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One-time use of infusion device adverse reaction analysis will be held in Changzhou
PubDate：2017-04-10Author：Sources：Views：1932
In 2014, the State Food and Drug Administration in recent years, the infusion of adverse events reported project study, the results show that individual infusion enterprises product design, material selection, process control, packaging, there are certain quality problems, such as enterprises ignored the The control of the additives in the material. Polymer branch to help enterprises improve product quality, from the production process, technically find the cause of the problem, in July 5, 2015 in Changzhou held a one-time use of infusion device adverse reaction analysis meeting.
Testing agency representatives, industry experts, clinical experts, business technicians, accessories business representatives attended a total of 87 people.
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