— Focused on cleanroom compliance, we perform qualification to ensure facilities and equipment meet specs. Scope covers cleanroom performance (cleanliness class, temp/humidity, differential pressure, air change rate), equipment (air showers, disinfection units) and HVAC & automation systems. We issue full GMP-compliant protocols, records and reports. Our expert team pinpoints hidden risks with reliable data to help clients pass audits and maintain stable operation.
Three Core Supports
— Documentation System: Complete risk-based validation documents underpin the whole system.
— Professional Team: Dedicated validation crew arranges manpower, schedule and budget for pharmaceutical projects.
— Full Coverage: In line with GMP, we carry out required qualification to confirm effective control of all critical production factors.
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