General Clinical Research Center


Initiating An Approved Protocol

  • You will be notified by letter when your protocol is approved by the GCRC Advisory Committee.

  • Send two copies of the IRB-01 approved
    information summaries and consent forms to the GCRC office, 157 MRF.

  • Schedule a joint meeting with the Nurse Manager (353-6250), Research Dietitian, Administrative Manager, and Research Safety Officer to discuss protocol implementation and educate the nursing staff on your study needs.

  • Prepare study materials.  The nursing staff will assist you in designing and developing flow sheets, labels, and other documents.

  • Schedule any special services required for your study.  

  • Then Recruit subjects! The Nurse Manager can assist you with this process.

 

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