A-Z Index

Please see the Glossary of Terms for additional explanations.

A	Back to Top
Adverse Events Flowchart 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) Audio Recordings Authorization (HIPAA)
B	Back to Top
Belmont Report Board Member Manual Biological Specimens	Biosafety Hazard Birth Control Breaches of Confidentiality
C	Back to Top
Cancer Patients Case Report Using Existing Data Author Worksheet Certificate of Confidentiality Checklist, Data and Safety Monitoring 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 Contraceptive Methods Covered Entity
D	Back to Top
Data and Safety Monitoring Board (DSMB) Guidelines (PDF) Data and Safety Monitoring - Ongoing (DOC) Data and Safety Monitoring Plan Checklist Data Safety Monitoring NIH Policy (DOC) Data Monitoring Using Self-Assessments	Deception in Social/Behavioral Science Research Declaration of Helsinki Device Research Device Studies, Investigator Responsibilities Drug Evaluation and Research - FDA Guidance Drug Studies, Investigator Responsibilities
E	Back to Top
Emergency Use of a Test Article Engagement of Institutions in Research - OHRP Guidance Employees in Research Equitable Selection of Participants Event Reporting	Exempt Categories of Research (PDF) Exempt Research Exercise Testing (PDF) Expedited Category 9 Expedited Review of Research (PDF) External Institutions Policy
F	Back to Top
Federal Wide Assurance - FWA (HTML) Fee Schedule	Fee FAQ (PDF)
G	Back to Top
General Clinical Research Center Genetic Research	Guidance for Accessing Protected Health Informaiton - UUHSC
H	Back to Top
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	Back to Top
Institutional Review Boards - 21 CFR Part 56 (PDF) Investigational Device Exemption (IDE) Investigator Guidance Series Investigational Pharmacy Policies Investigator Qualifications	Investigator Responsibilities for Device Studies Investigator Responsibilities for Drug Studies IRB Registration IRB Review Process
J	Back to Top

K	Back to Top

L	Back to Top
Legally Authorized Representatives Limited Data Set
M	Back to Top
Material Transfer Agreements (MTA) Medical Devices	Monitoring Research Data (DOC) Multimedia Recordings
N	Back to Top
New Board Member Manual (PDF) Native American Research (PDF)	Neonates in Research
O	Back to Top
Observation of Consent Organ Transplant Research (PDF)
P	Back to Top
Parental Permission Process Participant Resources Participant Selection for Research (PDF) Payment Arrangements for Research Personnel Pharmacy Policy Photographs for Research Purposes Placebo Guidelines (PDF) Pregnant Women and Fetuses (PDF) Pregnancy During Research Pregnant Partner	Preparation Packet 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) Privacy Rule (HIPAA) Protection of Human Subjects - 21 CFR 50 (PDF) Protocol Deviation Reporting (PDF)
Q	Back to Top
Questionnaire Cover Letter Quality Improvement Activities FAQ - OHRP Guidance
R	Back to Top
Radiation and X-Ray Use Recruitment Methods (PDF) Recruitment and Enrollment of Employees Reimbursement Required Training (HTML) Research Design (PDF) Research Involving External Institutions (HTML)	Research Involving Students Research Participant Resources Research Sites Outside the Covered Entity Research, Vice President Revising Documents RGE Procedures for Contacting Individuals Risk Assessment
S	Back to Top
Safe Harbor Safety Monitoring Secondary Data - Analysis of Existing Datasets Self-assessments Self Auditing a Study Short Form Consent Instructions for Use (PDF)	Sites Sponsor - Investigator Guidelines and Responsibilities (PDF) Statistical Analysis De-Identification Student Research Study Coordinator Toolkit
T	Back to Top
Technology Commercialization Office Tissue / Specimen Banking Tracked Changes	Transplantation of Fetal Tissue (PDF) Treatment Investigational Device Exemption
U	Back to Top
Unanticipated Problems UUHSC Pharmacy Policies (DOC)
V	Back to Top
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 Video Recordings Vulnerable Participants Veteran's Administration Salt Lake City Health Care System
W	Back to Top
Waiver of Informed Consent Wards of State	Who May Submit a Study Writing a Review Summary
X	Back to Top

Y	Back to Top

Z	Back to Top