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Browse the definitions of technical terms in the Policy Manual
For Researchers & Affiliates
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Sample Data Safety & Monitoring Plan Outline
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HIPAA and Human Subjects Research
Obtaining Human Research Data Under HIPAA
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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
