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

72. Maximal usage trials for topically applied active ingredients being considered for inclusion in an over-the -counter monograph: study elements and considerations

73. Considerations in demonstrating interchangeability with a reference product

74. Premarket tobacco product applications for electronic nicotine delivery systems

76. Delayed graft function in kidney transplantation: developing drugs for prevention

77. Live case presentations during investigational device exemption (IDE) clinical trials: guidance for institutional review boards, industry, clinical investigators, and Food and Drug administration staff

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