Cleanroom Validation

Autocal provides an all-inclusive service in the qualification of clean rooms at your facility. We offer reassurance that the controlled environment is monitored to your specific requirements and applicable standards.


The quality of products manufactured not only depends on manufacturing techniques but also on the quality of environmental conditions. In conjunction with qualification of the clean rooms the associated ventilation systems must also be qualified. Qualification entails checking clean room facilities for compliance with relevant regulatory guidelines along with evaluation in terms of measurement and monitoring techniques.


Autocal offers qualification in the areas of:


Test conducted

Confirmation with Guide lines

  • Filter Air Velocity Test & ACPH Calculations
  • Filter Integrity Test (Using PAO/DOP)
  • Particle Count Test
  • Recovery Test
  • Air Flow Pattern Test
  • Air Pressure Balancing
  • Temperature & RH Measurement
  • Light Intensity Measurement
  • Sound Level Measurement
  • User Required Specifications
  • Functional Design Specification
  • ISO 14644
  • FS 209 E
  • BS 5295
  • EU GMP/ EC GMP
  • SCHEDULE M
  • WHO 2002
  • USFDA
  • As Specified by  User