Xiaocong Guo

Xiaocong Guo, MS, RAC-Drugs, is an experienced Regulatory Affairs Manager with a focus on global clinical trial applications, currently working at Xenon Pharmaceuticals Inc. since March 2022. Prior experience includes roles at Lundbeck and Sandoz Canada, where responsibilities encompassed regulatory submissions, liaising with Health Authorities, and managing interactions with Health Canada. Xiaocong also held positions at Sivem Pharmaceuticals ULC and Pfizer Pharmaceuticals, contributing to regulatory documentation and workflow improvements. Educational qualifications include a Master's degree in Pharmaceutical Sciences and a Specialized Graduate Diploma in Drug Development (Regulatory Affairs) from Université de Montréal, as well as a Bachelor's degree in Food Science and Engineering from Jilin University.