IRB Forms and Guidance Documents
Members of the SUNY Oneonta community who intend to conduct research involving human subjects should complete the IRB Review Form early in the research design phase and submit the form via the PACS module: https://pacsprd2.rfsuny.org
Along with the form, you will be required to submit:
- Consent document
- Assent document (if applicable)
- Questionnaires to be used
- Site approval (if research is occurring at another location)
- Appropriate signatures.
Formal follow up is required on research projects within one year of original approval date.
In preparing their IRB Review Forms, faculty/staff and student researchers should be reminded that particular attention is given to the consent process, which typically requires written consent. Please consult the Consent Form Help Document for guidelines on and examples of written consent forms.
An Investigator’s Guide to Research with Human Participants (subjects) is available for more information to assist investigators in designing Human Subjects research and preparing information to be submitted in the IRB Review Form protocol application.
Questions regarding these processes should be addressed to the IRB mailbox at IRB@oneonta.edu or the Sponsored Programs Office 607-436-2525 or 2473 or the IRB Chair.