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

 

      
Quick links to Forms
Site Submission Forms
Investigational Studies
Additional Clinical Research Information Links
 
Site Submission Forms

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

 
Post Marketing Studies
 
 
 
Additional Documents Throughout the Study

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
 

Specialty Documents
 
Consent Waiver
Emergency Use Checklist
CA Experimental Subject's Bill of Rights