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A
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Adverse Event Reporting
Advertisements Guidelines (PDF)
Amendments
American Indian Research (PDF)
Animals
Assent Forms
Assent Process
Assessing Risk for Human Participants (PDF)
B
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Belmont Report
Biosafety Hazard
Biological Specimens
C
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Cancer Patients
Certificate of Confidentiality
Children and Minors in Research (PDF)
Close a Study
Code of Federal Regulations 21 CFR 56 (PDF)
Coercion in the Consent Process (PDF)
Cognitively Impaired Researched Participants (PDF)
Common Rule (45 CFR 46) (PDF)
Compassionate Use
Compensation
Consent Forms
Consent Process (PDF)
Consent Process for Cognitively Impaired Adults (PDF)
Continued Access
Continuing Review - OHRP Guidance
Contraception (PDF)
Covered Entity
D
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Data and Safety Monitoring Board (DSMB) Guidelines (PDF)
Data and Safety Monitoring - Ongoing (DOC)
Data Safety Monitoring NIH Policy (DOC)
Deception in Social / Behavioral Science Research
Declaration of Helsinki
Device Research
Drug Evaluation and Research
E
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Emergency Use of a Test Article
Engagement of Institutions in Research
Event Reporting
Exempt Categories of Research (PDF)
Exercise Testing (PDF)
Expedited Review of Research (PDF)
External Institutions Policy
F
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FDA Drug Trials (PDF)
Federal Wide Assurance - FWA (HTML)
Fee Schedule
Fee FAQ (PDF)
Fetal Research (PDF)
G
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General Clinical Research Center
Genetic Research
H
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HIPAA - "Safe Harbor" Identifiers (PDF)
HIPAA Privacy Rule Information for IRBs
HIPAA Privacy Rule Information for Researchers
HIPAA Privacy Rule - Databases and Research Repositories
HIV and Public Health Services (PHS) Research
HIV Antibody Testing
Humanitarian Use Devices
I
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Institutional Review Boards - 21 CFR Part 56 (PDF)
Investigational Device Exemption (IDE)
Investigator Qualifications
Investigator Responsibility for Device Studies (PDF)
Investigator Responsibility for Drug Studies (PDF)
IRB Review Process
J
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M
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Medical Devices
Model Tribal Research Code (PDF)
Monitoring Research Data (DOC)
N
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New Board Member Handbook (PDF)
Native American Research (PDF)
O
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Organ Transplant Research (PDF)
P
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Participant Selection for Research (PDF)
Placebo Guidelines (PDF)
Pregnant Women and Fetuses (PDF)
Principal Investigator Qualifications (PDF)
Prisoners (PDF)
Prisoners: OHRP Guidance on the Involvement of Prisoners in Research (PDF)
Privacy and Confidentiality for Research Participants (PDF)
Protection of Human Subjects - 21 CFR 50 (PDF)
Protocol Deviation Reporting (PDF)
Q
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Questionnaire Cover Letter
R
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Radiation (HTML)
Radioactive Materials and X-Rays (PDF)
Recruiting Materials (PDF)
Required Training (HTML)
Research Design (PDF)
Research Involving External Institutions (HTML)
Research, Vice President
Revising Documents
Risk Assessment
S
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Sensitive Research Subjects - Privacy and Confidentiality (PDF)
Short Form Consent Instructions for Use (PDF)
Sponsor - Investigator Guidelines and Responsibilities (PDF)
Student Research
T
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Technology Commercialization Office
Tissue / Specimen Banking
Tracked Changes
Transplantation of Fetal Tissue (PDF)
Treatment Investigational Device Exemption
U
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Unanticipated Problems
UUSHC Pharmacy Policies (DOC)
V
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VA Consent Form (DOC)
VA Investigator Handbook (PDF)
VA Privacy Requirements for Disclosures for Research to Non-VA Researchers
VA Researcher Contact with Veterans: Cyber Security Memo 7.10.2006 (PDF)
VHA Data Use Requirements (PDF)
Vice President for Research
Vulnerable Participants
Veteran's Administration Salt Lake City Health Care System
W
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Waiver of Informed Consent
Who May Submit a Study
Writing a Review Summary
X
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Z
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