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Maintaining a contamination-free environment is critical in pharmaceutical manufacturing. Cleanroom classification systems help define the necessary air cleanliness levels in different zones to ensure drug safety and regulatory compliance. This guide breaks down four key frameworks you should know: US FED STD 209E, ISO 14644-1, cleanroom design requirements, and EU GMP Annex 1. 1. US

Modular cleanrooms are prefabricated cleanroom systems designed for quick assembly, cost efficiency, and flexible adaptation. They use standardized components to meet various cleanliness levels (ISO 1–9), serving industries like semiconductors, biopharma, and laboratories. 1. Advanced Air Filtration & Airflow Control Modular cleanrooms maintain air purity using HEPA/ULPA filters and fan filter units (FFUs) integrated into

Many people wonder: “My clean room is already built, but the cleanliness level is not sufficient. Can I upgrade it?”The answer is: Absolutely yes. Whether you’re working with a modular clean room or an engineering-based clean room, upgrades are possible—though the process, complexity, and cost can vary significantly. Here’s how to systematically upgrade your clean

Optimized Blog Content: What Are the Real Requirements for a 100,000-Class Cleanroom? Many assume that building a 100,000-class (ISO 8) cleanroom is simply about meeting a cleanliness rating. In reality, several other crucial conditions must be met to maintain this classification and ensure stable, high-quality production. Let’s explore the key requirements. 1. Cleanliness Level A

Before deciding to build a dust-free workshop, scientific research laboratories need to comprehensively consider many factors to ensure that the special needs of scientific research are met. Because the dust-free workshop is a key environment for scientific research experiments to ensure the accuracy of experiments and the reliability of results. First of all, we need