The Bench2Market series, hosted by Biolocity at Georgia Tech, is offering an introductory session on regulatory strategy for medical devices. This session, named “FDA Regulatory Strategy: Regulatory Pathways Options and Timing,” is designed for entrepreneurs new to medical device regulatory affairs who want to learn about the regulatory requirements for bringing products to market. The session will be led by Grace Powers, who will cover essential topics including the definition of a medical device, device classification, pre-market submission types, and the steps for successfully launching a new product.

The session is part of the 2024-2025 Bench2Market series, which provides commercialization guidance to the university research community. The event will take place on April 30, 2025, at 12:00 PM and will be hosted via Zoom. Visit the registration page for the event here to learn more.