PRODUCTS
QMS
Manage quality records, actions and approvals in a traceable workflow.
Controlled quality workflows
CPI QMS manages nonconformities, CAPA, change control, audits and related quality processes with configurable states, responsibilities and approvals.
Process coverage
Configure the modules around your procedures.
Corrective and preventive actions
Root-cause analysis and action tracking
Change control
Internal and external audits
Training and competency relations
Electronic approval and revision history
Traceability by design
Every decision, assignment, approval and revision remains connected to the underlying quality record.
Control and traceability
Make the lifecycle of a quality record transparent.
Role- and state-based task routing
Due date, delay and escalation tracking
Required field and evidence controls
Change history across user, time and revision
HOW IT WORKS01 02 03 04
From quality event to closure
A quality event is not only recorded; it is managed with ownership, evidence, approval and change history.
Record
A deviation, nonconformance or change starts through a controlled record.
Assessment
Risk, root cause and required actions are evaluated by authorised roles.
Action
CAPA tasks, due dates and owners are tracked through workflow.
Closure
The process cannot close until required evidence, approvals and history are complete.
FAQ
Frequently asked questions
Does QMS impose a fixed procedure?
No. Forms, states, approval chains and responsibilities are configured around the organisation’s procedures.
Is change history auditable?
Subject to configuration, the system can retain who changed what and when as part of the controlled record.
Can QMS integrate with other systems?
ERP, document, training or laboratory integrations are designed around ownership of data and process boundaries.
Digitize your quality processes
Model your procedures, responsibilities and approval chains with our team.