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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

 

     
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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