Kim Torluemke began her career in 3D printing by leading the development effort on Medical Modeling’s first FDA cleared 3d printed product in 2009. She continued on a path of increasing quality and regulatory oversight which, at its height, included oversight for 3D printed medical devices, dental products, and software as medical device produced across 5 sites on 3 continents. After ending her tenure with 3D Systems as their Vice President of Regulatory, she lent her expertise guiding clients through the evolving landscape of regulation to ensure safe and effective products make it efficiently to market. Currently she holds the title of Director, Regulatory Affairs and Quality, for Ricoh 3D for Healthcare, working to innovate and improve clinical outcomes and overall quality of life by enabling access to patient-matched medical solutions through an integrated infrastructure. Kim obtained a BS from the Colorado School of Mines in Mechanical Engineering, and holds a RAC US credential demonstrating thorough knowledge of regulatory functions throughout product lifecycle for medical devices, IVDs, Pharmaceuticals, and Biologics.