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When it comes to tablet coating machine, many manufacturers in the pharmaceutical and food industries will focus on the following two points: First, the equipment should be as flexible as possible to adapt to batch changes in order to respond quickly and flexibly to the changes of...

Fluid bed granulation, also known as one-step granulation, is a method in which the three steps of mixing, granulation and drying of conventional wet granulation are completed in a closed container at one time. In 1959, Dr. Wurster from Wisconsin, USA first proposed fluid bed granulation...

At present, with China’s GMP regulations in line with international standards, the level of drug production quality management has been greatly improved. However, it needs to be clearly recognized that in the process of implementing GMP, there are still many problems, such as...

One thing you should know about an automatic tablet press machine is that you cannot understand what it does without basic knowledge. I will take you through it and help you make a suitable choice at a convenient store, Seneeir, whose vast skills, information, and tools will serve...

At present, with China’s GMP regulations in line with international standards, the level of drug production quality management has been greatly improved. However, it needs to be clearly recognized that in the process of implementing GMP, there are still many problems, such as...

The granulation process refers to the adhesion of powders or fine particles to each other to produce large multi-particulate entities or particles. The dry granulation process usually refers to the granulation process that does not need to add liquid in the granulation process. During...

  With the expansion of Chinese APIs in the United States, Europe, Japan and other international markets, API manufacturers and R&D companies have increased the research and development of new drugs and generic drugs. After laboratory trials to large-scale production, large-scale...

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...

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...

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%...