FAQs


Frequently Asked Questions

The Clinical Research Administration in the University of Kansas Medical Center Research Institute facilitates new study start-up and activation with Sponsors and CRO's. Myriad questions and issues relating to the local IRB, facilities and processes commonly are brought up during the start-up period. For more information, please contact the appropriate Clinical Trial Project Manager (CTPM) in the Research Institute.

Last modified: Sep 24, 2014
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