Clean Room Inspection

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• Clean room testing, validation & inspection services.
• Enhancing life by improving the quality of air.
• Good manufacturing Practices (GMP).

We at PioCal provide assistance to our clients to prepare the documentation required for equipment requalification in Pharmaceutical and food Industry. We ensure that your plant meets your business objectives while being fully compliant with the latest Good Manufacturing Practice regulations and standards.

Documentation preparation for:

• Qualification Protocols Writing and Execution
• Installation, Operational and Performance Qualification for Manufacture, processing related to various equipment and utility equipment
• Validation Master Plan
• Commissioning Plan
• Witnessing of Supplier Testing Activities
• Inventory of Process Equipment and Utilities
• User Requirement Specifications
• Clean Room Qualification
• Temperature Mapping Services

 The compression of ambient air leads to concentration of the contaminants which are present in the air and can also introduce other contaminants such as Oil vapor, Condensed water and Bacteria. We at PioCal can monitor the quality of compressed air against quality standards, give the accurate results and advice our customers about the various risk factors. Compressed Air validation is a critical component in the production of pharmaceutical industry and effects the quality of the end product. It is used in various operations in different industrial sectors including oil and gas, Pharmaceutical, Manufacturing, nuclear, diving and in medical applications. 

PioCal Services conduct Cleanroom Inspection includes the following:

• Air velocity and volumetric flow rate measurement
• Room differential pressure testing
• Filter integrity leak testing (DOP method)
• Airborne particle counting
• Airflow visualisation
• Airflow balancing
• Temperature monitoring
• Lighting and noise levels checks
• Pressure and flow gauge calibration
• UV level checking in laminar and pass boxes