Kobridge is a leading medical device consulting firm that specializes in regulatory affairs and quality system services. With a strong focus on assisting medical device companies, Kobridge offers expert guidance and support in navigating global market submissions. Their team of professionals is well-versed in various technical competencies, including CE marking, FDA regulations, MDSAP, and the handling of both active and non-active devices, combination devices, and animal origin devices.

Founded by Nicolas Clary, Kobridge has been serving medical device manufacturers since 2007. With extensive experience in the industry, Nicolas understands the challenges and complexities faced by his clients. He personally oversees the consulting processes and ensures that the unique needs of each client are met. To stay up-to-date with medical device regulations, clients can subscribe to Kobridge's newsletter.

Operating from two locations, Kobridge has offices in Seoul, Korea, and Lausanne, Switzerland. Whether you need assistance with regulatory affairs or quality system management, Kobridge is dedicated to providing effective solutions that bring relief and peace of mind to their valued clients. Contact them today to see how they can help your medical device business thrive.