasma products intended for transfusion

1888. Food labeling: serving sizes of foods that can reasonably be consumed at one eating occasion, reference amounts customarily consumed, serving size-related issues, dual-column labeling, and miscellaneous topics

1889. Enforcement priorities for electronic nicotine delivery systems (ENDS) and other deemed products on the market without premarket authorization

1890. VA health IT modernization: historical perspective on prior contracts and update on plans for new initiative : report to the House Committee on Oversight and Government Reform, Subcommittee on Information Technology