Chris Phillips

Christopher Phillips, MSHS, RAC, CMDA is a highly experienced professional in regulatory affairs and quality management within the medical device industry. With a background in bio-business management and biomedical engineering, Christopher has held various roles in leading companies such as Epitel, Fluidx Medical Technology, BD, CR Bard, and Vital Access. Christopher's expertise includes managing regulatory submissions, clinical investigations, quality systems, and global regulatory efforts for innovative medical devices. With a Master of Science in Health Science in Regulatory Affairs, Christopher has demonstrated strong leadership and strategic planning skills in navigating the complex intersection of regulatory and clinical affairs.