What does the new regulatory map look like based on new rules for software classification in MDR compared to MDD? How do I best set up the plan for a reclassification - from class I to class IIa or higher? What does my company need to do right now? Watch our webinar about the new Medical Device Regulation (MDR) and how it will affect healthtech companies.
Speakers:Johanna Fugelstad, Senior Consultant Clinical Evaluations, Key2ComplianceDavid Hedfors, Quality and Regulatory Affairs Director, RaySearch
Did you miss out on the webinar on October 23? Watch it online today!