The rapidly changing legislative, reimbursement, regulatory, and technology landscapes, coupled with increasing civil and criminal liability, have posed significant challenges and offered tremendous opportunities for medical device manufacturers.
To help you address these developments, the Medical Device attorneys of Foley & Lardner LLP provide fully integrated experience in U.S. Food and Drug Administration (FDA) and health care regulatory issues, reimbursement, intellectual property law (IP), business law, litigation, and public affairs, enabling us to collaboratively craft effective strategies and implement them with clients.
Read The Pulse newsletter by clicking on the link below.
