Informed Consent Templates
Informed consent templates have been developed to assist researchers in developing a consent form for a research study. The template is only a guide to help researchers and may be subject to change. Please note that IRB members may still request changes to your document.
The revised Common Rule implements January 21, 2019 for new studies. Several templates have been updated to incorporate the revised Common Rule requirements (noted below). Please use the updated templates. To view more detailed information about the revised Common Rule changes, please visit the Revised Common Rule webpage.
- HRP-502 - Template - Minimal Risk Consent Document (Word 28 KB) (updated for revised Common Rule)
- HRP-507 - Template - Consent Document - Short Form (Word 17 KB) (updated for revised Common Rule)
- HRP-517 - Template - Biomedical Consent Document (Word 36 KB) (updated for revised Common Rule)
- HRP-518 - Template - Social Science - Behavioral Consent Document (Word 33 KB) (updated for revised Common Rule)
- HRP-519 - Template - Genomics Consent Document (Word 43 KB) (updated for revised Common Rule)
- HRP-520 - Template - Consent Document for Exempt Research (Word 30 KB)
- HRP-521 - Template - Assent Document (Word 17 KB)
- HRP-522 - Template - Parental Permission Document (Word 22 KB)
- HRP-523 - Template - Telephone Script Consent Document (24 KB) (updated for revised Common Rule)
- HRP-524 - Template - Screening Consent Document (Word 26 KB)
- HRP-525 - Template - Consent Language when using Experimetrix (Word 17 KB)
- HRP-526 - Template - Consent Language when using Sona (Word 18 KB)
- HRP-543 - Template - MRI Screening Form Pregnancy (Word 18 KB)
More Information About the Revised Common Rule (2018 Requirements)
The revised Common Rule requires several changes to the informed consent document. Included below is guidance and help information on these requirements. To view more detailed information, please visit the Revised Common Rule Informed Consent Requirements webpage.