Sandra Balseiro and João Quintas participated on the Webinar: Understanding Medical Devices Regulation. This event was an opportunity to deepen knowledge of medical device regulation.
Sandra Balseiro covered the essential steps required for CE marking, highlighting key milestones and outlining the necessary procedures for obtaining CE marking on medical devices and in vitro diagnostics.
João Quintas discussed technical and usability requirements according to the MDR, using case studies of ORACIA and FaceRehab to illustrate real-world applications and challenges under the Medical Devices Regulation.
In addition, Célia Ludovino, from BHL-Medical, Indústria de Produtos Hospitalares, Lda, shared her success story in the transition from Directive 92/43/EC to European Regulation 2017/745. And Ana Abreu, from Kinetikos Health, provided insights about her experience of mastering European Regulation 2017/745 for the first time.
Don’t miss this learning and networking opportunity! Join us at Medical Devices Regulatory — support unit (MDRu) and let’s explore the world of medical device regulation together: https://lnkd.in/dt4tQYNy