2025-08-21
When planning a cleanroom, determining its classification is one of the most important steps. Cleanroom classification sets limits for airborne particles and ensures compliance with ISO 14644-1 and GMP standards.
Cleanroom classification defines the maximum number of particles per cubic meter at defined particle sizes. Different industries, including pharmaceuticals, biotechnology, electronics, and food, require different levels of cleanliness.
ISO Class | ≥0.1 µm particles/m³ | ≥0.5 µm particles/m³ | ≥5 µm particles/m³ | Typical Applications |
ISO 1 | 10 | — | — | Nanotechnology, semiconductor |
ISO 2 | 100 | 10 | — | Microelectronics |
ISO 3 | 1,000 | 35 | — | Optics, high-precision labs |
ISO 4 | 10,000 | 352 | — | Pharmaceutical filling support |
ISO 5 | 100,000 | 3,520 | 20 | Aseptic processing, operating rooms |
ISO 6 | 1,000,000 | 35,200 | 293 | Medical device assembly |
ISO 7 | — | 352,000 | 2,930 | General pharmaceutical production |
ISO 8 | — | 3,520,000 | 29,300 | Packaging, non-sterile manufacturing |
ISO 9 | — | 35,200,000 | 293,000 | Controlled environments |
GMP Grade | Area | Usage |
Grade A | Laminar flow workstation | Critical aseptic operations |
Grade B | Background for Grade A | Preparation for aseptic processing |
Grade C | Cleanroom | Less critical processing steps |
Grade D | Controlled area | Non-sterile processes |
Different industries have different requirements, for example pharmaceuticals must follow GMP and ISO 14644-1.
Processes involving sterile products need higher classification (ISO 5 / GMP Grade A).
FDA, EU GMP, and WHO guidelines dictate classification levels for specific industries.
Higher cleanroom classes are more expensive to build and maintain, so balance quality and budget.
We provide turnkey solutions for cleanroom planning, design, construction, and validation.
Pharmaceuticals, biotechnology, electronics, laboratories, food processing.
Contact GCC Cleanroom to discuss your project and receive a tailored classification plan.