 |
|---|
 |
 |
 |
 |
 |
 |
Intech perform on-site HEPA & ULPA DOP Filter Integrity Testing (in accordance with British Standard BS EN 14644 Part 3) Calibration and Validation of Cleanrooms and associated equipment. Our engineers cover the whole of the UK and frequently travel to Europe.
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 customers.
The DOP filter testing and validation services we provide 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 • Airflow/Room Balancing • Smoke visualisation and video analysis tests |
 |
We also carry out tests on Room Air Change Rates and Differential Pressures, in accordance with the Orange Guide* and the NHS Health Technical Memorandum HTM 03-01. In the event of contamination it is important for customers to know that the air will be changed re-circulated at the appropriate rate, in accordance with site and regulatory requirements. Differential pressures between rooms must also be maintained and validated to prevent unwanted contamination entering or leaving a particular area.
Our engineers survey various hospitals, drafting detailed reports to confirm that the requirements of HTM 03-01Specialised Requirements For Healthcare Premises are being met. Where issues are identified and improvements can be made, our clearly presented reports make the implementing change a much easier task.
Energy conservation audits are performed to assess the efficiency of clean air systems and look for improvements in the operation of AHU units and Building Management Systems (BMS).
We offer Maintenance Contracts for AHU systems. A good preventative maintenance program is vital in providing maximum reliability with the minimum of downtime. Equipment testing frequencies must be set and adhered to as required by regulatory authorities and to help provide maximum equipment life.
All of our engineers are fully trained in cleanroom and GMP/cGxP practices for both Hospital and Pharmaceutical research and production facilities. Although we focus on the Pharmaceutical and Healthcare industries we are by no means limited to it. Current customers include the following industries: Healthcare, Pharmaceutical, Nuclear, Space, Electronic and the Semiconductor industry.Our team provide an SOP development service for the creation and amendment of SOP's and test procedures for your facility. Existing procedures can be re-written as the demands of your facility change.
*Orange Guide (MHRA Rules and Guidance for Pharmaceutical Manufacturers and Distributors 2007).
