MDR Transition and Technical Files: What You Need to Know
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.
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