Sarah Todeschini

Background

About Sarah Todeschini

As an accomplished QARA professional, I bring extensive expertise in navigating complex medical device regulations across North America and Europe, with proven experience handling medical devices from Class IIa to Class With a strong track record of successfully managing CE certifications and 510(k) submissions, I am deeply committed to ensuring compliance, product safety, and quality assurance at every stage of the regulatory lifecycle.I thrive in high-pressure environments, where my organizational and leadership skills enable me to seamlessly manage multiple complex projects. My proactive approach to regulatory strategy, coupled with hands-on experience in implementing and improving Quality Management Systems has resulted in successful audits and strengthened compliance frameworks.Having worked in startup and multinational organizations in both North America and Europe, I offer a unique perspective on regulatory challenges, providing innovative solutions tailored to specific business needs. As a collaborative team leader, I excel at fostering cross-functional relationships while being equally comfortable driving initiatives autonomously to achieve strategic goals.Passionate about regulatory excellence and product efficacy, I am dedicated to helping companies navigate evolving global regulatory landscapes while ensuring the highest standards in medical device safety and quality.Let’s connect if you want to discuss with a results-driven QARA leader with expertise in Class IIa to medical devices, offering strategic regulatory guidance and operational excellence.