Forms

Listed below are the most commonly used forms in both Word or Adobe Acrobat format.

Initial Study Application (Sponsor/CRO - Multicenter Study)
Initial Study Application (Investigator - Multicenter Study)
Initial Study Application (Single Site Study)
Initial Device Study Application (Sponsor/CRO - Multicenter Study)
Initial Device Study Application (Investigator - Multicenter Study)
Initial Device Study Application (Single Site Study)
Site Information Form
Site Status Report Form
1572 Equivalent
Adverse Event / Unanticipated Adverse Device Effect Report Form
Unanticipated Problem Involving Risk to Subject or Others Report Form
Research Status Report Form
Research Status Report Form (Sponsor/CRO - Multicenter/Registry Study)
Final / Study Completed Report
Request for Reinstatement of IRB Approval
Request for Partial Waiver of Authorization
Phone Screen Info Form
Waiver / Deference of Review Form
Significant Protocol Deviation/Violation Report Form
Investigator Manual
Experimental Bill of Rights
Experimental Bill of Rights–Spanish

If you wish to view the PDF version of the documents and do not currently have the Adobe Reader installed, you can download it free by clicking the link below.

ABOUT ASPIRE IRB

Aspire IRB was founded in 2004 by dedicated women holding CIP certifications with more than 35 years of combined IRB experience. They were inspired to make a difference in the growing IRB industry. Aspire is a certified women-owned business by the Women's Business Enterprise National Council. During the past four years Aspire IRB has developed a stellar reputation in the industry and their business has increased at an incredible rate. They continue to add professionals to their staff and are poised to continue their growth into the next decade.

Aspire IRB's business philosophy is to build lasting relationships with business partners who are dedicated to research and the ethical protection of human subjects. We are committed to timely and efficient results with an emphasis on communication and teamwork.