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.
We’d also like to share with you a notice on the Pennsylvania Supreme Court Ruling on Informed Consent (August 2017) outlining this new ruling. Please contact legal counsel licensed in Pennsylvania, should you have any questions.
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.