The Technical Support Scheme for NMPA-registered medical devices in China typically includes:

1. Post-Market Surveillance: Ongoing monitoring of device performance and safety, including reporting adverse events and conducting periodic inspections.
2. Technical Documentation Updates: Regular updates to technical files and risk management documentation to reflect any changes in the device or its use.
3. User Training: Providing training and support to users to ensure proper handling and operation of the device.
4. Regulatory Compliance: Ensuring continued compliance with Chinese regulations and standards, including updates to relevant laws and guidelines.
5. Customer Support: Offering technical support for troubleshooting, maintenance, and handling customer inquiries.

Maintaining robust support is essential for ensuring continued compliance and addressing any issues that arise during the device’s lifecycle.

Contact Us：

Whatsapp or Wechat：+86 15816864648；email address：hito.lin@grzan.cn