Pharmaceutical products are highly regulated commodities, and at all levels of sale/use packaging, identification and coding play a vital role in ensuring consumer safety and brand protection. If there is no clear and easy-to-read information and data, it is impossible to ensure compliance with laws and regulations, the safety of users, and supply chain backtracking […]
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
Challenges and Countermeasures of CIP Clean Design Read More »
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
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