As an Amazon Associate I earn from qualifying purchases.

This handbook covers medical device regulatory systems in different countries, ISO standards for medical devices, clinical trial and regulatory requirements, and documentation for application. It is the first to cover the medical device regulatory affairs in Asia. Experts from influential international regulatory bodies, including the US Food and Drug Administration (FDA), UK Medicines and Healthcare Products Regulatory Agency, Japan Pharmaceuticals and Medical Devices Agency, Saudi Food and Drug Authority, Korea Testing Laboratory, Taiwan FDA, World Health Organization, Asian Harmonization Working Party, Regulatory Affairs Professionals Society, and British Standards Institution, have contributed to the book. Government bodies, the medical device industry, academics, students, and general readers will find the book immensely useful for understanding the global regulatory environment and in their research and development projects. The updated fourth edition includes specific contributions that address the needs of startups. Amazon Key topics: About the Author: Jack Wong brings over 26 years of experience in the pharmaceutical and MedTech sectors as the founder of the Asia Regulatory Professionals Association (ARPA), which has more than 7,600 members, and as the CEO of RNAscence, a biotech startup that originated from Nanyang Technological University and the National Skin Centre in Singapore. He serves as an adjunct professor and lecturer at several prestigious institutions, including the Chinese University of Hong Kong, National University of Singapore, and Tohoku University in Japan. Raymond K. Y. Tong is professor and founding chair in the Department of Biomedical Engineering, the Chinese University of Hong Kong; chair, the Hong Kong Local Responsible Person Panel; chair, the ARPA Hong Kong Academy; and honorary advisor, the