Jarvis Wu
Jarvis Wu is a regulatory affairs and quality assurance consultant with over five years of industry experience spanning medical device manufacturing and photovoltaic research.
About Jarvis Wu
He specializes in FDA 510(k) submissions, ISO 13485 quality management systems, and manufacturing engineering. He has led more than 30 successful 510(k) submissions across diverse medical device categories, showcasing technical leadership in navigating complex approval processes. Leveraging AI-driven tools, he streamlines regulatory workflows, improving documentation accuracy and accelerating the delivery of medical technologies to market. This approach enhances compliance efficiency and supports public health by expediting the approval of safe medical innovations. Trilingual in English, Mandarin, and Cantonese, Jarvis communicates effectively with international clients and regulatory authorities.
Prior to joining Pure Global, Jarvis held engineering and research roles at Providence Enterprise Limited and the Chinese Academic of Sciences. He holds two engineering degrees in STEM major from Arizona State University.