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Submission Forms:
Commitment to the Conduct of a Clinical Trial FormDOC PDF
Process for Obtaining Informed Consent (Courtesy)DOCPDF
Principal Investigator Submission FormDOCPDF
Sub Investigator Submission FormDOCPDF

Initial Protocol Submission Form		DOCPDF
Initial Protocol Submission DefinitionsDOCPDF
Expedited Review Initial Protocol Submission FormDOCPDF
Expedited Review Principal Investigator Submission Form DOCPDF
Expedited Review Sub Investigator Submission Form DOCPDF

Ongoing Reporting Forms
Study Start Notification FormDOCPDF
Site Final Report FormDOCPDF
Sponsor Close Out Report FormDOCPDF
Protocol Deviations/Violations Reporting InstructionsDOCPDF
Protocol Deviations/Violations Report FormDOCPDF
Study Complaint Form (completed by the site)DOCPDF
Investigator Drug Brochure Amendment FormDOCPDF
Request for Amendment FormDOC

Continuing Review Reporting Forms
Continuing Review Principal Investigator InstructionsDOCPDF
Continuing Review Report - Principal InvestigatorDOCPDF
Continuing Review Report - SponsorDOCPDF


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Last Updated on Monday, 10 August 2009 20:28
 
Ethical Review Committee IRB - 14400 East 42nd Street Suite 240 Independence, Missouri 64055
(816) 421-0008