Clement Cheong
Clement Cheong is a regulatory affairs professional with over 10 years of experience in medical devices. In his role at Pure Global, he oversees Southeast Asia, Bangladesh and Pakistan medical device registration, and assists with Technical Documentation File (TDF) preparation.
About Clement Cheong
Clement uses his experience to craft and implement comprehensive regulatory strategies across Southeast Asia/Bangladesh/Pakistan, and specializes in renal, hospital, and vascular devices.Prior to joining Pure Global, Cheong held regulatory positions at Nipro Asia and Oculus. He holds bachelor’s and master’s degrees in biomedical sciences from The National University of Singapore.
Latest Articles
Singapore’s Health Sciences Authority (HSA) is now a globally recognized reference agency, offering manufacturers a fast track into key Asia-Pacific markets. This article explains how HSA approval can streamline registration in Thailand, Australia, and Hong Kong, and how its WHO Stringent Regulatory Authority status boosts access for high-risk IVDs. Leveraging HSA can cut costs, reduce timelines, and accelerate international expansion.
With a population of 5+ million, Singapore has the highest GDP per capita in Asia, according to Trading Economics.