Arthur E. Kim
Associate
Washington, D.C.
Practice Group
Regulatory
As an associate in our Food, Drug, Medical Device, and Agriculture group, Arthur Kim focuses on federal and state medical device regulation. He advises clients on post-market compliance issues, adverse event reporting, field action, and advertising and promotion requirements and also prepares materials for pre-market clearance and approval of new medical devices.
Arthur is also actively involved in the firm's pro bono efforts in education, housing rights, and ยง 1983 claims.
While in law school, Arthur served as senior development editor for the Georgetown Law Journal.
Industries
Areas of focus
Latest thinking and events
Hogan Lovells Publications
Current good manufacturing practice requirements for combination products
Medical Device and Pharmaceutical/Biotech AlertHogan Lovells Publications
FDA Issues Final Guidance on Benefit-Risk Factors to Consider in Medical Device Product Availability, Compliance, and Enforcement Decisions
Medical Device AlertHogan Lovells Publications
FDA Takes Steps to Clarify Significant Human Tissue Questions
Medical Device, Pharmaceutical, and Biotechnology AlertHogan Lovells Publications
Draft Guidance on General Considerations for Animal Studies
Medical Device AlertView More
