Objectives

1. Apply the components of a good research question when considering study design
2. Define research, clinical trial, human subject, and identifiable biospecimen/identifiable private information
3. Recognize IRB reviews that will be impacted by revisions to the common rule
4. Identify regulation based resources available to the research community

Faculty

Susan Garrow-Sloan, RN, BSN, CCRP
Human Research Protection Program Education and Compliance Specialist
Office of Research
University of Massachusetts Medical School-Baystate
Baystate Medical Center

None of the members of the faculty and planning committee for this educational event have commercial relationships with any entity producing, marketing, re-selling or distributing health care goods and services consumed by or used on patients.