Does the IRB need to review my study?
If your research involves human subjects or is regulated by the Food and Drug Administration (FDA), it requires review and approval from an institutional review board (IRB). Start by answering these questions:
- Is it human subjects research?
- Is your project a systematic investigation designed to produce generalizable knowledge?
- Will your research collect information or specimens from living individuals through interaction or interventions?
- Will you collect, use, analyze, or create identifiable information or biospecimens about living individuals?
- Is it research involving the FDA?
- Does the research involve the study of a drug, biologic, or device regulated by the FDA?
- Will research data be reported to the FDA?
If you answered yes to 1 or 2 above, then your study requires IRB review and approval.
If neither 1 or 2 apply to your project, please consider whether your project might qualify as Not Human Subjects Research or Quality Improvement. You may contact the IRB office for additional guidance.
Who can be a Principal Investigator?
All KUMC and KULC faculty may exercise the privilege of being named as principal investigator (PI) or project director on proposals. University or hospital staff may qualify to serve as PI when approved by the appropriate chair, dean, center director or hospital administrator. Qualifications for PIs are determined by the HRPP in consultation with institutional leaders.
Faculty members from affiliated institutions may be approved to serve as PI for a KUMC project on a case-by-case basis.
For more detailed information about PI responsibilities visit IRB SOP 18.0.
What training is required?
All KUMC research personnel, KUMC staff, affiliated staff and collaborators from other institutions who participate in human subjects research at KUMC must pass and maintain current Human Research Protection training. KUMC partners with CITI (Collaborative Institutional Training Initiative) to provide Human Research Protection training. Training must be renewed every three years.
Research personnel should complete either the Biomedical Basic Course or the Social-Behavioral Basic Course, depending on the type of research activity planned. Advanced courses may be required if research involves vulnerable populations. For research personnel who previously completed Social-Behavioral training and are now involved in biomedical research, an additional course "FDA Research for Social-Behavioral Investigators" will satisfy this requirement.
The CITI system also is used for training in Good Clinical Practice (GCP) and Responsible Conduct of Research (RCR), if applicable. However, GCP and RCR training are separate requirements and can NOT be substituted for the Human Subjects Protections requirement.
Detailed information on how to access, complete and verify training can be found in the CITI Guide to Getting Started. While it is important to complete your CITI training for Human Research Protection and Conflict of Interest in a timely manner, we ask that you wait until you have access to eCompliance before you log into CITI. Once you are able to log into eCompliance, you can log into CITI and click on the LOG IN THROUGH MY INSTITUTION link.
The Research Institute provides additional training information and guidance on RCR and GCP training or you may contact Mary Hindle.
What level of IRB review is required?
At KUMC there are 5 IRB review and application types:
Flexible IRB Review
Projects that are minimal risk and are not associated with federal funding or support may qualify for Flexible IRB Review. Examples include behavioral interventions or minimal-risk biomedical procedures. Flexible IRB review allows abbreviated IRB applications and consent forms, streamlined review by IRB Chair or staff members and elimination of the continuing review requirement. Visit Flexible IRB Review for more detailed information.
Secondary research involves the analysis of data or specimens that have been or will be collected for non-research purposes. Secondary research may also include analysis of data or specimens that were collected under other research protocols. Examples include chart reviews, use of existing specimen repositories, and big data research.
Exempt research involves low risk studies, federally funded or supported, that meet criteria specified by federal regulations. Examples include online surveys, interviews and focus groups, and research on education or curricula.
Expedited research includes studies, federally funded or supported, that meet specific categories in the federal regulations and involve no greater than minimal risk. Expedited review procedures allow the IRB to review without convening a full IRB meeting. Examples include analysis of non-invasive collection of biospecimens, MRI studies, creating a data registry or repository for future studies, or minimal risk behavioral interventions.
Full-board studies are those that do not qualify for any of four categories above. These studies are reviewed at convened board meetings. KUMC IRB meetings occur four times monthly.
Two charts provide additional help to select the appropriate application form:
Where do I submit a proposal?
Research proposals are submitted through our electronic IRB system called eCompliance. eCompliance houses all IRB review activities and serves as the official source for all IRB-approved documentation.
- KUMC faculty or staff members can access the system using their KUMC username and password.
- For dually-appointed personnel, please choose the campus with which a specific project is associated and then login with those credentials
- KUMC students may need accounts enabled by the system administrator if they have not served on previous studies. Please contact the Office of Compliance for assistance.
- For individuals affiliated with KUMC research, but not an employee or student at the University, please contact your principal investigator (PI). The Account Requestor list by KUMC Department will help the PI identify your contact to request an account.
Detailed instructions for how to prepare documents, access, navigate and submit within the eCompliance system are provided in the eCompliance Guidance document. Departmental training and eCompliance assistance can be arranged by contacting the IRB Office.
What documents are required for an IRB submission?
Submission requirements are tailored to the type of IRB submission. Users will answer basic questions on the 'Smart Tabs' of the electronic application and upload key documents into the relevant tabs. The list of Documents to Prepare guides the study team about which items should be uploaded into eCompliance.
When does the HIPAA rule apply to my research?
The Health Insurance Portability and Accountability Act of 1996 (HIPAA) is a federal law that provides safeguards that protect patient privacy. HIPAA requirements are tailored to the type of research and may affect data collection, data sharing, recruitment, informed consent, and collaborations with external entities.
Visit the KUMC Privacy Program for more detailed instructions.
Where can I find guidance about recruiting participants?
Recruitment resources coming soon!
Does KUMC allow the use of external IRBs?
Yes. KUMC has multiple relationships with external IRBs including commercial IRBs and IRBs at other academic institutions through the SMART IRB network. There are special application forms and consent form templates when using external IRBs. Visit KUMC IRB Reliance Resources for additional information about the types of IRB reliance and how to request use of external IRBs.
Aug 20, 2020