Linda Chan
About Linda Chan
Linda Chan is the Regulatory Affairs Lead at Bristol-Myers Squibb in Hong Kong, with over 15 years of experience in regulatory affairs and product management within the pharmaceutical industry.
Current Title
Linda Chan currently holds the position of Regulatory Affairs Lead at Bristol-Myers Squibb in Hong Kong. She has been in this role since 2018 and is responsible for navigating complex regulatory landscapes in the Asia Pacific region.
Previous Experience
Before joining Bristol-Myers Squibb, Linda Chan worked as a Regulatory Affairs Manager at Baxter International Inc. from 2015 to 2018. She also served as a Regulatory Affairs Pharmacist at Guerbet for a year between 2014 and 2015. Additionally, she held the position of Regulatory and Medical Affairs Manager at Sandoz from 2011 to 2014 and was a Product Manager at Novartis from 2008 to 2010.
Educational Background
Linda Chan earned her Bachelor of Pharmacy (BPharm) from The Chinese University of Hong Kong. She furthered her education by obtaining a Master of Business Administration (MBA) from The Hong Kong University of Science and Technology.
Industry Expertise
With over 15 years of experience in regulatory affairs and product management, Linda Chan has developed extensive knowledge in regulatory requirements and compliance for pharmaceutical products in Hong Kong and the broader Asia Pacific market. Her expertise is highlighted by a proven track record of successful product registrations and market authorizations across multiple countries in the region.
Industry Involvement
Linda Chan actively participates in industry forums and regulatory affairs conferences to stay updated on the latest regulatory changes and trends. Her involvement in these events ensures she remains at the forefront of the regulatory affairs field.