Anette has a background as Certified Registered Nurse Anesthetist and has been working with research in the Copenhagen University Hospital Rigshospitalet prior to entering the medical device world. Anette has more than 20 years of experience within the medical device industry and has hold positions at Ambu A/S, Edwards Life Science and Qmed Consulting. Her primary expertise is within the regulatory and clinical pathway of getting a medical device to marked in both the US and EU. She is currently head of the clinical department of neurescue and is responsible for the clinical part of the 510(K) submission and the CE-mark according to the MDR.
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