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Notice on issuing "Guide for Monitoring Medical Device Adverse Events (Trial)"SFDA [2011] No. 425
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- Time of issue:2018-07-10 16:53
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(Summary description)Noticeonissuing"GuideforMonitoringMedicalDeviceAdverseEvents(Trial)"SFDA[2011]No.425 FoodandDrugAdministrations(DrugAdministrations)ineachprovince,autonomousregionandmunicipality,andFoodandDrugAdmi
Notice on issuing "Guide for Monitoring Medical Device Adverse Events (Trial)"SFDA [2011] No. 425
(Summary description)Noticeonissuing"GuideforMonitoringMedicalDeviceAdverseEvents(Trial)"SFDA[2011]No.425 FoodandDrugAdministrations(DrugAdministrations)ineachprovince,autonomousregionandmunicipality,andFoodandDrugAdmi
- Categories:Industry News
- Author:
- Origin:
- Time of issue:2018-07-10 16:53
- Views:0
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Notice on issuing "Guide for Monitoring Medical Device Adverse Events (Trial)"SFDA [2011] No. 425
Food and Drug Administrations (Drug Administrations) in each province, autonomous region and municipality, and Food and Drug Administration of Xinjiang Production and Construction Corps:
In order to strengthen the monitoring of adverse events involving medical devices, based on the relevant provisions of the“Management Approaches for Reassessing and Monitoring Medical Device Adverse Events (Trial)”, the State Food and Drug Administration formulated the “Guide for Monitoring Medical Device Adverse Events (Trial)”, whose issuance is announced hereby. Please make references and executions thereto.
Attachment: Management Approaches for Reassessing and Monitoring Medical Device Adverse Events (Trial)
State Food and Drug AdministrationSeptember 16, 2011
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