Forms

IRB Application and Consent Forms

Continuing Review Application for Research Involving Human Participants

Application for Approval to Use Human Participants

Sample Informed Consent Form and Checklist

Training for Researchers

For the required training on protections for human subjects and other ethical issues

For training on the initial submission to the IRBNet.org

For further information, you are encouraged to visit the new OHRP human subject protections resource page at http://www.hhs.gov/ohrp/policy/index.html This page provides links to reference documents, the Code of Federal Regulations 45 CFR 46, historical materials and Common Rule departments/agencies. OHRP encourages all in the research community to use this reference page.