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See also:

Discovery Alliance : Clinical Trials Management

eTrialTrak : Clinical Trials Applications

 

Regulatory Submission Packets

Effective May 1st, 2007 all submissions must be made electronically through eIRB.  For more information, see eIRB.

Regulatory Submission Support Documents are available below in PDF and Microsoft Word format.  If you prefer to have documents mailed to you, or if you have additional questions, please contact Kellie Andrews by phone at 251-479-5IRB (5472) or e-mail info@pacirb.com .

Regulatory Submission Support Documents

Files are available in PDF and Microsoft Word format.
Note:  You may be prompted for a password when you attempt to open the Microsoft Word documents.  Simply click "cancel" and the form will open.

 

Investigator Handbook PDF Microsoft Word
Additional Site Questionnaire PDF Microsoft Word
Sample Informed Consent PDF Microsoft Word
Sample Submission Letter

PDF

Microsoft Word
Application for Waiver of Authorization

PDF

Microsoft Word

 

 

Compass Point Research. Inc.

Copyright © 2007 Patient Advocacy Council, Inc.