Follow the step-by-step instructions below to successfully prepare and submit a protocol to the IRB. Instructions below include information about single IRBs, student involvement in human subject ...

All research involving human subjects that does not qualify for Exempt or Expedited review is reviewed by the convened IRB. For example, convened review is required for all research that involves ...

No. All human subject research conducted by undergraduate students, graduate students and postdoctoral fellows require a faculty or staff member to serve as principal investigator. This faculty or ...

1. Investigators have not completed required CITI training courses/ modules. See the HRPP Required Training webpage for guidance. Note that if you have taken a CITI course elsewhere, you must ...

Several preliminary steps must be completed before the IRB can review any application. Completing these steps as described can help investigators avoid delays in receiving review by the IRB.

When should you submit your IRB protocol submission? It is important to plan ahead and submit your IRB protocol submission ahead of time so it can be reviewed, processed, and approved by the CWRU IRB.

Institutional Biosafety Committee – recombinant DNA, materials of human or non-human primate origin, toxins, select agents, etc. Radiation Safety Committee – radioactive materials Institutional Review ...

For more information, contact Janet Cline, Director of Research Integrity and Compliance, at 606-783-2541. NOTE: All researchers/investigators who submit a research ...

The Purdue University Institutional Biosafety Committee (IBC) reviews research protocols involving the use of recombinant DNA (rDNA), synthetic nucleic acids, and/or biohazardous agents that present a ...

The future of clinical research depends on people just as much as strong systems and processes. Learn what makes great ...