Intech Process Solutions

UKAS Calibration Services and Cleanroom Validation
Intech specialises in providing Calibration Services and Cleanroom testing and validation services to a range of industries from pharmaceuticals, process, electronics and measurement to museums and medical
We also offer a wide range of laboratory and on-site traceable (non-accredited) calibration services. The on-site calibration services we offer range from a single days work through to annual contracts with engineers permanently located on a customer's site.
Our engineers use a variety of state of the art test equipment that is routinely calibrated and maintained to ensure regulatory compliance. We can calibrate a vast range of instrumentation including temperature, humidity, pressure, differential pressure, pH, conductivity, weights & scales, flow etc.
We supply individuals and teams consisting of Calibration Technicians, Reliability Engineers and Process Engineers and can also offer Commissioning/Decommissioning services to numerous areas of industry.
Intech personnel are well qualified and well motivated individuals who ensure constant and consistent delivery of our high standards. Training is at the forefront of staff progression and you can be assured that highly competent quality engineers are looking after your requirements.
No matter how large or small Intech will provide the solution to your needs.
Intech carries out on-site HEPA Filter Testing in accordance with British Standard BS EN 14644
Part 3.
We offer extremely competitive rates and can work out of hours, at weekends and during shut down periods so as to provide a minimal disturbance service to the customer.
The services we offer include the following:
HEPA Filter testing on Air Handling Units (AHU's)
HEPA Filter Testing in changing rooms
HEPA Filter Testing in cleanrooms
HEPA Filter Testing of safety cabinets
HEPA Filter Testing of fume cupboards
HEPA Filter Testing of laminar flow cupboards
Cleanroom Particle count testing
We also carry out tests on Room Air Change Rates, in accordance with the Orange Guide*. In the event of contamination it is important for customers to know that the air will be re-circlulated at the appropriate rate, in accordance with site and regulatory requirements.
Energy conservation audits can be performed to assess the efficiency of clean air systems and look for improvements in the operation of (for example) AHU units.
All of our engineers are fully trained in cleanroom and GMP practices for both Hospital and Pharmaceutical research and production facilities. Although we focus on the Pharmaceutical industry we are by no means limited to it. Current customers range from Healthcare/Pharmaceutical to wafer diffusion production facilities in the semiconductor industry.