Services / Calibration
We calibrate and manage the critical instrumentation of your plants in regulated environments, ensuring traceability, data integrity compliance and operational continuity.
We don't manage calibration on Excel sheets: we use Dimacs, our proprietary platform that keeps over 11,000 instruments under control. Add to that a presence in regulated sites that dates back to 1990.
Frequently asked questions
What metrology, maintenance and Quality Assurance managers ask before entrusting the calibration of a pharmaceutical site's instruments.
A GMP provider does more than calibrate: it manages schedules, certificates, traceability and Out of Tolerance events with an audit trail. Eurosystem manages the metrology of more than 11,000 instruments in pharmaceutical sites with its proprietary Dimacs platform, calibrates on site and in the lab, and guarantees traceability with standards calibrated at ACCREDIA-accredited laboratories.
By comparison with a traceable reference probe in a thermostatic bath or dry-block, at points covering the real operating range (for example 2-8 °C for cold rooms, 121 °C for autoclaves). The result, with declared uncertainty and acceptance criterion, feeds the certificate and the schedule; an out-of-tolerance result triggers the batch impact assessment.
You need ACCREDIA traceability of the reference standards, not an accredited certificate for every field instrument. Reference standards are calibrated at LAT centres; plant instruments are calibrated by comparison with those standards, keeping the chain documented. Eurosystem is not a LAT centre: it is the partner managing the whole metrology system and guaranteeing its traceability.
The interval is defined per instrument based on criticality, historical stability and manufacturer recommendations, and justified in writing. Typical intervals range from 6 to 12 months for critical instruments; reviewing historical data allows them to be extended or shortened with evidence.
It is calibration performed in the plant with traceable portable standards. It pays off when removing the instrument means downtime or damage risk, and when it must be calibrated under real operating conditions. The result goes straight into the schedule and audit trail.
In Dimacs every certificate is linked to the instrument, the standard used and the intervention, with electronic signature and an Annex 11 compliant audit trail. During an inspection the certificate of any instrument is available in seconds, together with its history.
Learn more
GMP calibration
Images of activities and instrumentation related to metrology management: the value of calibration lies in care for method, traceability and documentation.
Request a site visit or a quote: we respond with a concrete proposal.
