- Informed Consent for Non-Medical Research (General)
- Informed Consent Template for Non-Medical Research (Parental Permission)
- Information Sheet for Exempt Research
- Information Sheet for Expedited Research (Requesting a Waiver of Signed Consent)
-
Experimental Subject's Bill of Rights (Word)
(Note: If your study involves a medical procedure, this document must be attached to the front of the Informed Consent document for subjects to sign. Additional non-English translations are available on the Health Sciences IRB website.) - Significant New Findings Template (NEW)
- Model IRB Applications
- Research Site Permission Template
- IRB Authorization Agreement
- Research Consultant Non-Engagement Agreement
- Unaffiliated Investigator Agreement
Independent Translation Services for Informed Consent Forms
The University Park IRB (UPIRB) does not offer translation services for informed consent documents. However, provided below is a list of independent, fee based translation services that investigators can utilize but must bear all cost associated with the service.
Additional Human Subjects Research Information and Guidelines for UPC
There are additional information and guidelines that are available to assist investigators in preparing their IRB applications and in conducting research with human subjects. Please refer to the following information:
- Significant New Findings Policy (NEW)
- Policy Concerning Human Subjects Research at the Dana & David Dornsife Imaging Center
- Classroom and Student Research Procedures (PDF)
- Criteria for Advertisements (PDF)
- The Research Advisory Panel of California (California requires proposed research projects involving certain opioid, stimulant, and hallucinogenic drugs classified as Schedule I and Schedule II controlled substances to be pre-reviewed and authorized by the Research Advisory Panel of California in the Attorney General's Office.)