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Browse the definitions of technical terms in the Policy Manual
For Researchers & Affiliates
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Clinical Trials Study Management
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Sample Data Safety & Monitoring Plan Outline
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Clinical Trial Requirements
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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
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Completing a first-rate review: Your responsibilities as an IRB reviewer
