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Companies should focus on “the value of CIP cleanability design” – improving the cleaning performance of aseptic process components. This article will provide a fresh perspective for CFOs and those making capital expenditure decisions while also concerned with enterprise facility utilization, operating costs, and carbon emissions.   It is an indisputable fact that even in

The production workshop of the pharmaceutical factory is different from the general comfortable air-conditioned room. The indoor temperature and humidity control requires high precision. Generally, the temperature is required to be 22 °C ± 2 °C, the relative humidity is within 55% ± 5%, and the cleanliness of the air is required. There are also

Clean facilities are the basic conditions to ensure the product quality of pharmaceuticals, medical devices and packaging materials that directly contact medicines and the quality of pharmaceutical preparation in hospital preparation rooms, and to prevent product pollution from the production (preparation) environment. The production (preparation) area must meet the specified environment parameter standard. In order