Lawyer profile for USA 2022
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Healthcare: Pharmaceutical/Medical Products Regulatory - District of Columbia
This content is provided by Raymond A Bonner
RAYMOND A. BONNER founded the firm’s Food, Drug and Medical Device Compliance and Enforcement practice and is a member of the firm’s Executive Committee. 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’s experience includes:
•Regularly visiting manufacturing sites throughout the world to provide regulatory and compliance support regarding GMP and QSR matters
•Representing companies in connection with Foreign Corrupt Practices Act investigations and compliance programs, trade secret issues, and commercial matters
•Assisting clients with complex non-conforming product, corrective and preventive action (CAPA), data integrity and product impact investigations