Cleanroom & Containment Validation

Premier LEV arranges cleanroom validation, microbiological environmental monitoring and biocontainment suite validation through specialist engineers. We help you define the testing programme, coordinate the site visit and obtain clear records for your quality team.

Request a cleanroom testing quote or call 0161 884 4200.

Cleanroom testing and classification

We arrange airborne particle counting for room classification, airflow volume and velocity measurements, pressure-difference checks, airflow visualisation, room recovery testing, and temperature and relative humidity measurements. Installed HEPA filter integrity testing can be included in the programme.

Share the required cleanliness classification, room layout and intended use. The specialist agrees the applicable methods, acceptance criteria, sampling locations and room state before testing. Where ISO 14644 classification or pharmaceutical requirements apply, these are defined in the project scope rather than assumed from the room name.

Microbiological environmental monitoring

Arrange active air sampling, settle plates and contact plates as part of an agreed monitoring programme. We confirm sampling locations, methods, handling and laboratory arrangements, reporting requirements and the site-specific interpretation criteria before the visit.

This service assesses environmental microbiological conditions within the agreed sampling scope. It is separate from microbiological safety cabinet performance testing.

Biocontainment suite validation

We coordinate a validation programme matched to the facility, containment requirements and proposed activities. Send the room specifications, containment level, previous reports and site protocols so that suitability and the exact testing scope can be confirmed. Access, decontamination, shutdown arrangements and any specialist restrictions are agreed before booking.

Installation and operational qualification: IQ/OQ

Our specialists can execute agreed installation qualification (IQ) and operational qualification (OQ) protocols. Supply your approved documents, equipment or room requirements and acceptance criteria. We agree responsibilities for recording results, reporting deviations and submitting completed records for your quality review.

Protocol execution and test results support your qualification process; final site or process approval remains subject to your own quality procedures.

Plan your visit and reporting

Send the site postcode, room list, drawings, previous reports, required tests and preferred dates. Premier LEV remains your point of contact, with specialist work delivered through specialist engineers. Your quotation identifies the tests and records included, with follow-up or remedial work agreed separately.

See HEPA filter testing and management and our laboratory and cabinet services, or send your cleanroom requirements.