UNC Research

Sample Consent Forms

Consent form templates.

These consent form templates have been posted for your reference.  When completing and IRB submission in IRBIS, please fill in the application and use the consent form builder specific to your project.  For more information, please find instructions here .

Summary of Changes to the Regulations for Informed Consent:  Revised Common Rule Changes to Informed Consent and Waiver Requirements

Summary of Changes to Consent Documents:

  • Informed Consent Documents – Version 2.0 Summary of Changes
  • Informed Consent Documents – Version 2.1 Summary of Changes
  • Informed Consent Documents – 10/26/2020 Summary of Changes
  • Informed Consent Documents – 4/10/2023 Summary of Changes
2023-07-14
2020-01-17
2020-01-17
2020-01-17
2023-04-10
2023-06-27
2023-04-10
The following documents are samples.
IRBIS does NOT generate these documents with application-specific information.
2017-10-30
2024-08-09
2017-04-17
2018-04-19

Concise Summary examples can be found here .

Guidance on the use of plain language in consent forms:

  • Clinical Research Glossary
  • Webinar: The Promise of Plain Language: Launching a Glossary to Support Participant Understanding of Clinical Research – Recording & Slides

There are a few additional forms that are not provided online and may be accessed below.  As needed, these should be completed and uploaded to your IRB application.

Foreign Language Consent Forms

COVID-19 Related Forms:

  • Spanish-IRB-COVID Information Sheet
  • Spanish COVID Consent Letter v2
  • Spanish COVID Informational Sheet Translation Certificate

Informed Consent Short Form (for a single subject who may be illiterate, or otherwise unable to read the consent form — used when full consent form has to be read or translated for subject).

  • Informed Consent Short Form Guidance
  • Simplified Chinese

HIPAA Templates

  • Sample HIPAA Authorization Template
  • Sample HIPAA Authorization Template in Spanish ( Certification )