Christopher Phillips is an experienced leader in Medical Device Regulatory Affairs, Clinical Affairs and Quality Assurance. Christopher has helped bring innovative medical devices to market in the USA, Europe, Canada, Australia, Brazil and other global markets; and has built and maintained ISO 13485- and 21 CFR 820-compliant Quality Management Systems. Christopher has played key roles in designing, developing, and launching novel software-based medical devices, digital health software, implantable medical devices and disposable medical devices. Christopher also has broad experience gained throughout the medical device development and marketing process, from building business plans and gathering marketing input from key opinion leaders, to developing nonclinical and in vivo studies, to designing and supporting clinical trials and clinical evaluations, to training sales teams and clinicians on product use. Christopher possesses extensive knowledge and understanding of requirements of the FDA, European Medical Device Regulation and Medical Device Directive, Canadian Medical Devices Regulation, and other international regulations. Christopher completed a Master of Science degree in Regulatory Affairs and holds RAPS’ RAC (US) and ASQ’s CBA certifications.