M. Jason Brooke

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Epstein Becker & Green, P.C.

M. Jason Brooke is an Associate in the Health Care and Life Sciences practice of Epstein Becker Green in Washington, DC. Mr. Brooke assists medical device and pharmaceutical companies with FDA regulation compliance and quality systems risk assessment, advises drug and device developers on clinical research and counsels foreign medical device companies on U.S. regulatory and reimbursement strategies.

Before joining EBG, Mr. Brooke was a program analyst for the FDA’s Center for Devices and Radiological Health in Rockville, Maryland, where he reviewed proposed and final rules and guidance documents for regulatory compliance.

Mr. Brooke also has considerable scientific research experience, including serving as a Senior Research Scientist at a manufacturer of cardiovascular products in St. Paul, Minnesota, where, among other things, he planned, developed, coordinated, and analyzed results from U.S. and foreign clinical trials to develop automaticity features for implantable cardiac devices.

While attending the University of Maryland School of Law, Mr. Brooke was the Editor-in-Chief of the Journal of Health Care Law & Policy.