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Announcement:
The federal administration has enacted a number of Executive Orders that have implications for federal proposals and awards.
View more information on research activity impacts.
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Information for IRB members
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Human Research
General IRB Info
Human Research Protection Policy Manual
Policy Manual Definitions
Browse the definitions of technical terms in the Policy Manual
For Researchers & Affiliates
International Research
Research in Schools (K-12)
University Student Participants
Veterans Affairs Research
Clinical Research Resources
Clinical Trials Project Life Cycle
Clinical Trials Study Management
Data Safety & Monitoring
Sample Data Safety & Monitoring Plan Outline
Clinical Trials Contract & Budget
Regulatory Resources
Clinical Trial Requirements
Clinical Trials Investigator-initiated Research
Clinical Trial Registration FAQs
HIPAA and Human Subjects Research
Obtaining Human Research Data Under HIPAA
Quality Assurance Review
Consent Process Aids
Revised Common Rule requirements for informed consent
Creating Recruitment Materials
(Current Page)
For IRB Members
Completing a First-rate Review
For Research Participants
¿Debo participar en un estudio científico?
Information for research participants translated in Spanish
Information for IRB members
General IRB information
IRB meeting schedule and information
IRB review fees
Levels of IRB review
General IRB information
IRB member resources
Completing a first-rate review: Your responsibilities as an IRB reviewer
