Purified water should be transported by Syringe Printing Machine Manufacturers pipeline. The piping design should be simple and blind tubes and dead ends should be avoided. Pipes shall be made of stainless steel pipes or other pipes that have been verified to be non-toxic, corrosion-resistant and do not bleed out contaminated ions. The valve should be a hygienic valve with no dead angle, and the purified water should be marked to indicate the flow direction.
Pipes and conveying pumps for conveying purified water and water for injection should be cleaned, disinfected and sterilized regularly, and can be put into use after passing the verification.
With the development of China’s economy and the acceleration of globalization, Chinese pharmaceutical companies, especially large pharmaceutical companies, are facing unprecedented challenges.
machine
To enter the European market, products must be produced and certified according to cGMP regulations; products must enter the US market and be produced and certified according to the US Food and Drug Administration FDA regulations.
Due to the increasingly strict requirements of the market for production processes and product quality, pharmaceutical companies have been seeking to optimize production processes and standardize production processes; more and more pharmaceutical companies have realized that the introduction of information technology is to improve corporate management. Level * the right way.
Old production methods are difficult to adapt to new requirements
Development of GMP quality management system
Figure 1: Development of GMP Quality Management System
https://www.syringeassemblymachine.com/product/printing-machine-series/
Pipes and conveying pumps for conveying purified water and water for injection should be cleaned, disinfected and sterilized regularly, and can be put into use after passing the verification.
With the development of China’s economy and the acceleration of globalization, Chinese pharmaceutical companies, especially large pharmaceutical companies, are facing unprecedented challenges.
machine
To enter the European market, products must be produced and certified according to cGMP regulations; products must enter the US market and be produced and certified according to the US Food and Drug Administration FDA regulations.
Due to the increasingly strict requirements of the market for production processes and product quality, pharmaceutical companies have been seeking to optimize production processes and standardize production processes; more and more pharmaceutical companies have realized that the introduction of information technology is to improve corporate management. Level * the right way.
Old production methods are difficult to adapt to new requirements
Development of GMP quality management system
Figure 1: Development of GMP Quality Management System
https://www.syringeassemblymachine.com/product/printing-machine-series/
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