University of Missouri - Kansas City

Vice Provost for Research - Office of Research Services

 

Research Protections Program

Forms and Guides

Please e-mail your submission to andermansh@umkc.edu

Once you have electronically submitted your protocols/continuations requests/SAE/other documents - you will also need to submit 4 signed original hard-copy to the IRB Office. The IRB must receive a hard copy with original PI signature on the application forms before review or action approval can take place.

If all of your documents are not in an electronic format, you may visit the IRB office ( 5319 Rockhill Road) and use our high-speed scanner to scan the documents into a PDF format for submission.

Initial Submission

IRB Application Form

Additional Study Location Agreement

Financial Disclosure

 

IRB Submission FAQs

IRB Submission Checklist
Checklist for completing the Adult Health IRB application including a checklist for submission
Application for Exemption

 

Adverse Event
Adverse Event Form
Form submitted for Adverse Events

 

Amendment

 

Progress Report

Progress Report Form
Form submitted with request for continuing review or final report

 

Informed Consent and working with Vulnerable Populations

Consent Form Template
Genetic Consent Form Template


Informed Consent Form Guidance

Genetic Consent Form Guidance

Glossary of Medical Lay Terms

IRB Commonly Used Terms and Definitions

 

 

 

Coded Agreement
Office for Human Research Protections (OHRP) issued "Guidance on Research Involving Coded Private Information or Biological Specimens". (10 August 2004)