IRB & HSPP Information
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HSPP Staff
Stephanie Schemke, B.A.
IRB Analyst, Social/Behavioral/Educational
502-852-4101
Seth Knight, B.S.
IRB Analyst, Biomedical
502-852-2163
Steffany Gayton, BS, CCRP
IRB Analyst, Biomedical
502-852-4535
Michelle Bottorff, BS, CCRC
IRB Analyst, Biomedical
502-852-5987
Beth Kuntz, LPN, CRCC
IRB Analyst, Biomedical
502-852-2162
Cathy Carter, BA, CCRP, CIP
IRB Coordinator
502-852-4098
Sarah Merrill, BSE, MPH
IRB Coordinator
502-852-5541
Lisa D. Schaffer
Associate Director, Research Compliance
502-852-3641
Shereca Duarte
Research Compliance Specialist III
502-852-5992
Christy LaDuke, MA, CIP, CCRP
Director
502-852-2541
Robbi Devers, A.A., A.A.S.
Program Coordinator Sr
502-852-4097
Kristyn Singleton, MPA, CIP
IRB Operations Coordinator
502-852-4094
IRB Committee Chairs
Pete Quesada, Ph.D.
Chair
502-852-5981
Melissa Evans-Andris, Ph.D.
Vice Chair
502-852-3713
Julie Goldman, MD
Interim Chair
502-852-5188
Janice Sullivan, MD
Vice Chair
502-629-5283
Paula Radmacher, PhD
Vice Chair
Philip Rosenbloom, MD
Vice Chair
Accreditation and Compliance Statements
Accreditation
Association for the Accreditation of Human Research Protection Programs, Inc. (AAHRPP) accreditation is a public affirmation of an organization's commitment to protecting research participants. The University of Louisville Human Subjects Protection Program has full accreditation through AAHRPP.
ICH GCP Compliance Statement
The University of Louisville Institutional Review Boards and the Human Subjects Protection Program were accredited by the Association for the Accreditation of Human Research Protection Programs (AAHRPP) in 2005. The University of Louisville IRBs operate in compliance with Good Clinical Practice (GCP)/International Conference on Harmonization (ICH) Guidelines insofar as those guidelines are consistent with the U.S. Food and Drug Administration regulations (21 CFR Parts 50 and 56) and the Department of Health and Human Services regulations (45 CFR 46) pertaining to the protection of human subjects in research.