Training Features
China Medical Device Regulations: Clinical Evaluation Requirements
This training provides an in-depth overview of the clinical evaluation requirements for medical devices in China, focusing on regulatory guidelines, data appraisal, and compliance processes.
Format
E-Learning
Level
Basic
Trainer
Stephanie Huang
Exam
Exam and certificate included
Duration
1 hour
6 modules
Price
€ 200 or equivalent currency
Comprehensive Regulatory Expertise
In 5 modules, learn about the the clinical evaluation requirements for medical devices in China, focusing on regulatory guidelines, data appraisal, and compliance processes.

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
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.