admin@hepacleanroomfilter.com
Key Considerations for The Aseptic Production of Sterile Drugs in Isolators
2025-06-13 [ Industry News ]
I. Glossary Isolator A contained, decontaminated environment meeting Grade A/ISO 5 conditions used for aseptic process manufacturing that provides an uncompromised, continuous isolation of its interior from the external environment. Once de......
What Are the Items and Specification Requirements for Cleanroom Testing?
2025-05-16 [ Industry News ]
Q1：Cleanroom inspection for cleanliness check 1. A cleanroom is a room that controls the concentration of particles in the air. 2. When using them or during construction, the induction, generation and retention of particles in the room shou......
GMP Cleanroom Classification and Regulatory Focus Areas
2025-05-09 [ Industry News ]
In the pharmaceutical industry, a dust-free and clean environment is of vital importance for the production of pharmaceutical enterprises. Especially for products that require aseptic production, any contamination during the production proc......
Technical Analysis of Cleanroom LAF / Modular Clean Room
2025-04-11 [ Industry News ]
The cleanroom laminar flow hood LAF is composed of fan, HEPA filter, plenum, shell, pre-filter, damping layer and other components, which is a local vertical unidirectional flow purification equipment, because the unidirectional flow gas or......
Standard Construction Requirements for PCR Laboratories
2025-04-03 [ Industry News ]
PCR laboratories are mainly located in the laboratory and pathology department, which is characterized by a large increase in trace amounts of DNA. PCR is a conventional method for molecular biology research and experiments, and is applied ......
