Clean Room Validation By Cadillac Engineering Works

CleanRoom Validation/ HVAC Validation We provide and extensive range of services pertaining to clean room validation by our panel of expert professionals. Applications Pharmaceutical Sectors Hospital Sectors Scientific Research & Development sectors Diagnostic & Pathology Lab Food & Beverages Sectors FMCG Sectors   Objects Pharmaceutical Processing Zones Operation Theatres (OT) Critical Care Units (CCU) Microbiology/QC Laboratories Laminar Air Flow Benches (LAF) Bio-safety Cabinets Sampling Booths Dispensing Booths Fume Hood etc.   Standards /Guidelines we follow   ISO 14644 US FEDERAL 209E GMP SCHEDULE M NABH CDC ISO 8995 ISO 3741 ISO 10816   CADILLAC carries out following tests to validate clean rooms/clean zones.   *Particle Count Test *DOP Test/PAO Test/HEPA Filter Integrity Test *Air Velocity Test/ ACPH measurement *Airflow Visualization Test *Temperature and Humidity Test *Room Pressurization Test *Recovery Test *Light Intensity Test *Noise Level Test *Vibration Level Test *DQ/IQ/PQ/OQ Documentation   Equipment List for Clean Room Validation Sl. No. Testing Parameter Equipment Used 1 DOP/PAO HEPA Filter Integrity Test }  DOP Generator }  DOP Photometer   2 Particle Count Test }  Laser Particle Counter   3 Room Pressurization Test }  Differential Pressure Gauge   4 Airflow Visualization Test }  DI Water Fogger }  Digital Camera   5 Recovery Test }  DOP Generator }  Laser Particle Counter   6 Temperature and Humidity Test }  Digital IR Thermometer }  Digital Thermo-Hygrometer   7 Air VelocityTest/Air Change per Hour Calculation(ACPH) }  Digital Vane Type Anemometer }  Digital Hot Wire Anemometer   8 Noise Level Test }  Noise Meter   9 Light Intensity Test }  LUX Meter   10 Vibration Level Test }  Digital Vibration Meter