As is the case in most industries these days, there is a heavy regulatory component within medical device manufacturing. Effective regulatory change management and compliant response across a multiple-team operated company is challenging and requires heightened transparency and collaboration. Laurence (Larry) Sampson joins PI to discuss the two-part deployment of PLM and RM in remaining consistently compliant.
Sr Director Medical & Lifescience Industry Strategy, Siemens PLM
Laurence Sampson is an accomplished technical manager with over 20 years of medical device experience including high volume process and product development projects. Laurence is currently Senior Director Medical & Lifescience Industry Strategy, and holds a B.S. in Mechanical Engineering from Colorado State University, and a M.B.A. from the University of Denver.