Practice on the data normalization of medical device adverse event reporting and exploration on improving the quality of the reports.
- Author:
Ling WANG
1
;
Jingxin ZHOU
;
Xuening ZHANG
;
Xudong LIN
Author Information
1. National Center for ADR Monitoring, Beijing. wangling@cdr.gov.cn
- Publication Type:Journal Article
- MeSH:
Databases, Factual;
Equipment and Supplies;
adverse effects;
standards;
Quality Control
- From:
Chinese Journal of Medical Instrumentation
2014;38(5):364-367
- CountryChina
- Language:Chinese
-
Abstract:
On the basis of real working practices in data normalization, the case reports from the monitoring system were studied, non-standard reports were summarized and the reasons were analyzed, the methods of data normalization and improving the reporting quality were discussed. The standard databases and the rule databases were created, they were capable of automatic completion of the standardization work of new cases.
