The MedTech global regulatory landscape is evolving. What is the future of the medical device industry—and is your organization ready?
Regulatory and product development departments need to do more than cooperate—they need to work hand in hand. Hosted by Sterling Director of Regulatory and Clinical Affairs Carrie Hetrick, with other leading industry experts, this on-demand MedTech webinar offers best practices to help your team produce synergistic results.
Learn how a robust regulatory strategy can help you:
The session is part of the digital MedTech conference, Global MedTech Regulatory Trends: True Quality Summit Series, presented by Greenlight Guru.
Watch How Regulatory Changes Can Impact Product Development now.
February 18, 2021
September 8, 2020