Shandong Medical Device Adverse Event Evaluation Platform Settled in Heze

Medical Network May 30th Recently, the provincial-level evaluation platform for medical device adverse event professional evaluation platform was held in Heze Municipal Hospital and Caoxian People's Hospital. Tian Yuejie, deputy director of Shandong Adverse Drug Reaction Monitoring Center, and Heze City Food and Drug Administration Deputy Director Director Zhao Heng, Xia Jiansheng, Deputy Dean of Heze Municipal Hospital, Yue Rongzheng, Chairman of Cao County People's Hospital, and relevant department directors attended the awarding ceremony.

province drug Adverse reactions Tian Yuejie, deputy director of the monitoring center fully affirmed that Heze has been in recent years. medical instruments The achievements made in safety monitoring have introduced the background of the establishment of the provincial professional evaluation platform and the important role that the platform will play after it is put into operation. It is suggested that the establishment of the platform should be the starting point for the promotion. hospital The overall optimization of the monitoring mechanism, efforts to build good experience, good practices. Zhao Heng, Deputy Director of Food and Drug Administration of Heze City, attended the awarding ceremony and put forward three requirements for platform operation and future monitoring work:

First, strengthen organizational leadership, establish a leading group for monitoring work, improve work systems and reporting procedures, provide support in terms of funds, equipment and facilities, fully evaluate the role of the baton, and integrate platform work as an important part of monitoring work into hospital assessments. ;

The second is to take the construction of the platform as an opportunity to strengthen collaboration, give full play to the role of the team of engineers and clinical experts, further tap the risk signals, and make achievements for the professional evaluation of Heze medical device adverse events;

Thirdly, the monitoring personnel must actively collect relevant data, truly fill in the questionnaires of the relevant key monitoring species, and report adverse event reports, cooperate with the supervisory agencies and monitoring agencies to do relevant research and analysis.

In the next step, Heze will take the provincial professional evaluation platform for medical device adverse events as an opportunity to focus on the monitoring of high-risk medical device types, constantly improve the level of special monitoring, enhance the ability to find risk signals, and strive to provide technical support for supervision.