Recent changes to European regulations have sparked a lot of interest and intrigue, and even more questions. So, what specifically do medical device companies need to know about these MDR and TF changes? In this webinar recorded on 6/2, Rook’s own resident MDR experts, Quality Managers Jakemia Barnette and Chandler Thames, expand on the nuances of the transition, and provide key insights and guidance.
Have questions for our team? We’re here for you.