Will Chen has over 25 years of experience in pharmaceutical product registration. He managed regulatory affairs at multinational corporations and CROs for more than 12 years, leading over 100 drug and medical device registration applications in China and the U.S., including pre-IND meeting requests, IND, NDA, and supplemental applications. Prior to that, he spent 13 years working in drug regulatory authorities, responsible for document review, on-site inspections, and drug testing.