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April 15, 2019 - RAPID a real time platform for knowledge management and data analytics

Henry “Skip” Francis, MD

Associate Director for Data Mining and Informatics Evaluation and Research, Office of Translational Sciences, Center for Drug Evaluation and Research (CDER), Food and Drug Administration (FDA)

Monday, April 15, 2019
12:00 – 1:00 PM
1149 Public Health

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The Real-Time Application for Portable Interactive Devices (RAPID) is an Amazon cloud-based system designed which functions as a Saas and Paas system to receive electronic information, analyze it and respond to the sender of the information within 24 hours. The modular system accepts a variety of data types which may be evaluated by internal federal data analysts in real-time. The bidirectional design permits the transmission of timely emergency information to health care providers or other individuals during public health emergencies.

About the speaker:

Henry Francis MDFrom March 11, 2013 to the present, Dr. Francis is the Director of the Data mining and Informatics Evaluation and Research Group in the Office of Translational Sciences, CDER, FDA. In that capacity he directs a trans-disciplinary group of senior sciences to test, create and operate data analysis program facilitating the efficient use of scientific methods to evaluate complex data information in order to make regulatory decisions for drug approval and drug safety.

From October of 2007 until March 10, 2013, Dr. Francis was the deputy director of the Office of Surveillance and Epidemiology (OSE) in the Center for Drug Evaluation and Research (CDER) in the Food and Drug Administration (FDA). Dr. Francis works with the OSE director to lead 5 divisions of pharmacy and clinical scientists in the detection and study of adverse medical events (AE’s) occurring after the release of new drugs into the American health market, also called the post market period. Dr. Francis’s specific interest is in the development of data mining techniques to enhance pharmacovigliance capabilities in national medication use and health care databases.

Prior to working in FDA, Dr Francis was a basic and clinical researcher in the National Institute of Allergy and Infectious Diseases in the National Institutes of Health (NIH). As an AIDS clinical investigator, he worked in several clinical and epidemiologic research projects conducting AIDS and tropical research projects in the Democratic Republic of the Congo (DRC, formerly known as Zaire) and other projects in the Caribbean and the South Pacific. In the DRC, Dr. Francis was the Director of the U.S. Public Health Service & Belgian Project SIDA (AIDS research) Research Laboratories in Kinshasa, DRC.

Dr. Francis served as the first Director of the National Institute on Drug Abuse’s (NIDA) Center on AIDS and Other Medical Consequences of Drug Abuse (CAMCODA). As a clinician, Dr. Francis was an assistant professor of medicine at the Johns Hopkins University School of Medicine’s Division of Infectious diseases where he served as the Principal Medical Officer of the Broadway Women’s Drug Use Center and as the Ryan White Title III investigator and medical Director of the Baltimore City Department of Health’s Sexually Transmitted Diseases clinics.


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