Around the globe, organizations, and laboratories that perform testing, calibration and/or sampling activities deal with the ever-increasing challenge of being able to demonstrate confidence in their operations, prove they operate in a competent and impartial way, and are able to provide valid results.
ISO/IEC 17025 allows organizations and laboratories to show that they operate competently and can generate valid results, therefore promoting confidence in their work both nationally and internationally. Furthermore, the regulation helps ease collaboration between laboratories and other bodies by creating wider acceptance of results between countries. This means that certificates and test reports can be accepted amongst various countries without having the need for further testing, reducing bureaucracy, saving time and reducing costs.
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Calibration record
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Calibration event
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Calibration execution
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Resource control
Main Benefits
Automate scheduling of calibrations, maintenance and repairs.
Support automatic and real-time data acquisition through serial ports, eliminating manual data entry.
Support Type A and Type B measurement uncertainties.
Recall management controls with fixed time intervals, real-time usage, maintenance, and repair.
Choose calibration/maintenance based on frequency or usage.
Automate calibration procedures.
Maintain and retrieve master equipment, calibration history and measurement data records.
Store all calibration information safely and efficiently.
Traceability to in-house equipment calibration and Reference (or National) Standards.
Secure access control for individual users with password protection.
Automatically flag equipment found to be out of calibration, in use, or out for maintenance or repair.
Maintain a secure audit trail and standards traceability.
Conduct independent equipment R&R studies.
Know some success stories
Featured Resources
Ebook
13 Processes Every Enterprise Quality Management Software (EQMS) Should Automate
This eBook will show how to get the true value that an EQMS promises by automating 13 quality processes.
White Paper
How will ISO 13485:2016 impact your relationship with suppliers?
The importance of the "risk based approach" for the correct performance and adequate safety of medical devices.