About me
I received my Master’s degree in Pharmacology from National Yang-Ming University, Taiwan. I began my career at the Taiwan Food and Drug Administration (TFDA) through alternative military service, where I gained foundational experience in regulatory review. I later worked in the pharmaceutical industry as a Regulatory Affairs specialist, supporting NDA submissions. Currently, I serve as a Project Manager at the Center for Drug Evaluation (CDE), with over five years of experience managing regulatory review applications, including New Drug Applications (NDAs), Abbreviated New Drug Applications (ANDAs), and Investigational New Drug (IND) applications. My expertise focuses on regulatory science and pharmacology.
