Investigators conducting human subjects research should read Investigator Obligations to ensure that they understand their responsibilities as clinical research investigators.
Midlands IRB encourages investigators to adhere to the highest standards of human subject protection when conducting clinical studies. Towards that end, we have compiled a comprehensive GUIDE FOR RESEARCHERS, which provides important information about study site submissions, informed consent, promptly reportable information, and much more.
For electronic submissions of site submission forms, please access your MyConnexus™ account. Please contact us via email or phone (913.385.1414) with any questions about study site submissions or investigator sponsored studies.