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A
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Adverse Event Reporting
Advertisements Guidelines (PDF)
Amendments
American Indian Research (PDF)
Animals
Applicable State Laws
Assent Forms
Assent Process
Assessing Risk for Human Participants (PDF)
B
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Belmont Report
Board Member Handbook
Biological Specimens
Biosafety Hazard
C
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Cancer Patients
Certificate of Confidentiality
Children in Research (PDF)
Close a Study
Code of Federal Regulations 21 CFR 56 (PDF)
Common Rule (45 CFR 46) (PDF)
Compassionate Use of Investigational Devices
Compensation
Consent Forms
Consent Process for Cognitively Impaired Adults (PDF)
Continued Access to Investigational Devices
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 - FDA Guidance
E
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Emergency Use of a Test Article
Engagement of Institutions in Research - OHRP Guidance
Event Reporting
Exempt Categories of Research (PDF)
Exercise Testing (PDF)
Expedited Review of Research (PDF)
External Institutions Policy
F
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Federal Wide Assurance - FWA (HTML)
Fee Schedule
Fee FAQ (PDF)
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General Clinical Research Center
Genetic Research
H
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HIPAA Privacy Rule & Authorization
HIPAA Privacy Rule - Databases and Research Repositories - NIH Guidance
HIPAA Privacy Rule Information for IRBs - NIH Guidance
HIPAA Privacy Rule Information for Researchers - NIH Guidance
HIV and Public Health Services (PHS) Research
HIV Antibody Testing
Humanitarian Use Devices
Human Tissue Transfer
I
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Institutional Review Boards - 21 CFR Part 56 (PDF)
Investigational Device Exemption (IDE)
Investigator Qualifications
Investigator Guidance Series
Investigator Responsibilities for Device Studies
Investigator Responsibilities for Drug Studies
IRB Registration
IRB Review Process
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Legally Authorized Representatives
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Material Transfer Agreements (MTA)
Medical Devices
Monitoring Research Data (DOC)
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New Board Member Handbook (PDF)
Native American Research (PDF)
Neonates in Research
O
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Observation of Consent
Organ Transplant Research (PDF)
P
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Parental Permission Process
Participant Selection for Research (PDF)
Payment Arrangements for Research Personnel
Placebo Guidelines (PDF)
Pregnant Women and Fetuses (PDF)
Preparation Packed Investigator-Initiated Drug and Device Studies
Prisoners (PDF)
Principal Investigator (PI) Responsibilities
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
Quality Improvement Activities FAQ - OHRP Guidance
R
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Radiation and X-Ray Use
Radioactive Materials and X-Rays (PDF)
Recruiting Materials (PDF)
Recruitment and Enrollment of Employees
Required Training (HTML)
Research Design (PDF)
Research Involving External Institutions (HTML)
Research Involving Students
Research, Vice President
Revising Documents
RGE Procedures for Contacting Individuals
Risk Assessment
S
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Secondary Data - Analysis of Existing Datasets
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
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)
VA Research Involving Cognitively Impaired Participants
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
Wards of State
Who May Submit a Study
Writing a Review Summary
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