CALIBRATION MANAGEMENT
Now Part of Blue Mountain
Paperless calibration planning, execution, and certification for manufacturers who answer to auditors.
Since 1990, CompuCal has helped regulated manufacturers replace paper calibration records with controlled digital workflows. As part of Blue Mountain, that calibration depth now sits alongside 35+ years of GMP asset management experience.
In life sciences and other regulated environments, calibration is not a task you close and forget. It is evidence. Every interval, every as-found reading, and every out-of-tolerance investigation becomes part of the record an auditor will ask to see. CompuCal replaces manual, paper-based calibration with controlled digital workflows for planning, execution, certificate generation, and traceability.
Plan and schedule calibration work by interval, usage, or asset criticality
Execute calibrations against controlled procedures with defined tolerances
Generate certificates and reports without manual transcription
Retrieve complete calibration history when an auditor asks for it
CompuCal covers the calibration lifecycle in one system, from the schedule that triggers the work to the certificate that closes it.
Schedule calibration tasks by time interval, usage, or asset criticality, so due dates surface before they go overdue.
Keep a secure, traceable log of calibration activity, with user history and electronic sign-off on every record.
Link calibration tasks to specific instruments, equipment, and locations for clear ownership and control.
Match your existing calibration procedures with configurable steps, tolerances, and approval stages.
Send reminders for upcoming, overdue, and failed calibrations by email or in-app.
Track schedules and certification status for reference equipment, and flag standards that are expired or non-conforming before a technician uses one.
Produce traceable, statistically valid uncertainty evaluations with the built-in uncertainty budget module.
Capture, complete, and sign off calibration work in the field with CompuCal GO, online or offline.
21 CFR Part 11 sets the requirements for electronic records and electronic signatures in FDA-regulated environments. Compliance is a property of your validated system and your procedures, not of software on its own. CompuCal supplies the technical controls that make that validated state achievable, and the documentation that helps you demonstrate it.
Capture signatures with user authentication, and record who signed, what they signed, and when (21 CFR 11.50).
Maintain secure, computer-generated, time-stamped audit trails of user actions, changes, and approvals (21 CFR 11.10(e)).
Enforce role-based permissions and authentication so only authorized users reach regulated records (21 CFR 11.10(d)).
Store records so they stay accurate, attributable, and readily retrievable across the full retention period (21 CFR 11.10(c)).
Run in a validated environment, with documentation that supports your installation, operational, and performance qualification work (21 CFR 11.10(a)).
CompuCal GO puts assigned calibration work in the technician’s hand. Pull up procedures, tolerances, and required tools on a phone or tablet, record as-found and as-left values as you work, and sign off without walking back to a desk.
Reporting
Each calibration completed in CompuCal creates a record of the triggering interval, procedure, readings, and final sign-off. Reporting draws directly from that record.
You’re not rebuilding evidence after the fact. Reports use the same data captured during execution, so reviewers see the work as technicians recorded it.
Generate certificates and reports directly from values captured during calibration execution, without manual transcription.
Purpose-built for metrology since 1990
35+ years serving life sciences
Validated records, complete traceability
Connects to SAP and other enterprise systems
