Senior Consultant, Quality and Regulatory Affairs (Asia Pacific)

JaeYeong Noh has over 10 years of industry experience, primarily focused on high-risk devices such as disposable medical materials and electrical products. Based in Seoul, South Korea, she is one of our key contacts for local MDR inquiries and also possesses in-depth experience with KGMP applications, including auditing for initial registration approvals, renewals, and modifications. JaeYeong held previous roles as a medical device technical reviewer at MFDS and RA positions at Olympus Korea. She has peer reviewed more than 100 regulatory filings and reports.