About Harrison IRB Information on Harrison IRB Sponsors Harrison IRB is commited to protecting the Rights and Welfare of research participants Harrison IRB News and Events Current Jop Openings with Harrison IRB People and Departments to Contact at Harrison IRB  
 
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Investigators are an integral part to clinical research. Harrison IRB wants to provide a stress-free service to investigators who decide to conduct research at their sites. Our processes and forms are user-friendly to allow your research staff to focus on all of the various aspects of study start-up and to allow Harrison IRB to process your documentation in a timely manner and error free.

If you have any questions regarding Harrison IRB’s site documents or need assistance with completing a form, please contact our office at 740.845.0814. You may also contact us at info@harrisonirb.com.

Please review the submission requirements timeline document to ensure compliance when submitting IRB reports to Harrison IRB.

 

      
Quick links to Forms
Site Submission Forms
Investigational Studies
 
Site Submission Forms
Post Marketing Studies
 
Additional Clinical Research Information Links
 
Additional Documents Throughout the Study

FDA Site
 HIPAA Guidance
Financial Disclosure by Clinical Investigators
California Experimental Subject's Bill of Rights (Section 24172)
California HIPAA Requirements
Disclosure of Prior IRB Reviews
Recruiting Study Subjects
Informed Consent Guidelines

 

Advertisement Submission Form
Site Information Change Request Form
Continuing Review Reporting Form
Close Out Reporting Form
Protocol Deviation Reporting Form
Serious Adverse Event Reporting Form
Unanticipated Problems Reporting Form
Unanticipated Problems Fact Sheet
IRB Reporting Requirements for Sites
   
 

Specialty Documents