Christina Boydston

As a seasoned Regulatory Affairs Executive, I bring a wealth of experience across diverse medical device categories. My passion lies in driving cultural change, managing turnaround situations, and transforming regulatory functions from reactive to proactive postures. I excel in process improvement, tackling complex problems, and fostering cross-functional collaboration.
Throughout my career, I've developed a reputation for maintaining a calm demeanor in high-pressure environments. This has been crucial in my role as a subject matter expert in submissions, compliance management, and stakeholder engagement. I've successfully led teams of 25+ professionals, honing my people management skills and earning recognition as an exceptional communicator who can articulate and drive vision.
My track record includes implementing robust auditing processes and supporting new product development, resulting in zero external audit findings from notified bodies, FDA, and various regulatory agencies during my tenure at Zimmer Biomet. One of my proudest achievements was securing 510(k) clearance for a complex infusion pump system at BD - a feat that had eluded the company for five years prior.
I thrive on challenges and am committed to supporting growth in organizations. My goal is to continue leveraging my expertise to drive regulatory excellence and contribute to the advancement of medical device innovation.