China Medical Device Regulations – A Comprehensive Overview

On-Demand

Course Overview

This course provides a comprehensive overview of China's medical device regulatory framework, including both pre-market and post-market requirements. China’s medical device regulations have evolved rapidly over the past two decades. This two-hour course covers the changes and key aspects of the regulations relevant to manufacturers wanting to market and sell in China.

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Additional Recommended Courses

Medical Device Single Audit Program (MDSAP)

This virtual instructor-led one-day course (delivered over 2 half days) covers the rationale for developing the Medical Device Single Audit Program (MDSAP), who the participating regulatory authorities are, and the specific audit criteria (including country-specific requirements) used during MDSAP audits.

This course discusses, in depth, the audit approach used by recognized MDSAP auditing organizations (AOs) as well as the MDSAP nonconformity grading system. Learners will also identify what MDSAP audit findings may trigger action from a participating regulatory authority.

This course pairs well as a prerequisite to MDSAP Internal Auditor Training (2 day).

Ask about our discount pricing when bundling courses together. We can also bring this course to your individual organization through virtual instructor-led or face-to-face training.

By the end of this training you should be able to:

Discuss the Medical Device Single Audit Program (MDSAP)
Evaluate the MDSAP Quality Management System (QMS) audit nonconformity grading system and recognize grades that may trigger regulatory follow-up
Identify the IMDRF MDSAP requirements and documents in use
Explain the MDSAP Audit Approach

Price: $800.00

Virtual Classroom Training