Tag Archives: Health information management; Compliance; Privacy; Confidentiality; IRB checklist; Human participant protection; Institutional review board; and Clinical research

by Lynnda J. Emery, EdD, OTR/L; Carolyn Harvey, PhD, CIH; and Catherine M. Andersen, MPH, RHIA, CPHIMS

Abstract

Developing research proposals that protect human participants and understanding the institutional review board (IRB) approval process require high-level application of many skills.