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

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.