2025-08-07
Clean room panels are fundamental building components that create controlled environments for drug production. These specialized wall, ceiling, and floor systems maintain sterility by preventing contamination from particles, microbes, and chemical vapors – directly impacting product quality and regulatory compliance.
Meet ISO 14644-1 cleanliness standards
Support HVAC and filtration system integration
Withstand frequent disinfectant exposure
| Panel Type | Core Material | Best For |
|---|---|---|
| Sandwich Panels | Aluminum/PU foam core | Walls & ceilings (ISO 5-8 areas) |
| FRP Panels | Fiberglass-reinforced plastic | Wet processes (antibiotic production) |
| Stainless Steel | 304/316L grade | Sterile fill lines (Grade A/B zones) |
| Anti-static Panels | Conductive coatings | API handling (OEB4+ compounds) |
Rapid installation/relocation for facility upgrades
Interlocking mechanisms ensure airtight seals
Pre-installed ports for:
Withstand:
GMP Requirements:
Validation Needs:
| Factor | Traditional Walls | Clean Room Panels |
|---|---|---|
| Installation Time | 8-12 weeks | 3-5 weeks |
| Lifecycle Cost | High maintenance | 10-15 year service life |
| Change Flexibility | Fixed structure | Reconfigurable modules |
Clean room panels are the unseen guardians of pharmaceutical quality. By selecting the right materials and designs, manufacturers achieve: