Raymond A Bonner

Practice Areas

RAYMOND A. BONNER founded the firm’s Food, Drug and Medical Device practice and was a member of the firm’s Executive Committee from 2008-2022. He concentrates his practice on representing life science companies in connection with government investigations, enforcement proceedings and litigation. These investigations and related enforcement matters involve a range of matters including clinical studies, marketing practices, pricing and reimbursement, product safety and reporting, good manufacturing practices (GMP), quality system regulation (QSR), and HACCP.

Prior to joining Sidley, Mr. Bonner served as an Assistant United States Attorney in the District of Maryland for six years, where he prosecuted pharmaceutical application and GMP cases and litigated other FDA-related cases. Throughout his tenure as a prosecutor, he counseled FDA and its Special Prosecution Staff investigating the healthcare industry.