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1. FDA should further integrate its review of cybersecurity into the premarket review process for medical devices

2. SCHIP at the crossroads: California's options in responding to new federal funding conditions

3. No free lunch?: current challenges facing National School Lunch and School Breakfast Programs

4. A randomized trial testing the effect of narrative vignettes versus guideline summaries on provider response to a professional organization clinical policy for safe opioid prescribing

22. A Statement

63. Antibiotics: FDA has encouraged development, but needs to clarify the role of draft guidance and develop qualified infectious disease product guidance : report to Congressional requesters

64. CT contrast media power injectors can rupture conventional IV sets

66. Multidrug-resistant organisms--strategies to reduce infection

67. Hazardous spills: the safe handling of hazardous drugs

73. The Debt to Taft

82. Medicare Advantage benefit design: what does it provide, what doesn't it provide, and should standards apply?

83. Standards development and the use of standards in regulatory submissions reviewed in the Center for Biologics Evaluation and Research

84. Use of International Standard ISO 10993-1, "Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process": guidance for industry and Food and Drug Administration staff

86. Surgical fires: trends associated with prevention efforts