Stephanie G. Garth

Stephanie Garth has 29 years of quality and regulatory experience in the medical device industry with 24 years particularly focused on the life science sector. She started with the FDA as support for the regional small business industry for drugs, medical devices, biologics, food, etc. and trained as a Consumer Safety Officer. After FDA, Stephanie has worked for medical device companies and IVD industry leaders to ensure quality, regulatory and risk management principles are deployed in the product’s design, good manufacturing practices and supply chain management. She has helped companies design, launch, manufacture & supply hundreds of IVD products around the globe. Stephanie has helped companies through consulting and direct employment over the course of her career. She is currently with The Binding Site as the VP of QA for North America.