Lunch and Learn with Georgia Manufacturing Extension Partnership
In the early days of a medical device startup, it’s easy to focus solely on building the tech. But overlooking regulatory strategy, quality systems, and compliance can cause major delays and funding challenges later on.
Getting ahead of these requirements early is key to successful commercialization.
We'll cover questions like:
Which regulatory pathway fits your device?
How do design changes affect classification?
When should formal quality systems be in place?
Sarah Jo Tucker, Medical Device Industry Manager at GaMEP, along with Project Managers Sanjana Singh and Rebecca Stoneciper, will break it all down during a high-impact lunch and learn!
RSVP Required. Limited seating available.
📆 Date: April 29, 2025
🕐 Time: Doors open at11:30 AM | Presentation 12:00 PM - 1:00 PM
