少妇高潮后中文字幕_久色视频_日本天堂资源_久久在现视频_日本污ww视频网站_2021无码最新国产在线观看

Welcome to Shenzhen Zhongjing Global Purification Technology Co., Ltd.!

Shenzhen Zhongjing Global Purification Technology Co., Ltd.

24-hour service hotline:0755-29103270

Medical equipment GMP workshop
National service hotline0755-29103270

Diagnostic reagent GMP workshop

Author: Shenzhen Zhongjing Global Purification Technology Co., Ltd.Time:2018-07-26 11:18:42Views:2464

Diagnostic reagent GMP workshop
  • Diagnostic reagent GMP workshop

Medical devices are widely used in IVD to refer to products and services that obtain clinical diagnostic information by detecting tissues and secretions such as blood and other substances outside the human body. The “test” in the “test and inspection” commonly used in hospitals in China includes most subdivisions of IVD—such as 1 clinical chemistry, 2 immunoassay, 3 molecular diagnosis (MDx), and elemental diagnosis. , microbiological diagnosis, urine diagnosis, blood coagulation diagnosis, tissue diagnosis, hematology and flow cytometry. The first three categories are the mainstream IVD methods for medical institutions in China.


requirements

1. Enzyme-linked adsorption assay reagents, fluorescent reagents, luminescent reagents, polymerase chain reaction (PCR) reagents, gold standard reagents, dry chemical reagents, cell culture media, calibrators and controls, enzymes, antigens, antibodies, and Processes such as liquid preparation, coating, dispensing, filming, drying, cutting, filming, and inner packaging of other active components and at least 100,000 purification environments should be carried out. . The dispensing of sterile materials must be in the local level. The production of common chemical diagnostic reagents should be carried out in a clean environment.

2, YY 0033-2000 sterile medical device production management specifications; 2, YY / T 0567.1-2005 aseptic processing of medical products 3, YY / T 0567.2-2005 aseptic processing of medical products 4, GB 50457-2008 Pharmaceutical industry clean factory design specification

Third, the requirements of temperature and humidity 1, with the requirements of the production process. 2. When there is no special requirement in the production process, the clean room (area) with air cleanliness of 100,000 grades should be 18 °C ~ 26 °C, the relative humidity should be 45% ~ 65%; the air cleanliness is 100,000, thirty Class 10,000 clean room (zone) temperature should be 18 ° C ~ 26 ° C, relative humidity should be 45% ~ 65%. When there are special requirements, it should be determined according to the process requirements. 3. The temperature of the personnel purification room should be 16 °C ~ 20 °C in winter and 26 °C ~ 26 °C in summer. Including: partition wall, ceiling, floor, purification, air conditioning, fire protection, pure water pipeline, pressure difference.

Fourth, the test content: temperature and humidity, cleanliness, pressure difference, gas exchange times, sedimentation bacteria


Zhongjing Global is committed to the design and construction of the GMP workshop for medical device purification workshops, serving many second-class and three-category medical device companies.

Undertake: sales and installation of purification equipment across the country

Get quotes quickly

*The quotation will be sent to your mobile phone as a text message or contact a professional technician to contact you.

  • *
  • *
  • *
主站蜘蛛池模板: 久久精品熟女亚洲AV麻豆 | 日韩激情一区二区三区 | 一区二区三区韩国 | 九一免费网站 | 喷水高潮在线观看 | 97久久超碰国产精品 | 日本啪啪动态图 | 日韩视频1 | 男人桶女人18禁止网站 | 精品国产品国语在线不卡 | 欧美老熟妇乱XXXXX | 亚洲色噜噜噜噜噜噜国产 | 最新国产区 | 91精品国产乱码久久桃 | 亚洲色WWW永久网站 日日躁夜夜躁白天躁晚上 欧美最猛黑人xxxx黑人猛叫黄 | 女人自慰Aa大片 | 伊人狠狠干| 日韩高清国产一区在线观看 | 同性男男无遮挡无码视频 | 粉嫩一区二区三区粉嫩91 | 国产黄色网址在线看 | 囯产精品一品二区三区 | 丰满老熟女毛片 | 国内精品久久久久久影院 | 中文字字幕在线中 | 久久久久爽人综合网站 | 91华人在线观看 | 国产第一尤物在线观看 | 黑人干嫩模在线观看 | 国产成人精品一区在线播放 | 天堂а在线中文在线新版 | 污在线观看视频 | 国产草草影院 | 91精品国产人妻国产毛片在线 | 人人妻人人狠人人爽天天综合网 | 成人性视频免费 | 中文字幕丰满乱子伦无码专区 | 天堂视频一区二区 | 国产内射xxxxx在线 | 97色网| 一本一本久久a久久精品综合 |