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Join us for an engaging session led by Sarah Jo Tucker, Industry Manager at Georgia Tech’s Georgia Manufacturing Extension Partnership (GaMEP) and a seasoned expert in medical device development. With over eight years of cross-sector experience in startups, academia, and industry, Sarah Jo now spearheads GaMEP’s expanded services tailored to support medical device innovators from concept through commercialization.
 
In this session, attendees will:

• Discover GaMEP’s enhanced capabilities in product development, regulatory strategy, and quality management systems, including expertise in ISO 13485.
• Learn how GaMEP collaborates with startups, manufacturers, and research teams to streamline development processes, ensure regulatory compliance, and accelerate time to market.
• Gain practical insights into navigating the challenges of the medical device lifecycle with expert guidance and customized support.

Who should attend?

Manufacturers, academic researchers, startup teams, and professionals in regulatory affairs, quality assurance, and product development involved in bringing medical devices to market.
 
Walk away with a clear understanding of how GaMEP can help you build smarter, scale faster, and navigate regulatory pathways with greater confidence.