Maintenance Plans:Our service team covers all statutory requirements to monitor the performance of all clean air devices as well as a wide range of environmentally controlled systems complete with a fully comprehensive repair service. Services also include Cleanroom validation, testing and controls calibration.
Once your facility is up and running we can provide all your after-care services for Cleanrooms, laboratories, aseptic suites, HVAC systems, air-conditioning systems, fume cupboards, water systems and many more. Our service department will also carry out any small works which may include any necessary modifications or upgrade requirements.
Costly downtime can be avoided by undertaking regular maintenance via our Planned Preventative Maintenance programmers which are site specific and detailed fully within our quotations. Our highly skilled service engineers are available on call at a moment's notice to respond to any unexpected occurrence or emergency which may occur.
We offer national coverage for call-outs, PPM Service & Maintenance and any other Cleanroom repairs. This is not limited to just Cleanroom & built facilities and systems, but those installed by others.
Cleanroom Area Validation:Cleanroom Validation Process:- Density and integrity test of the HEPA filters
- Classification (up to 0,1 µm)
- Recovery times
- Measurement and adjustment of the air velocity
- Microbiological tests (surface and air)
- Measurements of temperature, humidity
- Measurements of light intensity
- Visualisation of airflow patterns
- Tests on your networks of compressed air (particles, microbiological, dew points)
- Laminar flow, biosafety cabinet, fume hood, isolator
Projects governed by regulatory compliance promote a structured approach to delivery, running through the project from design inception to handover. This life cycle validation from URS, VMP, DQ, IQ and OQ require an understanding of more than just the mechanical parts and build components.
From high specification aseptic facilities, cleanrooms, specialist containment and other controlled facilities, we offer compliance to cGMP and cGLP standards to meet the stringent expectations of the associated regulatory bodies. With experience of delivering licensed facilities for the MHRA and FDA as well as other regulators including VMD and MDD, we offer a comprehensive service.
Preliminary compliance assessments are all carried out in-house through simple 'flow mapping' whilst early consultation with the specific regulator forms an integral part of our on-going design development. With independent third parties employed for all physical testing, you can be assured of robust checking procedures.
