Vida Sollanek

Vida Sollanek is a skilled regulatory affairs professional with extensive experience in the medical device industry. Currently serving as Principal Regulatory Affairs Specialist at Imperative Care Vascular since August 2022, Vida focuses on regulatory strategies and submissions for mechanical thrombectomy products. Prior roles include Regulatory Affairs Manager at V-Wave, where responsibilities included ensuring compliance with EU MDD and transitioning to EU MDR, and Senior Regulatory Affairs Specialist at Boston Scientific, leading regulatory activities for Class III medical devices. Experience also encompasses positions at Medtronic, where regulatory strategies for aortic products were developed, and as a Clinical Research Coordinator at the University of Florida, obtaining FDA approval for investigational devices. Vida began a career in quality assurance with a focus on compliance in pharmaceuticals and holds a BA in Biology from Brown University.