Forms and Templates

• Listing of eIRB Changes
  
  
• eIRB Changes Attachments
  
  
• Contact the Research Compliance/IRB Office if you have any questions or concerns about these changes.

Submission Review Tool for PIs and Study Staff
Please note that the Research Compliance Office/IRB Staff has developed a submission review tool.  This tool was created to assist Principal Investigators and Study Staff with assessing and addressing study related information prior to sending submissions to the Texas Health Resources IRB. The primary goal of this tool is to assist with accelerating the time it takes for a Principal Investigator to receive IRB final approval of a submission.


FORMS:

• A6 - Preparatory to Research Investigator Representation/Assurance



• A7 - Decedent Information Investigator Representation/Assurance



• A8 - Limited Data Set Representation



• A9 - De-identified Information Investigator Representation/Assurance



• Confidentiality Agreement



• FORM 1-A Drug-Device Questionnaire
  (Required when submitting a study that will be conducted at Texas Health Dallas)



• FORM 1-B New Investigational Drug Fact Sheet
  (Required when submitting a study that will be conducted at Texas Health Dallas)



• IRB Form Bill 1

• Verification Form for Research Investigators and Research Study Staff
  
  Policies Verification Form
       PDF      Word Doc

TEMPLATES:

• A3 - Psychotherapy Authorization Template



• A4 - Repository Research Authorization Template



• CV/Resume Template



• HIPAA/Privacy Authorization Template



• Informed Consent Form Template       Revised Version Effective July 20, 2011
  
  Notable Changes to the Informed Consent Form Template
  
  
• Protocol Template       Effective May 3, 2011
  (To be used as guidance for investigators that do not have a formal protocol and for submissions that the Board deems as having insufficient protocol information)
  
  
  
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