Medical Device Regulation and Litigation Conference: Case Study on Medical Device Recalls and Post-Market Reporting
Bradley Merrill Thompson, a Member of the Firm in the Health Care and Life Sciences practice, in the Washington, DC, office, presents "Case Study on Medical Device Recalls and Post-Market Reporting" at the Medical Device Regulation and Litigation Conference.
The conference features an advanced-level discussion among top officials from FDA's Center for Devices and Radiological Health (CDRH), on the most significant recent and upcoming medical device compliance, regulatory, and enforcement priorities. Participants will respond to the Center presentations and attendees will have a unique opportunity to directly ask questions of these Center officials. The conference will also focus on three hot topics: the 510(k) clearance process; risk management strategies for manufacturers; and the use of social media to communicate with end-users.
For more information, visit FDLI.org.