Cleanroom Validation & Testing Service
Validation is the core link to confirm whether your cleanroom meets international regulatory standards and passes official inspection. We provide full-cycle one-stop cleanroom validation testing service, matching the whole EPC project process, covering pre-construction risk assessment, installation qualification (IQ), operation qualification (OQ), performance qualification (PQ) full set of validation content.
Our professional testing laboratory team is equipped with imported professional testing instruments, and can complete all standard testing items required by ISO 14644, GMP and FDA certification: airborne particle concentration detection, viable microorganism monitoring, airflow pattern visualization test, indoor positive/negative pressure difference detection, temperature and humidity uniformity test, filter integrity PAO leak test, lighting & noise detection, recovery rate test of sterilization equipment, cleanroom self-cleaning cycle verification.
We will sort out complete standardized validation documents according to the industry you belong to, including test raw data records, instrument calibration certificates, test trend analysis reports, deviation handling records, compliance summary files, which can be directly used for official audit, factory inspection and certification application.
For pharmaceutical factories, medical device workshops and biosafety laboratories that need to pass national and international regulatory inspections, our validation service can effectively avoid non-compliant test data and document defects, shorten the certification cycle of your workshop, and help your production line quickly obtain legal production qualification after delivery. We support regular periodic re-testing and annual validation maintenance services to keep your cleanroom always in a certified compliant state during long-term operation.
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