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.

Mr. Bonner is consistently ranked among the nation’s top healthcare: pharmaceutical/medical products regulatory lawyers by Chambers USA. Clients are regularly impressed by Mr. Bonner who handles safety, compliance and efficacy issues. They have said “he is a former federal prosecutor and works with the district officers, the inspectors. He knows them all and has credibility with the district offices… we have had some really sensitive quality matters and I needed someone I really trusted. He has been fabulous.” In Chambers USA clients praise him as “one of the best good manufacturing practice and product quality lawyers around.” Within the field, he is very well known for the quality of his representation of clients in relation to government investigations, enforcement proceedings and other related litigation.