The KUMC Human Research Protection Program is responsible to the federal government for all human subjects research conducted by our faculty, staff or students, regardless of whether it is on our campus or in collaboration with another institution.
Faculty who are collaborating on research outside KUMC must obtain approval for their activities before starting work on the project. In times past, IRB approval from each involved institution was required. Recently, however, the federal government has been encouraging arrangements by which collaborative research can be reviewed and approved by one lead IRB when the proper legal agreements are in place. Investigators are encouraged to contact the HSC / IRB Office early in the process of establishing their collaboration. We are committed to working with investigators to negotiate a single IRB review whenever feasible.
These forms shoudl be used when the research is minimal risk and involves Via Christi, Wesley Medical Center, or Wichita State University.
KUSM-W studies involving Via Christi and/or Wesley Medical Center will be submitted via email to email@example.com (in addition to the hosipital's IRB office.)
KUSM-W studies involving only Wichita State University must be submitted in the eCompliance system.
KUSM–W has a reciprocity agreement with Via Christi Hospitals Wichita, Inc. (VCH-W) Institutional Review Board (IRB) which states the KUSM–W IRB can rely on the review of the Via Christi IRB for minimal risk, cooperative research. The Common Form Applications must be submitted via email/paper.
KUSM–W has a reciprocity agreement with Wichita Medical Research & Education Foundation (WMREF), the Institutional Review Board (IRB) for Wesley Medical Center, which states one IRB can rely on the review of the other IRB for minimal risk, cooperative research. The Common Form Applications must be submitted via email/paper.
KUSM-W has a reciprocity agreement with Wichita State University, which states the WSU IRB can rely on the review of the KUSM-W IRB for minimal risk, cooperative research. The Common Form Applications must be submitted in the eCompliance system.
KUMC is responsible for research conducted by our graduate students regardless of where it takes place. KUMC distance learners who conduct their master's or doctoral research at their home institution should consult with their advisors and with the IRB Office as the project is being developed. Single IRB review is generally feasible.
KUMC investigators have the option of using Western IRB for Phase III or Phase IV multi-center, industry-sponsored drug or biologic trials. Additional information is available from the HSC / IRB Office.
The KUMC IRB will work collaboratively with other IRBs as needed to develop protocol-specific reliance agreements. Please consult with the IRB office as soon as you identify a need to engage an external IRB.
When individuals from non-profit organizations, school districts or community groups serve as study personnel on KUMC research, their employers may not typically conduct research and may not have their own IRB. KUMC often serves as the IRB in these circumstances. KUMC investigators should contact the HSC / IRB Office to determine how best to meet the regulatory requirements for our community partners.