Forms

Please include the following documents in your online application:
Please prepare the following materials for your online submission:

 

  1. Study Protoco
  2. GCRC Application  *
  3. Biosketches
  4. Flow sheet *
  5. IRB Application *
  6. IRB approved consent form
  7. RB approval letter
  8. IRB approved key personnel list- after your application has been approved, please add the
    GCRC to your key personnel list. You can add it just like adding a person. The IRB has a current
    listing of our staff on file.
  9. Inclusion/exclusion criteria checklist *
  10. Extramural funding award notice *

* All starred documents are required for the protocol to be reviewed. If you do not yet have
IRB approval the protocol can be considered. Any changes suggested by the IRB
must also be incorporated into your GCRC application. Before the study can commence
all IRB related forms must be approved and on file with the GCRC administrative office.
If you have questions about this process, please contact Abby Cosentino for further information.

If you need to edit your documents after your submission, you may do so any time by logging into our online submission system.

   
Other UK GCRC Forms
     
  NIH Policy for Data and Safety Monitoring  
  Further guidance on a Data Safety and Monitoring for Phase I and Phase II trials  
  GCRC Patient Registration Form  
  The Data and Safety Monitoring Board Charter
  Need download Adobe Reader? Click Here
   
Human Subjects Forms
  UK Position on Human Subjects Protection 091905
NIH Forms
  NIH PHS 398 Forms and Instructions
 
NIH logo The UK GCRC is funded by National Center for Research Resources
National Institutes of Health     M01 RR02602