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FDA / OHRP IRB Compliance
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Investigator Handbook
Regulatory Forms for Trials Started Prior to May 1, 2007
New Submissions and Studies Opened After May 1, 2007
Printable Version of
Board Members

See also:

Discovery Alliance : Clinical Trials Management

eTrialTrak : Clinical Trials Applications

 

eIRB - Electronic Submissions

Effective May 1st, 2007 all new submissions must be made electronically through eIRB

Please review the registration and submission guidelines for eIRB. Should you have questions or require additional information, please contact one of our representatives at [251] 479 5472.

 

4 PAC IRB Sample Informed Consent Form - WORD

(IMPORTANT: Submissions containing consent forms not submitted in the specified outline of the sample ICF will be returned.)



 

 
 

 

 

 

 

 

 

 

Compass Point Research. Inc.

Copyright © 2007 Patient Advocacy Council, Inc.