CLEANROOM
VALIDATION
Tecomak can provide a comprehensive test and maintenance solution
for virtually any clean air device or cleanroom facility. We
are committed to our clients' needs and aim to be the preferred
choice for cleanroom validation.
 Why
is the Tecomak validation service better?
- High calibre, professionally qualified site engineers
- Continual investment in staff training
- Concise, customised, professional test reports
- Latest test equipment
- Full engineering support service
We can validate to all international standards including ISO
14644: 1999, EEC GMP: 2002, Fed Std 209E: 1992, BS 5295: 1989
and IES-RP-CC006.2.
 What
test procedures are offered?
- Air velocity and volumetric flow rate measurement
- Room differential pressure testing
- Filter integrity leak testing (DOP method)
- Airborne particle counting
- Airflow visualisation and digital video analysis
- Construction joint integrity testing
- Recovery performance testing
- Airflow balancing
- Temperature monitoring
- Lighting levels checks
- Noise level checks
- Pressure and flow gauge calibration
For details on clean air cabinet servicing please click
here.
We invest in the latest test equipment to ensure that test
data is accurate and reliable.
Advancing Our Standard of Service
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The pharmaceutical industry has been concerned for some
time about the need for formal qualification of test engineers.
To address this important issue, all Tecomak Validation
Engineers are professionally qualified, having obtained
the CTCB qualification for Cleanroom Testing in association
with Glasgow University.
The quality of reports supporting cleanroom validation
is paramount. We take pride in the presentation and quality
of all our documentation and maintain a quality system
accredited to ISO 9001: 2000.
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