Jennie brings a broad experience from regulatory work within the life science and medical devices industry at PlantVision AB and St. Jude Medical, where she has worked with vigilance, CE marking, global submissions, regulatory strategy, and held courses/seminar in the Medical Device Regulations (MDR, IVDR).
”It feels both important and intriguing to contribute to Stratipaths mission. Getting innovative research into practical use safely is what regulatory work is all about. I am looking forward to working closely with the product development and medical affairs teams to make sure we reach compliance for CE marking for our products.“ Says Jennie.
“In addition to Jennie’s excellence and long experience in the field, we also appreciate her drive and personality, which we believe will be crucial in achieving our mission to improve cancer treatment decisions and patient outcomes.” Says CEO Fredrik Wetterhall
