David Pollard is an accomplished biomedical engineer and the current Associate Director of Regulatory Affairs at MCRA, an IQVIA business. With a strong background in scientific research, product development, and regulatory affairs, they focus on spinal and cardiovascular devices, tissue engineering, and regenerative medicine. Previously, David garnered extensive experience as a Regulatory Affairs Specialist and Associate at Zimmer Biomet, where they handled FDA submissions and supported international product registrations. They also contributed as a Biofabrication Research Assistant at the Medical University of South Carolina, developing innovative bioprinting methods. David holds a Master of Science in Bioengineering from Clemson University and a Bachelor's Degree in Biomedical Engineering from the University of South Carolina.
Location
Denver, United States