Training Features

China Medical Device Regulations: Framework and Approval Process

This training guides you through the structure of China’s regulatory system, the key authorities involved in medical device registration, and the step-by-step process of obtaining approval for medical devices.
Format

E-Learning

Level

Basic

Trainer

Stephanie Huang

Exam

Exam and certificate included

Duration

1 hour
7 modules

Price

€ 200 or equivalent currency

Comprehensive Regulatory Expertise

Expand your global regulatory expertise by understanding China’s medical device regulatory framework and approval requirements. Strengthening your knowledge of international regulations supports more effective regulatory planning and successful market access strategies.
Upon successful completion of the program, participants receive a recognized certification, boosting their career prospects and demonstrating their expertise to employers and clients.

Certification and Career Advancement

We offer a flexible learning schedule, allowing professionals to balance their training with their busy work and personal lives, ensuring accessibility to a wide range of learners.

Flexible Learning Schedule

Modules

Explore the training modules available in this course

Meet the Trainer

Stephanie Huang

Stephanie Huang is the General Manager & Principal Consultant of Qserve Group China, where she develops regulatory strategies, conducts gap analyses, and fosters east-west connections, with a focus on NMPA compliance in the medical device industry; she holds an MCom from the University of Sydney and has experience in China, the UK, and Australia.