Webinar Features
Medical Device Registration in Asia-Pacific countries China and Singapore
Understand the regulatory pathways for market access, crucial for informed decision-making and compliance in China and Singapore.
Format
On-Demand Webinar
Level
Basic
Trainer
Stephanie Huang and Dennis Sarwin
Exam
Certificate of Participation included
Duration
1 hour
Price
Free
Comprehensive Regulatory Expertise
Watch this On-Demand webinar to learn more about the regulatory framework in Asia-Pacific countries China and Singapore, presented by our regulatory affairs associates around the world.
Watch on-demand webinars at your convenience, allowing you to fit learning into your schedule without missing essential information.
Flexible Viewing
Gain insights from industry experts and stay updated on the latest trends and regulations without the need to attend live sessions.
Access to Expertise
Meet the Trainer
Stephanie Huang
Stephanie Huang is the General Manager and Principal Consultant of Qserve Group China, specializing in China NMPA compliance and regulatory strategy development, with extensive experience in the medical device industry across China, the UK, and Australia.
Meet the Trainer
Dennis Sarwin
Dennis Sarwin joined Qserve in May 2022 as a Regulatory Affairs Associate, based in Arnhem, NL, bringing experience from medical device companies and expertise in global registrations, ISO 13485, and medical device development, backed by a Double Master of Science degree in Integrated Product Design and Biomedical Engineering from TU Delft.
