Institutional Review Board

cure
Wichita Medical Research & Education Foundation Wichita Medical Research & Education Foundation

 

 

ResponsibilityMembersSchedule
WMREF Research Guide (PDF)
WMREF Research Application (download)
IRB Forms (download)Research Definitions Research Regulations

What is an Institutional Review Board?

Responsibility
The WMREF Institutional Review Board (IRB) has been established in accordance with federal law to ensure that human subjects participating in research activities sponsored by or involving a contracting hospital, clinic, or physician's office are protected from undue risks or deprivation of personal rights and dignity. An IRB has the ultimate responsibility to review human subject research and the authority to approve, require modification in, or disapprove such research, unless the activity has specifically been exempted from IRB review.

Dr. James E. Delmore currently serves as Chair of the WMREF IRB. Dr. Ginger French serves as IRB Director. Members of the WMREF IRB serve as unpaid volunteers.

Dr. James E. Delmore
Dr. Ginger French

If you are interested in receiving more information concerning:

  1. the WMREF IRB
  2. the protection of human subjects involved in research; or
  3. would like to become a member of the WMREF IRB,

contact Ginger French, PharmD, CIM, CIP, WMREF IRB Director at 316-686-7172.

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Current members of the Wichita Medical Research and Education IRB:

James E. Delmore, MD Chair
Ginger French, Pharm, D Director
Natalie Sollo, MD Vice-Chair
William T. Braun, MD Vice-Chair

Sue Crockett, MSW
Joe Carrithers, PhD
Charles Schalon, PhD
Robert McKay, MD
Bassam I. Mattar, MD
Paul Harrison, MD
Kari Schmidt, JD
Tom Welk, PhD
Terri Jones, MPH (ASCP)
Donald Vasqiez, DO
Peggy L. Johnson (Alternate)
Ron Rose, JD (Alternate)
Steve Amos, PhD (Alternate)
Jean Turvey (Non-voting member)
Rev. Rocky Meese (Alternate)
Charlotte Jewell, Research Administrative Secretary

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Schedule
Institutional Review Board Meetings are held at 11:30 am in the Corporate Conference Room at Wesley Medical Center.

2007

Wednesday, January 17 Wednesday, July 18
Wednesday, February 21 Wednesday, August 15
Wednesday, March 21 Wednesday, September 19
Wednesday, April 18 Wednesday, October 17
Wednesday, May 16 Wednesday, November 14
Wednesday, June 20 Wednesday, December 12

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WMREF Research Guide
Click here to download the WMREF Research Guide. This file is in PDF format, and requires Adobe Acrobat ® Reader ® to view. If you do not have Adobe Acrobat Reader, you can download it for free by clicking on the following link:

Download Adobe Acrobat Reader

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WMREF Research Application
Click here to download the WMREF Research Application. This file is in Microsoft Word ® (.doc) format. If you do not have Microsoft Word ®, copies of the Research Proposal Application are available by mail. Please contact the WMREF office at 316-686-7172.

IRB Consent Form
Click here to download the IRB Consent Form. This file is also in Microsoft Word ® (.doc) format.

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IRB Forms

Click the links below to download the IRB Forms. The files are all in Microsoft Word ® (.doc) format.

WMREF Application for IRB Waiver of Authorization
WMREF Checklist for IRB Review of Pediatric Research
WMREF IRB De-Identification Certification Form
WMREF IRB Request for Waiver of Consent Form
WMREF IRB Request for Waiver of Documentation of Consent
WMREF Consent Template
WMREF IRB Investigator Summary Form

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Research Definitions

Research: a systematic investigation, including research development, testing and evaluation, designed to develop or contribute to generalizable knowledge.

This includes activities which meet the definition whether or not they are conducted under a program which is considered research for other purposes; for example, demonstration and service programs may include research activities.

Human Subject: a living individual about whom an investigator conducting research obtains data through intervention or interaction with the individual, or identifiable private information.

Clinical Investigation: any experiment that involves a test article and one or more human subjects.

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Research Regulations

Helpful IRB Website Links

The Belmont Report Declaration of Helsinki
OHRP Decision Charts Federal Regulations and Policies
FDA Information Sheets OHRP – IRB Guidebook
Good Clinical Practice Guidelines NIH – Bioethics Websites
IRB Forum Links Human Subject Protection Tutorial - KUMC
Informed Consent Tutorial – U of Minnesota Research Categories – Expedited
Medical Terms Wichita Medical Research and Education Foundation

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Medical Research is not a solitary endeavor. Your gift of: membership dues, endowment gifts; memorials; bequests provides many opportunities for us to gain knowledge to improve the chances for all of us to live longer, happier, healthier lives. Contact Peggy L Johnson, Executive Director, 316-686-7172.

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