Corrective Maintenance
Root cause, corrective action and verification on every repair.
Corrective Maintenance formalises the repair process beyond the breakdown clock — capturing the diagnosed cause, the corrective action taken, parts consumed and a verification step before the asset returns to GxP use.
What Corrective Maintenance delivers
A controlled path from start to closure
- 1Diagnose
- 2Plan Repair
- 3Execute
- 4Verify
- 5Sign Off
- 6Close
Why teams move to Corrective Maintenance
Document every repair to a defensible, signed standard
Feed accurate cause data into reliability analysis
Escalate recurring failures into CAPA automatically
Control repair cost with visible labour and parts data
Give QA confidence in return-to-service decisions
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.