Medical device risk managers, register today for Medmarc’s Tuesday, 5/29/18, 2 PM, ET webinar: “Big Legislative Changes, What You Need to Know to Meet the New Compliance Challenges.” Presenter Steven Niedelman will discuss FDARA and the 21st Century Cures Act—legislation likely to have serious effects on device companies. Failure to comply may make companies vulnerable to shut down. Learn how to prepare for new requirements.
Register here. Visit Medmarc’s schedule for upcoming and prior risk management webinars on a range of life sciences and medical devices products liability topics.