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Guidance on Medical Device Adverse Event Monitoring

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Create Date September 20, 2018
Last Updated February 7, 2023

Guidance on Medical Device Adverse Event Monitoring

Attached Files

File	Action
Decree 1 Annex 1 Guideline on Medical Device Adverse Event Monitoring draft	Download

NMPA (CFDA) Regulations, Post Market Surveillance (AE, Recall, etc.)