Industry News

As industries across pharmaceuticals, electronics, and medical device manufacturing face growing demands for controlled environments, modular cleanrooms are emerging as a preferred solution. With fast installation, custom design flexibility, and material versatility, modular cleanrooms offer a future-ready alternative to traditional cleanroom construction. Unlike fixed-build structures, modular cleanrooms are assembled from prefabricated panels and components, enabling […]

Pharmacy clean rooms are controlled environments designed to maintain sterility and prevent contamination during the preparation of pharmaceutical products. Whether it’s sterile compounding or hazardous drug handling, pharmacy clean rooms play a vital role in protecting both patients and healthcare staff. In this blog, we’ll walk you through everything you need to know about pharmacy

In cleanroom management, personnel are both a critical resource and the greatest source of potential contamination. Studies show that even with advanced filtration systems and protective equipment, cleanroom integrity can be severely compromised if human behavior is not properly managed. Therefore, developing a clear, enforceable personnel behavior plan is key to ensuring consistent product quality

Modular cleanrooms offer a flexible and scalable solution for industries that require controlled environments. From pharmaceutical labs to electronics manufacturing, modular cleanrooms are designed for quick installation, easy expansion, and strict contamination control. This guide covers four popular types: Modular Cleanrooms, Modular Hardwall Cleanrooms, Softwall Cleanrooms, and USP-797 Cleanrooms. 1. Modular Cleanrooms Modular cleanrooms are

By: Cleanroom Requirements Expert in Biomedical Industry Q1: How do we determine the appropriate cleanroom classification for our biomedical product? A: Cleanroom classification depends on two main factors:1. Product type (e.g., sterile drug, cell therapy, medical device)2. Process risk level (e.g., open vs. closed system, exposure risk) For example:– Aseptic injectable drugs typically require ISO

When people hear “clean room,” they often assume it means a completely dust-free environment. So, does building a clean room mean your workshop will have zero dust? The answer is more complex. Although clean rooms are carefully designed and strictly managed to meet specific cleanliness standards—often reaching ISO Class 5 or 6—they can still generate

In modern industrial production, such as medicine, electronics, food and other industries, environmental control of clean rooms (dust-free rooms) is crucial. As an important supporting equipment for clean rooms, cargo shower rooms (cargo air shower rooms) are mainly used to efficiently remove dust from goods and materials entering the clean area to prevent external pollutants

As an indispensable special environment in the fields of precision manufacturing, pharmaceutical production, biotechnology and electronics industry, the performance testing of clean rooms is directly related to product quality and production safety. This article will introduce the core items of clean room testing in detail to help you fully understand the key content of clean

With the rapid development of industries such as 5G, artificial intelligence, and semiconductors, the requirements for the production environment of electronic component manufacturing are becoming increasingly stringent. Recently, a new Class 1,000 clean room for electronic components built by a certain technology company was officially put into use. The clean room strictly follows the ISO

Constant temperature and humidity clean rooms have many advantages, which make them indispensable facilities in many fields, especially in high-tech industries and quality inspection departments. The following is a detailed summary of the advantages of constant temperature and humidity clean rooms: 1. Provide stable environmental conditions Constant temperature: The constant temperature and humidity clean room