Kathryn Stager brings over 15 years of experience in the medical device industry and presently leads SPR’s Regulatory Affairs, Quality Assurance, New Product Development and Compliance functions. With a passion to always put the best interests of patients first, Kathryn has established the company’s Compliance Program and ISO 13485-certified Quality Management System. Kathryn has obtained numerous regulatory approvals for SPR’s clinical studies and products, and holds a US Regulatory Affairs Certification.
Prior to joining SPR, Kathryn worked at NDI Medical, supporting clinical studies and regulatory approvals for a neurostimulation technology designed to treat multiple urological indications that was ultimately acquired by Medtronic. Kathryn holds a master’s degree in bioengineering from the University of Pittsburgh and a bachelor’s degree in physics from Miami University (OH).