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Home
SACHRP
Informed Consent
Special Populations
Recruitment
Clinical Trials
Research Considerations
Reliance/Collaborations
Privacy/Confidentiality
IRB Review Considerations
FDA
Information Sheets
FAQ
Guidance
OHRP
Informed Consent
Special Populations
Research Considerations
Reliance/Collaborations
Privacy/Confidentiality
IRB Review Considerations
NIH
DoD
HRSO
Informed Consent, Assent, and Broad Consent
OHRP Exculpatory Language in Informed Consent (1996) _ HHS.gov.pdf
OHRP Informed Consent Checklist (1998) _ HHS.gov.pdf
OHRP Informed Consent FAQs _ HHS.gov.pdf
OHRP Informed Consent of Subjects Who Do Not Speak English (1995) _ HHS.gov.pdf
OHRP Informed Consent Posting Instructions (2022) _ HHS.gov.pdf
OHRP Informed Consent Requirements in Emergency Research (OPRR Letter, 1996) _ HHS.gov.pdf
OHRP Informed Consent, Legally Effective and Prospectively Obtained (OPRR Letter, 1993) _ HHS.gov.pdf
OHRP Informed Consent Tips (1993) _ HHS.gov.pdf
OHRP Research under FDA's In-vitro Device Interim Final Rule (2006) _ HHS.gov.pdf
OHRP Use of Electronic Informed Consent_ Questions and Answers _ HHS.gov.pdf
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