A-Z Index

A

• Adverse Event Reporting
• Advertisements Guidelines (PDF)
• Amendments
• American Indian Research (PDF)

• Animals
• Assent Forms
• Assent Process
• Assessing Risk for Human Participants (PDF)

B

• Belmont Report
• Biosafety Hazard

• Biological Specimens
•  

C

• 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

• 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

• 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

• FDA Drug Trials (PDF)
• Federal Wide Assurance - FWA (HTML)
• Fee Schedule

• Fee FAQ (PDF)
• Fetal Research (PDF)

G

• General Clinical Research Center
• Genetic Research

H

• 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

• 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

K

L

M

• Medical Devices
• Model Tribal Research Code (PDF)
• Monitoring Research Data (DOC)

N

• New Board Member Handbook (PDF)
• Native American Research (PDF)

O

• Organ Transplant Research (PDF)

P

• 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

• Questionnaire Cover Letter

R

• 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

• Sensitive Research Subjects - Privacy and Confidentiality (PDF)
• Short Form Consent Instructions for Use (PDF)

• Sponsor - Investigator Guidelines and Responsibilities (PDF)
• Student Research

T

• Technology Commercialization Office
• Tissue / Specimen Banking
• Tracked Changes

• Transplantation of Fetal Tissue (PDF)
• Treatment Investigational Device Exemption

U

• Unanticipated Problems
• UUSHC Pharmacy Policies (DOC)

V

• 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
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W

• Waiver of Informed Consent
• Who May Submit a Study

• Writing a Review Summary

X

Y

Z