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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
Menu
Program Areas
Human Research
General IRB Info
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
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
Institutional Animal Care and Use Committee
Institutional Biosafety Committee
Responsible Conduct of Research
Research Misconduct
Research Security
U.S. Export Controls
Overview of Regulations
Policies and Procedures
Research Compliance
International Shipping
Foreign Workers and Visitors
Restricted Party Screening
Licensing
Recordkeeping Requirements
Reporting Violations
Protecting Electronic Data During Travel
Laptop Loan Program
Deemed Exports
Publicly Available, Public Domain, Open Source
Educational Information
Fundamental Research Exclusion
International Travel & Data Protection
Export Controls Training
Effort Reporting
Effort Certification
Working with Salary Caps
Video Tutorials
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
