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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
Institutional Animal Care and Use Committee
Institutional Biosafety Committee
Conflict of Interest
Disclosure Instructions
Procedures
Outside Compensated Services
COA Request Instructions
Reviewing Requests
Navigating COI and Related Regulations
Financial Conflicts of Interest
External Relationships
Paid Travel
Impacts on Students
Conflict of Interest Training
Responsible Conduct of Research
Research Misconduct
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U.S. Export Controls
Overview of Regulations
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Research Compliance
International Shipping
Foreign Workers and Visitors
Restricted Party Screening
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Recordkeeping Requirements
Reporting Violations
Protecting Electronic Data During Travel
Laptop Loan Program
Deemed Exports
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Fundamental Research Exclusion
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Export Controls Training
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Completing a first-rate review: Your responsibilities as an IRB reviewer
