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CFDI | Key Points Of Contamination Control Strategies For Sterile Drugs

Contamination control is one of the core contents of drug production quality management. Based on the basic requirements of drug production quality management, this paper summarizes the key points of sterile drug contamination control strategies; , equipment and components, facility environment, materials, process, detection and prevention, etc. to refine and explain the typical and easily […]

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New Technology | Quality Considerations Using Continuous Flow Chemistry In API Manufacturing

Continuous flow chemistry is a promising emerging pharmaceutical technology, which has the advantages of shortening the production cycle, high degree of automation, environmental friendliness, energy saving and emission reduction, etc. It is especially beneficial to reactions that are difficult to perform in batch mode. Active Pharmaceutical Ingredients, API) technology innovation trends. However, due to quality

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Discussion On The Application Of Low-Temperature Freeze-Drying Technology In The Production Of Powder Injections

Under the conditions of modern society, people begin to pay attention to the production and preparation process of medicines. In order to ensure the stability of drugs, relevant professionals have begun to develop important technologies for processing drugs, including freeze-drying technology. At present, most pharmaceutical companies use comprehensive drying technology, but there are still many

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