NATIONAL INSTITUTES OF HEALTH
Site Map
- Sheet 1
- Responsibilities of the Office of Human Subjects Research
- Sheet 2
- Institutional Review Board Leadership
- Sheet 3
- Criteria for Institutional Review Board (IRB) Approval of Research Involving Human Subjects
- Sheet 4
- Deleted
- Sheet 5
- Guidelines for Writing Research Protocols
- Sheet 6
- Guidelines for Writing Informed Consent Documents
- Sheet 7
- Research Involving Cognitively Impaired Subjects: A Review of Some Ethical Considerations
- Sheet 8
- Answers to Questions Frequently asked of NIH's Office of Human Subjects Research (OHSR)
- Sheet 9
- Continuing Review of Research Involving Human Subjects
- Sheet 10
- Research Involving Children
- Sheet 11
- Inclusion of Women and Minorities in Study PopulationsGuidance for IRBs and Principal Investigators
- Sheet 12
- NIH Institutional Review Board Administrative Procedures
- Sheet 13
- Issues Regarding Blinded, Randomized Studies in the NIH Intramural Research Program
- Sheet 14
- NIH Requirements for the Research Use of Stored Human Specimens and Data | DDIR memorandum
- Sheet 15
- Points to Consider in Development of Informed Consent Documents that Include the Collection and Research Use of Human Biological Materials.
This sheet is currently under Revision.
- Sheet 16
- NIH Institutional Review Board (IRB) Minutes
- Sheet 17
- Procurement and Use of Human Biological Materials For Research
- Sheet 18
- Guidelines for NIH Intramural Investigators and Institutional Review Boards on Data and Safety Monitoring
- Sheet 19
- Criteria for Selection and Use of Alternate Members on NIH Institutional Review Boards
- Sheet 20
- Remuneration of Research Subjects in the Intramural Research Program
- Form 1
- Request For Review Of Research Activity Involving Human Subjects (“Exempt”Form) - .doc format
- Form 2
- Format for IRB Minutes
