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Guidance on Medical Device Adverse Event Monitoring Scope

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Create Date September 20, 2018
Last Updated January 30, 2023

Guidance on Medical Device Adverse Event Monitoring Scope

Attached Files

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Decree 1 Annex 3 Guideline on Medical Device Adverse Event Monitoring Scope draft

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