Forms & Resources
To check boxes in the forms, please double click!
IRB Human Subjects Study Application (fillable PDF) (Human Subjects Application Form)
Adverse Events Form (fillable PDF)
Continuation Request Form (docx)
HIPAA Compliance Form (doc)
Mandated Reporter Form (pdf)
Research Team Form (fillable PDF)
Study Closure Form (docx)
Debriefing Template (doc)
Informed Consent Document (docx)
International Research (docx)
The following e-presentation provides the basics for preparing a successful human subjects research protocol:
- Navigating-the-IRB-2016 (ppt)
The EU General Data Protection Regulations may apply to your research. Please consult the University of Illinois system GDPR Information Page for more details. The Office of Research and Sponsored Programs will evaluate your protocol and provide advice. This article describes the GDPR implications for secondary research, such as public clinical trial data.
Chastain, G., & Landrum, R.E. (1999). Protecting Human Subjects. Washington, DC: American Psychological Association.
Sales, B.D., & Folkman, S. (2000). Ethics in Research with Human Participants. Washington, DC: American Psychological Association.
Other resources to assist with research, grants and contracts, including workshops and tutorials, are available on the UIS Research Resources webpage.