Mengxin

Mengxin Ma is a professional in regulatory affairs with extensive experience in the pharmaceutical industry. Currently serving as Manager of Regulatory Affairs CMC at Regeneron since January 2023, Mengxin provides CMC regulatory support for gene therapy product development. Prior roles include Senior Regulatory Affairs Specialist and Regulatory Affairs Associate at A&Z Pharmaceutical from August 2018 to November 2018, where responsibilities included preparing FDA filings and conducting regulatory research for multiple markets. At Epic Pharma, from December 2018 to March 2020, Mengxin held positions as Senior Regulatory Affairs Associate and Associate Manager, managing high-quality submissions and ensuring compliance with FDA guidelines. Earlier experience includes internships at GSK and InvaGen Pharmaceuticals, focused on quality control and analytical testing.