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In this article, we will continue to share the DoE considerations for the selection and design of the R&D high shear wet granulator.   High Shear Granulator   Pilot research is the beginning of the life cycle of a drug. Senieer always stands on the user’s point...

  Wet granulation is a commonly used granulation process for oral solid preparations, and the core process equipment is a wet mixing granulator. From the design of the mixing paddle and cutter of the granulator, we explore its impact on the performance of the equipment.  ...

Difference Between GMP And cGMP   As we all know, China is currently implementing the GMP standard, which is a GMP standard formulated by the WHO and applicable to developing countries. It focuses on the requirements for hardware production such as equipment production. The GMP...

In 2021, the United Nations Climate Change Conference (COP26) was held in Glasgow, UK. At the end of the conference, the World Health Organization released a report which estimated that 9 out of 10 people in the world are affected by severe air pollution and asthma.    ...

For cleaning verification, what is important is Pharmaceutical Plant Equipment Cleaning Procedure, which is a major premise. Cleaning procedures are necessary before performing cleaning verification. Cleaning verification is to prove the applicability of the cleaning methods specified...

In the short term, the new coronavirus vaccine has accelerated to sea, pharmaceutical equipment continues to be in short supply, and Sinopharm and Kexing new coronavirus vaccine have been certified by WHO. In June, Kexing new coronavirus vaccine was granted emergency use certification...

To achieve a perfect “wet granulation process”, it also called  “rapid mixer granulator process”.  it must be based on the control of various parameters. This article will outline the many points that companies need to consider when designing or optimize a wet granulation...

At present, due to the increasing variety of products of various pharmaceutical companies, the factors affecting the quality of drugs in the production process are also increasing. Therefore, it is necessary for pharmaceutical companies to establish a sound quality management system...

Clean Room Commissioning Solution   The clean room commissioning stage belongs to the completion commissioning; our implementation is carried out in the empty state and static state, and the service items are provided: total air volume measurement, air volume balance, pressure...

With the continuous improvement of people’s requirements for drug safety, the national drug regulatory department is also increasing the supervision of pharmaceutical companies. In order to adapt to the rapid development of the pharmaceutical industry, it is particularly critical...