260585 Research vs. Public Health Practice Update: How to Assure a High Quality, Safe and Ethical Practice?

Monday, October 29, 2012

Robert DeFraites, MD, MPH , Department of Tropical Medicine, Uniformed Services University of the Health Sciences, Bethesda, MD
Jean Otto, DrPH, MPH , Armed Forces Health Surveillance Center, Silver Spring, MD
Scientific and clinical activities undertaken by public health agencies may be misconstrued as medical research. Most discusssions of regulatory oversight of medical research activities are focused on research activities undertaken either in the setting of clinical practice or in clinical trials in which healthy volunteers are enrolled. Little regulatory attention has been paid to differentiating those scientific activities at the core of public health practice from identical practices undertaken in the course of pursuing medical research. This gap has caused some degree of confusion and uncertainty for public health agencies at all levels of government, including the Federal sector. We will discuss how one can adjudicate and support activities common to public health and research investigations, including the question of if, when, and how institutional research review boards should become involved. We will also suggest management mechanisms to assure high quality and ethical public health practice.

Learning Areas:
Ethics, professional and legal requirements
Public health or related laws, regulations, standards, or guidelines
Public health or related research

Learning Objectives:
List 3 characteristics common to research endeavors and public health practice. Differentiate between public health practice and research.

Keywords: Ethics, Public Health Research

Presenting author's disclosure statement:

Qualified on the content I am responsible for because: From 2007-11 I directed the Armed Forces Health Surveillance Center, responsible for collection, analysis, and reporting of vital statistics for the Department of Defense and US Coast Guard. These responsibilities included management of the Defense Medical Surveillance System for tracking health status of all US military service members and research, mission permitting. These data include personal health information, the handling and disposition of which require compliance with privacy and HIPAA legal and regulatory guidance.
Any relevant financial relationships? No

I agree to comply with the American Public Health Association Conflict of Interest and Commercial Support Guidelines, and to disclose to the participants any off-label or experimental uses of a commercial product or service discussed in my presentation.

Back to: 3282.0: Poster Session I