Evelyn Kok

Evelyn Kok is a Regulatory Affairs Specialist with extensive experience in regulatory compliance and quality assurance in the medical device industry. Currently employed at Arthrex since February 2024, Evelyn focuses on regulatory affairs in the Southeast Asia region. Previously, at Biofourmis from October 2022 to February 2024, responsibilities included preparing technical dossiers for Software as a Medical Device (SaMD) registrations and communicating with stakeholders on regulatory matters. Earlier roles include serving as a Regulatory Engineer at HEMO BIOENGINEERING LTD, where Evelyn prepared Class III medical device product dossiers and led a project team, and as a Regulatory Affairs and Quality Assurance Intern at Bioptimal International. Evelyn holds a degree in Biological Sciences from Nanyang Technological University Singapore, completed in 2021.