Cisema will be participating in Medtech Canada’s Virtual Regulatory Medtech Conference 2021 that will take place on June 2 & 9 and October 20 & 21, 2021.
During the On-Demand Session, Cisema‘s regulatory experts will present the regulatory framework in China for digital health products. The regulation is rapidly evolving as it tracks the fast-moving techhnology changes. Key digital health trends will be discussed including telehealth, internet hospitals and AI/ML products. How does risk class classification for the NMPA (former CFDA) work? Are there any fast-track regulatory pathways? What are the latest updates regarding digital health regulations?
Upon registration of the event, the recorded version of our webinar session will be available for registrants to watch at anytime. Also, our regulatory experts will answer your questions and better equip you to access China’s digital health market.
Canada’s Regulatory Medtech Conference 2021 – Preliminary Virtual Conference Agenda
Dates: June 2 & 9, 2021 and October 20 & 21, 2021
On-Demand Session Speakers:
Mr. Hamish King, Chief Operating Officer, Cisema (Hong Kong) Limited
Hamish King is a lawyer by training – admitted in Hong Kong and NSW, Australia – supporting companies with difficult regulatory affairs queries for China. Formerly with UK Magic Circle Firm Linklaters in Hong Kong, he has nearly 10 years’ experience in the legal and regulatory fields and has obtained the RAC and CFA qualifications. Regularly writing articles and speaking on China market access and regulatory pathways, he currently lives in Hong Kong and specializes in NMPA registration of medical devices. Hamish has a close interest in the regulatory implications of digital healthcare and AI applications.
Mr. Jacky Li, Sales and Marketing Manager, Cisema (Hong Kong) Limited
Jacky Li focuses on market updates of medical devices in China (including Hong Kong and the Greater Bay Area) and is the Cisema lead to support the Hong Kong and China regulatory affairs for Taiwan and Hong Kong customers.
Mr. Arthur Ng, North America Business Development Manager, Cisema (Hong Kong) Limited
Arthur Ng attended SUNY in the United States and worked for various companies for 30 years ensuring CPSC, OSHA, and ANSI requirements were met and UL, TUV, IEC and CE regulatory guidelines were strictly adhered to. Arthur currently assists medical devices in Canada and the US with a smooth and efficient registration process in China.
Contact Cisema if you would like to learn more.
