Pharmintech offer a range of Calibrations and Validations service for Equipments and Cleanroom facility based on the thorough understanding of cGMP standards.
We have wide range of services to concern for clean room validation by our panels of specialist with us.
We perform validations as per ISO 14644, EU cGMP, US Federal Standard 209E, USFDA, guidelines for all room classifications.
All testing, reports and certification is regulated by our operating process which constitute part of our Quality Manual.
Any parameter outside the allowable range will be reported immediately and strategies and measures will be put in position to correct abnormal activity.
Our Validation Services include
