
Join us for an insightful session with Sarah Jo Tucker, an expert in medical device development and Industry Manager at Georgia Tech’s Georgia Manufacturing Extension Partnership (GaMEP). With over 8 years of experience spanning startups, academia, and industry, Sarah Jo leads GaMEP’s enhanced services designed to support medical device companies at every stage—from concept to commercialization.
In this session, attendees will:
- Explore GaMEP’s expanded capabilities in product development, regulatory strategy, and quality management systems (including ISO 13485).
- Learn how GaMEP partners with startups, manufacturers, and research teams to streamline development, ensure compliance, and reduce time to market.
- Gain actionable insights into overcoming regulatory and operational challenges with expert support tailored to the unique demands of the medical device field.
Who should attend?
Manufacturers, academic researchers, startup teams, and professionals in regulatory affairs, quality assurance, and product development who are 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.