Grant Administration Regulations
Regulations from several entities guide the management of your grant. If you have any questions about regulations and how they apply to your grant, contact your grantee organization.
- Ahrens, T. (2005). Evidenced-based practice: Priorities and implementation strategies. AACN Advanced Critical Care, 16(1), 36-42.
- Cook, D. (1998). Evidence-based critical care medicine: A potential tool for change. New Horizon, 6(1), 20-25.
- Kelley, P. (2002). Research to practice in the military health care system. TSNRP grant N02-P18.
- Nieva, V., Murphy, R., Ridley, N., Donaldson, N., Combers, J., Mitchell, P., et al. (2005). From science to service: A framework for the transfer of patient safety research into practice. In Advances in patient safety: From research to implementation (vol. 2, pp. 441-453). Rockville, MD: Agency for Healthcare Research and Quality.
- Sackett, K. L., Straus, S. E., Richardson, W. S., Rosenberg, W., & Haynes, R. B. (2000). Evidence-based medicine; How to practice and teach EBM. London: Churchill Livingstone.
- Titler, M. G. (2006). Developing and evidence-based practice (6th ed.). St Louis, MO: Mosby, Inc.
Grant Management Regulations
Human Subjects Protection
- DoD Instruction 1100.13, Surveys of DoD Personnel.
- DoD Directive 3216.02, Protection of Human Subjects and Adherence to Ethical Standards in DoD Supported Research.
- DoD Directive 6000.8, Funding and Administration of Clinical Investigation Programs.
- HA Policy 05-003, Policy for Protection of Human Subjects in DoD Sponsored Research, Health Affairs Under Secretary of Defense for Personnel and Readiness, 28 Mar 2005.
- Title 10 U.S. Code 980, Limitations on Use of Humans as Experimental Subjects.
- DoD Directive 6200.02, Application of Food and Drug Administration (FDA) Rules to Department of Defense Force Health Protection Programs.
- Title 21 Code of Federal Regulations (CFR) 50, Protection of Human Subjects.
- Title 21 Code of Federal Regulations (CFR) 56, Institutional Review Boards.
- Title 21 Code of Federal Regulations (CFR) 312, Investigational New Drug Application.
- Title 21 Code of Federal Regulations (CFR) 812, Food and Drugs Chapter I: Food and Drug Administration Department of Health and Human Services, Subchapter H: Medical Devices, Part 812. Investigational Device Exemptions.
- Title 21 Code of Federal Regulations (CFR) 600, Biological Products, General.
- Title 21 Code of Federal Regulations (CFR) 314, Applications for FDA Approval to Market a New Drug.
- Title 32 CFR 219, Human Subjects Protection.
- Title 45 CFR 46, Subparts A, B, C, and D, Protection of Human Subjects.
- Title 5 U.S. Code 5536, Extra Pay for Extra Services Prohibited.
- Title 24 U.S. Code 30, Payment to Donors of Blood for Persons Undergoing Treatment at Government Expense.
- Health Affairs Policy 97-033, Policy for External Peer Review for Defense Health Program Extramural Medical Research Involving Human Subjects.
U.S. Army Regulations
U. S. Navy Regulations
U.S. Air Force Regulations
Non-Human Animal Subjects
- NIH, Office of Laboratory Animal Welfare.
- DoD Directive 3216.1, The Use of Animals in DoD Programs.
- Title Code of Federal Regulations (CFR) Subpart A-D, Animals and Animal Products.
- Public Law 99-158, Animals in Research, November 20, 1985.
- International Guiding Principles for Biomedical Research Involving Animals (1985), Council for International Organizations of Medical Sciences (CIOMS).
- American Veterinary Medical Association (AVMA), AVMA Guidelines on Euthanasia, June 2007.
- USUHSINST 3203, The Care and Use of Laboratory Animals in DoD Programs, incorporates Army Regulation 40-33, SECNAVINST 3900.38, AFMAN 40-401(1), and DARPAINST 18 (Defense Advanced Research Projects Agency Instruction).
Public Affairs Policies and Procedures