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James Swiger, MBE, is a Program Official in the Division of Digital Healthcare Research in the Center for Evidence and Practice Improvement at the Agency for Healthcare Research and Quality (AHRQ), where he supports digital healthcare research projects and serves as Team Lead for the Clinical Decision Support Program.

Prior to joining AHRQ, Mr. Swiger worked at the U.S. Food and Drug Administration in the Center for Devices and Radiological Health (CDRH). At CDRH, he was a Deputy Division Director in the Medical Product Safety Network (MedSun), a program that collaborated with a volunteer network of medical device user facilities nationwide to identify, understand, and solve problems with the use of medical devices through a customized health IT platform. He was also a lead reviewer for pre-market orthopedic and spine implant submissions and served as a project manager for professional development initiatives in CDRH's Office of Product Evaluation and Quality. Prior to FDA, he was a patent examiner at the U.S. Patent and Trademark Office. Mr. Swiger received his Bachelor’s and Master’s degrees in Biomedical Engineering from The Catholic University of America in Washington, DC.