亚洲欲妇xxxxx69丨在线免费激情视频丨成码无人av片在线电影网站丨强制高潮18xxxx按摩丨最新91在线丨日韩一区国产二区欧美三区丨麻豆秘密入口a毛片丨免费黄色毛片丨国产夫妇肉麻对白丨欧美在线三级艳情网站丨精品久久免费丨狠狠v欧美ⅴ日韩v亚洲v大胸丨欧美肥臀大乳一区二区免费视频丨乌鸦热v2ba在线观看丨免费a级片视频丨久久国产成人午夜av浪潮丨国产精品亚洲а∨天堂123bt丨又黄又爽又无遮挡免费的网站丨亚洲精品中文字幕乱码无线丨麻豆高清免费国产一区

Tel: 18052162330 | | 中文 | ENLISH
News
Your current location: Home News
Quality assurance of sterility test for medicinal glass bottles Release time: 2020-08-23 Visited: 2441 Times

The most important quality assurance of medical glass bottle depends on sterility test. In this regard, a good aseptic testing packaging is indispensable.


The risk of sterility test of medical glass bottles generally comes from the following contents:


1、 The following are the credibility of sterilization process; 2. The environmental pollution level of microbial strains of raw materials; 3. Whether a sound aseptic testing assurance system management has been formulated; 4. Whether a sound aseptic testing assurance system management has been formulated; 4;


Then, to ensure the sterility test of medical glass bottles, we must start from the following contents:


1. Effective sterilization methods should be selected, which can exceed the actual effect of complete sterilization. Generally speaking, ethylene oxide sterilization or cobalt 60 sterilization method should be used for sterilization. 2. To test the environmental pollution level of raw materials, generally speaking, the spread of microbial strains in solid raw materials will not be symmetrical, resulting in the test results may not necessarily mean the overall situation of the whole batch of raw materials. Relevant purchase specifications of raw and auxiliary materials should be formulated, and the relative microbial strain level should be required. 3. Select excellent processing technology to carry out manufacturing to ensure the excellent sealing performance of the bottle body, and select the matching cap with good sealing performance, so as to reasonably ensure the sealing. 4. Formulate and improve the aseptic testing system management to ensure that the environment of the production workshop and the relevant specifications of the purification workshop exceed the provisions of GMP and the company's own specifications.