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Carrie Britton

Carrie Britton

Director of Regulatory and Clinical Affairs

Resource Director of Regulatory and Clinical Affairs Carrie Britton has over 20 years of experience in the medical device industry. Ms. Britton leads regulatory, clinical, and quality programs at Sterling, helping companies navigate challenges in product development while establishing appropriate clinical, regulatory, and compliance structures during each stage of development. A seasoned subject matter expert in taking new products from R&D to market, she has used her regulatory and clinical expertise to aide in hundreds of successful regulatory submissions and clinical trials in the U.S. and Europe. Ms. Britton has led numerous quality management and business process improvement and management measures. She is also experienced in leading early and late-stage cross-functional medical product development programs, directing activities and teams for all phases of design controls, and creating collaborative alliances. She holds a Master of Science in Advanced Biotechnology, Regulatory Science from Johns Hopkins University, and a Bachelor of Science in Biology from Pacific Lutheran University. She finds great reward in helping patients through ushering products to market.

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Resources

Woman using modern glucose monitor connected to laptop

June 6, 2023

First, Do No Harm: Ensuring Medical Device Connectivity Solutions are Safe and Secure

Digital health solutions, like wireless technology in healthcare and medical devices that use Wi-Fi, have, and will continue to transform healthcare. They enhance patient experiences, such as...
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5 Mistakes Medical Device Startups Make

February 18, 2021

5 Mistakes Medical Device Startups Make

Startups are the lifeblood of medical device innovation. Without universities researching ways to solve pressing healthcare problems or doctors with experience in a particular field who have an idea to develop a prototype medical device that could help patients, the future technologies needed to help save lives wouldn't happen. But the long, arduous road through the FDA submission process to get market approval can take a long time and cost a lot of money without help. Sterling Medical Devices has been helping startups through the FDA approval process since 1998 without ever having a submission rejected.
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people developing a product

November 23, 2020

Sterling Helps Print Parts Win Contract with City of New York for Production of Medical-Grade Nasal Swabs

Sterling Medical Devices performed design services for a Class III breathing pacemaker with Major Level of Concern software, intended for use by patients who have lost neurological control of respiration. This life-sustaining device is comprised of two main components: an internal passive receiver and an external controller....
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