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17. Report of the Commission appointed by the Sanitary Board of the City Councils, to visit Canada for the investigation of the epidemic cholera, prevailing in Montreal and Quebec

40. Reports on epidemic cholera

44. Letters on yellow fever, the cholera, and quarantine: addressed to the Legislature of the state of New York, with an appendix containing correlative correspondence, and an act of the Legislature of the state, relative to the public health,with suggested amendments

55. Report

60. Report on the cholera in Paris

62. Report to enquire into the sufficiency of the legal provisions for the maintenance of untried prisoners and debtors: and report alterations and amendments with respect to the regulations affecting their condition. Mr. Gibbon, chairman

71. Rebalancing long-term care: the role of the Medicaid HCBS waiver program

73. Medicare and mental health: the fundamentals

74. Value-based coverage policy in the United States and the United Kingdom: different paths to a common goal

75. Health care price transparency and price competition

77. The prescription drug safety net: access to pharmaceuticals for the uninsured

81. Shaping Medicaid and SCHIP through waivers: the fundamentals

82. The Ryan White HIV/AIDS Program: the basics

86. The Medicare drug benefit coverage gap: the basics

87. National spending for long-term services and supports (LTSS): the basics

89. Classification of products as drugs and devices & additional product classification issues: final guidance : guidance for industry and FDA staff

90. Advancement of emerging technology applications for pharmaceutical innovation and modernization

91. Compliance policy for required warning statements on small-packaged cigars

92. Center for Devices and Radiological Health appeals processes: questions and answers about 517A : guidance for industry and Food and Drug Administration staff

93. Developing and responding to deficiencies in accordance with the least burdensome provisions: guidance for industry and Food and Drug Administration staff

94. Requests for feedback on medical device submissions: the pre-submission program and meetings with Food and Drug Administration staff : guidance for industry and Food and Drug Administration staff

95. Administrative procedures for CLIA categorization: guidance for industry and Food and Drug Administration staff

96. Display devices for diagnostic radiology: guidance for industry and Food and Drug Administration staff

97. M4 organization of the Common Technical Document for the Registration of Pharmaceuticals for Human Use

99. Deciding when to submit a 510(k) for a change to an existing device: guidance for Industry and Food and Drug Administration staff

100. Deciding when to submit a 510(k) for a software change to an existing device: guidance for industry and Food and Drug Administration staff