Measuring the cleanliness of a cleanroom is the main parameter of cleanroom classification, and plays an important guiding role in the design, maintenance and use of a cleanroom. When the cleanline...

1. The difference between the applicable fields of industry cleanroom and biological cleanroom: Industry cleanroom is suitable for fine machinery industry, electronic industry (semiconductor, i...

The vial powder filling machine, also known as the vial powder filler or the vial powder dosing machine, is a precision machine used in the pharmaceutical industry for automated powder filling. ...

Introduction The penicillin group of antibiotics is one of the most commonly used medications worldwide. The production of these antibiotics requires the use of specialized equipment to ensure t...

With the rapid development of economy and society, especially scientific experiments and high-tech production processes represented by microelectronics, biotechnology, and high-precision machinery,...

Refrigeration schemes should be compared technically and economically based on cooling requirements (cooling consumption, cooling method, frozen water temperature, etc.), water source conditions in th...

1、Whole room purification The purification treatment method that uses the centralized purification air-conditioning system to create an environment with the same cleanliness in the entire roo...

Dry granulation is to directly make powder raw materials into granular products that meet user requirements. After granulation, the bulk density increases significantly, which can not only control ...

1. Reasons of equipment manufacturing Wet granulation: Add binder or wetting agent to the raw material powder to make soft material, sieve to make wet granules, dry the wet granules and then...

1. Reasonable design air purification system Reasonable design and establishment of clean workshops and effective management are very important in pharmaceutical production. Through the desig...

With the rapid development of modern industry, the technical content of its products is more complex. In order to adapt to more and more industries relying on the production and assembly of their o...

The cleanliness level applicable pharmaceutical production dosage form and process ClassA/ClassB 1) Filling of terminally sterilized large-volume injections (≥50 ml); 2) Non-t...