On April 13, Polsinelli Public Policy practice member Cybil G. Roehrenbeck
will present at the Food and Drug Law Institute (FDLI) Introduction to Medical Device Law and Regulation conference in Washington, DC. This in-depth, interactive two-day seminar is beneficial for new professionals in the medical device industry and seasoned regulatory affairs or legal professionals looking for a refresher on current FDA medical device policies and practices. Attendees will have the opportunity to interact with subject matter specialists who will review the essential elements of medical device regulation.
Coverage, Coding and Payment – Collaboration between FDA and the Centers for Medicare and Medicaid Services (CMS)
April 13, 2016 | 8:35 - 9:20 AM
Cybil’s session will examine key coverage and reimbursement issues for new medical device innovations. Specifically, she will discuss the need for data to show clinician use of innovative devices and improved patient health outcomes; distinguishing elements of FDA and CMS requirements; and best practices for obtaining appropriate Medicare coverage.