Calibration Management
Instrument calibration schedules, due alerts and tolerance results.
Calibration Management schedules, executes and evidences instrument calibration against traceable standards, locking out non-compliant instruments and keeping every result audit-ready.
What Calibration Management delivers
A controlled path from start to closure
- 1Schedule
- 2Notify
- 3Calibrate
- 4Record Results
- 5Approve
- 6Release for Use
Why teams move to Calibration Management
Prevent use of instruments outside calibration due date
Evidence calibration compliance without a scramble before audits
Link out-of-tolerance findings directly into deviation handling
Keep calibration history attached to results it produced
Reduce the administrative load of managing paper calibration logs
Built for regulated operations
21 CFR Part 11
Electronic records and electronic signature controls — unique user identity, secure e-signatures and computer-generated audit trails on every record.
EU GMP Annex 11
Computerised system controls including access management, change control, data integrity and periodic review of the system.
GAMP 5
Risk-based validation approach, with pre-executed IQ/OQ documentation supplied with every release.
ALCOA++
Records that are attributable, legible, contemporaneous, original and accurate — enforced at record level.
OPS IQ is designed to support these regulatory expectations. Compliance is achieved together with your own validated implementation, procedures and controls.
Connected to your enterprise systems
ERP / SAP
Master data, materials and batch context exchanged over open REST and event APIs.
MES
Shopfloor execution events and equipment context linked to quality records.
LIMS
Laboratory results and specification data connected to quality decisions.
Identity Providers
Enterprise SSO and role-based access through your existing identity provider.
Enterprise APIs
Open REST and event APIs for custom and legacy systems.