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Alphabetical List of IRB Guidance Documents

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A Pediatric Research “Assent Matrix”
Alabama Law on Children, Minors, Consent, and Other Research-Related Topics
Copyrighted Instruments and IRB Applications

Department of Defense Regulations for Human Subjects Research
(updated 7-28-14)
Department of Energy Regulations for Human Subjects Research
Developing a Data and Safety Monitoring Plan (DSMP) or a Data Safety Monitoring Board (DSMB)
Environmental Protection Agency Requirements for Human Subjects Research
Evaluating Sound Study Design

Examples of Assent Forms
Family Educational Rights and Privacy Act (FERPA)
General Responsibilities of Investigators
Information on Oral History Projects
Informed Consent
International Research

IRB Advertising Guidelines
IRB Application Guide
IRB Determinations and Motions

Investigators and Legally Authorized Representatives
Legislation on School-Based Surveys and Passive Consent: No Child Left Behind (Public Law 107-110)
Mandatory Reporting Laws Affecting Research Conducted in Alabama
Meaning of Departmental Signature on Signature Assurance Sheet
Minor Changes to Approved Protocols
Model Telephone Consent
Protection of Human Subjects in HIV/AIDS-Related Research
Public Datasets Approved for Secondary Analysis Without IRB Review
Regulatory Requirements for Investigators Who Hold INDs or IDEs
Reportable Events
Research and You: Know Your Rights (English and Spanish)
Sample Consent for a Medical/Health-Related Study
Sample Consent for Non-Medical Study
Student Researchers at UA
Student Research Participants
Template: Informed Consent for Medical/Health-Related Study
Template: Informed Consent for Non-Medical Study
Template for Study Presentation for Web Surveys
The Meaning of Anonymous, Confidential, and De-Identified and Implications for Data Sharing or Re-Use
Use of Deception/Concealment in Research
Writing Understandable Consent Forms

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