IRB Forms and Templates
If you need more guidance, visit our page on Submitting an IRB Protocol for step-by-step instructions.
IRB APPLICATION FORMS
All studies submitted to the UTA IRB for review must complete & upload one of the following two application forms:
- Initial IRB Application for Primary Research Studies - updated as of July 7, 2020: This IRB Application Form must be used for all studies that will involve "primary research," defined as: the collection of new information or biospecimens from human subjects for research purposes via:
- interaction with the individual, which includes any form of interpersonal contact between the investigator(s) and the subject (including over the internet!); and/or
- intervention with the individual, which includes both physican procedures by which information or biospecimens are gathered, as well as manpulations of the subject and/or his/her environment.
- Initial IRB Application for Secondary Research ONLY: This IRB Application Form is used for studies that will only conduct “secondary research,” defined as: use of private identifiable information or identifiable biospecimens that have been (or will be) collected or generated for non-research purposes, or from research studies other than your current proposed study.
INFORMED CONSENT TEMPLATES
Consent for Adults: All risk levels
Condensed Consent for Adults: Minimal Risk only
Federally Funded Biomedical or Clinical Trials with Adults: Federally Funded only
Consent for Parents and Children: All risk levels
WAIVER OR ALTERATION OF INFORMED CONSENT
NON-UTA COLLABORATOR DOCUMENTS
SUPPLEMENTAL FORMS FOR STUDIES USING MEDICAL DEVICES AND DRUGS
VULNERABLE POPULATION SUPPLEMENTAL FORMS