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1 Overview Of Cleaning Verification And Four Stages   In pharmaceutical enterprises, the same equipment may be used for the production of multiple products, and after the end of drug production, effective cleaning of the relevant equipment used in production is a necessary means...

As macromolecular drugs, biological products are relatively complex in structure and function, and their efficacy is mostly directly related to their biological activity. Due to the high-quality and active characteristics of biological products, most biological products cannot be...

The pharmaceutical industry has a wide range of equipment and performance – equipment management is particularly important to ensure that the pharmaceutical manufacturing process and quality of the drug comply with the requirements of Good Manufacturing Practice (GMP). For excellent...

Since the COVID-19 outbreak, the pressure on pharmaceutical companies to get their medicines to market faster has increased dramatically. To this end, pharmaceutical companies are now paying more and more attention to the digital transformation of drug production, hoping to4.0to simplify...

This paper introduces several sterilization methods of sterile drugs : humid heat sterilization, dry heat sterilization, radiation sterilization, ethylene oxide sterilization and sterilization filtration, studies the sterilization principle, influencing factors, advantages and disadvantages...

The application of biological clean rooms is becoming more and more extensive, and they are currently concentrated in hospital operating rooms and wards, pharmaceutical factories, biosafety laboratories, animal rooms, etc. The same level of clean room, due to different application...

1. About GMP Certification Hospitals, food, pharmaceuticals and other safety and health-related industries, from each process must be certified by the relevant national agencies to ensure that the quality of production meets the requirements of harmless to the human body. Taking medical...

In the process of tablet production, there are many factors that affect the quality of drugs, so it is necessary to supervise and control all aspects of drug production. Starting from the production process of tablets, this paper analyzes various quality control points in the production...

There are many theories and methods of modern equipment management, and the ABC classification management method is an effective scientific management method. In the production equipment management of Suzhou Luoli Technology Co., Ltd., the secondary ABC analysis method was successfully...

Teams of experts at pharmaceutical companies have always been keen to study continuous production: what aspects of this technology are mature? What other aspects still have problems? ——The pharmaceutical industry is facing the transformation of production mode, and continuous production...