The JMDR strengthens its Asia Pacific regulatory expertise with appointment of Jack Wong to its Editorial Board
The Journal of Medical Device Regulation (JMDR) is pleased to announce the appointment of Jack Wong, Founder of the Asia Regulatory Professionals Association (ARPA), to its Editorial Advisory Board.
With more than 26 years’ experience across the pharmaceutical and medtech sectors, Jack brings extensive regulatory affairs expertise and a strong Asia Pacific perspective to the JMDR’s international RA community.
Jack founded the ARPA to support regulatory education and professional development across Asia. Now with more than 9,000 members, the ARPA brings together regulatory professionals, industry, academia and other stakeholders, helping to build regulatory knowledge and capability across the region.
Jack has also served as an adjunct professor or lecturer at institutions including The Chinese University of Hong Kong, Hong Kong University, the National University of Singapore and Tohoku University in Japan. He is also CEO of RNAscence, a biotechnology start-up supported by the Nanyang Technological University and the National Skin Centre in Singapore, and is involved in initiatives focused on health AI and connecting students with start-ups.
His expertise in regulatory strategy and the evolving medtech and healthcare landscape is regularly sought by industry and professional organisations. He serves on the Singapore Steering Committee of the Drug Information Association and contributes to discussions on regulatory developments across the Asia Pacific region, including medical device regulation, digital health and innovative regulatory pathways.
Jack’s appointment further strengthens the JMDR’s international editorial network and its commitment to providing regulatory professionals with authoritative, practical and globally relevant information on medical device regulation.
About the Journal of Medical Device Regulation
The Journal of Medical Device Regulation (JMDR), published by Global Regulatory Press, provides regulatory intelligence and analysis for professionals working in the global medical device industry. Through expert articles, in-depth analyses, regulatory news and podcasts, the JMDR helps manufacturers, regulatory affairs professionals and other industry stakeholders understand regulatory developments and their implications for market access and compliance.
For more information on the Journal of Medical Device Regulation, please contact Marija Capek
(tel: +44 7916 443811; email: sales@globalregulatorypress.com) or visit GlobalRegulatoryPress.com.
