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  4. Eurping, along with GMP Laboratory Glass...

Eurping, along with GMP Laboratory Glassware Washer, is due to appear at the second bio-pharmaceutical technology Industrialization Summit in 2020

       On October 15, the second Bio-pharmaceutical Technology Industrialization Summit Forum in 2020 was held in Suzhou. The conference invited mainstream CMO/CDMO enterprises, new technology suppliers of industrial processes, equipment, new technology suppliers of quality testing, representatives of mainstream manufacturers, etc., to build a comprehensive bio-pharmaceutical industry chain technology exchange platform.

       As a leading brand in the field of laboratory cleaning, Tianjin Eurping Instrument Technology Co., Ltd. was invited to attend the conference.



       In 2020, with the arrival of the post-epidemic era, the biomedicine industry has entered a period of rapid development. From the burgeoning antibody drugs such as monoclonal antibody and double antibody, to the much-heralded COVID-19 vaccine, to the hot cell and gene therapy drugs, the biomedicine industry has gone against the trend and become the main vanguard at the beginning of the era. According to the data, there are more than 2,200 kinds of biotechnological drugs in the development of the world at present, among which more than 1,700 have entered clinical trials, and the wave of biodrug industrialization has been roaring to come.
       In biological experiment laboratory will produce a large number of high concentration of nutrient solution containing toxic and harmful substances, such as culture medium, especially as in the present new vaccine development process, such as pollutant without timely cleaning, sterilization will cause serious consequences, experiment if personal safety protection measures to contain loopholes, the harm of experiment personnel can be fatal.
Eurping saw such problems as the difficulty of cleaning laboratory utensils, the lack of guarantee of cleanliness, and the great harm to experimenters, and launched an overall cleaning solution in the pharmaceutical field. Basic Q720 inside the appearance of the conference can clean the laboratory used all vessels, such as volumetric flask, triangle bottle and flask, tube, cylinder, a beaker, small sample bottles, especially the biological laboratory use petri dishes, one can wash 180, accord with ISO15883, 93 ℃ hot poison, plus ultraviolet disinfection function, double sterilization system, comprehensive security experiment safety and health.






       In the process of biological drug production, it is also very easy to cause waste pollution and biological bacteria pollution caused by improper cleaning, such as blood, culture medium, and various irregular pipelines.
In the case of vaccine production, the preparation, filtration, transfer, filling and other processes of vaccine production, the environmental cleanliness level must be A level operating in the context of B level. What does A level of cleanliness mean? No bacteria allowed! No more than 20 dust particles ≥0.5 m per cubic meter of air! This is a very stringent standard, and there are environmental monitoring online monitoring alarm facilities, to ensure that monitoring is always available. Under such strict production conditions, manual cleaning is difficult to control all the cleaning parameters, inconsistent cleaning and flushing effects, difficult to document, and not approved by FDA. Under such circumstances, industrial automatic cleaning system is the most convenient and safe cleaning method.




       Eurping GMP cleaning system Poseidon I product features

       Control system -- Siemens PLC SF-1200;

       Circulating system -- total circulating capacity of circulating pump 1600L/min; Pump casing impeller smoothness Ra≤0.6um;

       Pipeline system -- pressure monitoring of circulation pipeline and speed monitoring of spray arm;

       Drying system - double compression fan, hot air injection drying;

       Cleaning verification - four levels of authority management, provide USB data interface, can save and print cleaning data for audit tracking.



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