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Modular Clean Room
Clean Room For Electronics
Cleanrooms are rated based on air purity, specifically the number of particles 0.5mm or larger per cubic foot, according to the U.S. Federal Standard 209E and internationally recognized ISO 14644 standards. These standards require detailed particle count measurements to determine cleanliness levels. In the UK, the classification has been under British Standard 5295, which is transitioning to BS EN ISO 14644
📌 Optimal Product Quality: Ensures minimal particulate presence for high-quality, defect-free electronic components.
📌 Enhanced Reliability: Protects sensitive electronics from particulate damage, boosting product longevity.
📌 Strict Contamination Control: Employs advanced HEPA or ULPA filters for continuous air purification.
📌 Standardized Cleanliness: Categorizes rooms by specific cleanliness levels for consistent control.
📌 Safety and Hygiene: Mandates specialized garments to reduce human-sourced contamination.
📌 Enhanced Drug Purity: Minimizes particulate contamination, ensuring high-quality pharmaceuticals with consistent effectiveness.
📌 Reduced Contamination Risk: Protects sensitive drugs from microbial and particulate contamination, increasing safety.
📌 Regulatory Compliance: Meets strict cleanliness standards required by health authorities for drug manufacturing.
📌 Product Integrity: Maintains consistent environmental conditions, preserving the stability and efficacy of medications.
📌 Worker Safety: Enforces protective attire to prevent human contamination and maintain a sterile environment.
Clean Room For Pharma
