ISO 9001 quality management software
QMOS links the daily records behind a quality management system. Follow an audit finding through corrective action, assigned work and an evidence-based effectiveness decision.
Control information and resources
Publish documents through review and approval and assign read tasks to affected staff. Keep training and competence records alongside equipment and calibration follow-up.
Turn findings into improvements
Containment, root cause, actions and effectiveness review are distinct stages in the corrective action workflow. Audit programmes, findings and management reviews provide inputs for the next improvement cycle.
- Actions with owners and due dates
- Risk and opportunity assessments
- Quality objectives and progress records
Evidence still needs judgement
Adapt starter templates to your actual processes. Completed fields alone do not demonstrate an effective system; your authorised team evaluates performance and decides what further action is needed.
QMOS supports records and workflows; it is neither an ISO certificate nor a certification guarantee. In-app approvals are not qualified electronic signatures. The ISO 13485 module is in pilot; authorised people remain responsible for regulatory, conformity and release decisions.
Frequently asked questions
Can we begin with document control?
You can plan a staged rollout. Agree the modules, roles and first processes during the demonstration and setup.
When should a corrective action close?
After the work is completed and an authorised person evaluates effectiveness against the recorded evidence. Completion alone is insufficient.