Instrument/Equipment Validation
This equipment validation service is specifically for compliance with the Food & Drug Administration Standards (FDA), and the Medicines & Healthcare products Regulatory Agency (MHRA).
Having precise instruments or equipment in a lab environment is of the utmost importance, because even the slightest inaccuracies can lead to false results, Our equipment validation will thus make sure that your data is as accurate as possible.
Our services cover a range of different aspects of validation. We can test the electrical connections, utility supply, and safety compliance, as well as the critical calibration of your devices. These are just a few of the tests that we must take in order to validate your instruments.
Aughton technicians follow a strict validation process. Such a process can be separated into five distinct categories:
- Design Qualification (DQ) – This step assesses whether or not the initial design could meet the practical needs of the customer.
- Installation Qualification (IQ) – We properly install the equipment, then test for performance.
- Operational Qualification (OQ) – We will then test the equipment for functionality across the whole system.
- Performance Qualification (PQ) – We monitor the equipment for some time to ensure that it displays the correct measurements.
- Component Qualification (CQ) – We will also check other components and parts periodically, and subject them to random quality tests.
Contact Us
If you have any questions about our equipment validation services, or would like to book an appointment, then please contact us here.