JaeYeong is a senior consultant for UL Korea. she has over 8 years of regulatory compliance, quality assurance.
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JaeYeong provides consulting services for medical device manufacturers in the area of global medical device regulations, including MFDS registration, KGMP, FDA (such as 510(k) submission, etc.) and Risk Management. Before starting work at UL in 2013, JaeYeong was a technical file reviewer for the Korea MFDS for medical devices and before that, she was in Regulatory Affairs at Olympus Korea.