ACIST Medical Systems
Linda Busklein is a seasoned professional in regulatory affairs and quality management, currently serving as Sr. Principal Regulatory Affairs Specialist at ACIST Medical Systems since March 2022. Prior to this role, Linda held significant positions at Reprise Biomedical, including Sr. Director of Quality and Regulatory Affairs, and Director of Regulatory Affairs. Additional experience includes roles at RTI Surgical® as Principal Regulatory Affairs Specialist and at Boston Scientific as Sr. Regulatory Affairs Specialist. Early career highlights include leading economic development initiatives in rural Norway as Daglig leder at Frosta Utvikling, and serving as Regulatory Affairs Manager at Vascular Solutions. Linda's educational background includes an MBA in finance and strategic planning from the University of St. Thomas and a BS in Chemistry from South Dakota Mines.
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ACIST Medical Systems
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ACIST Medical Systems, Inc. is a pioneering interventional and diagnostic technology company with a portfolio of advanced products, including the world’s first Rapid Exchange FFR and High Definition IVUS systems. It is also a global market leader in advanced contrast imaging systems for cardiovascular angiography and radiology imaging. Through these products, ACIST is demonstrating its commitment to bringing unique and innovative technologies that simplify cardiovascular procedures and empower clinicians to treat patients with superior care. As part of the Bracco Group, ACIST benefits from the resources of a multinational conglomerate with broad expertise in cath lab technology and a dedication to continuous advancement. Headquartered in Eden Prairie, Minnesota, USA, ACIST has worldwide presence with over 300 direct employees and facilities in Silicon Valley, Maastricht, Shanghai and Tokyo.