Data-driven management reviews. Zero manual reporting.
Pull live data from audits, CAPAs, incidents, training, and risks into structured management review meetings. Automated agendas, action tracking, and trend analysis replace spreadsheets and slide decks.
No credit card required · No long-term contract · UK-based support · Live in 4 weeks
Trusted by quality teams at 500+ organisations
Everything You Need for ISO 9001 Quality Management
Click any capability to explore how it works.
Document Control
Version-controlled documents with approval workflows, controlled distribution, and automatic revision tracking. Never lose a document again.
Explore →CAPA Management
End-to-end corrective and preventive action workflows with root cause analysis tools including 8D, 5-Why, and Ishikawa diagrams.
Explore →Nonconformance Tracking
Log, categorise, and trend nonconformances. Automatic escalation rules ensure nothing slips through the cracks.
Explore →Audit Management
Schedule internal and external audits, assign auditors, build checklists against ISO 9001 clauses, and track findings to closure.
Explore →Management Review
Auto-generated management review packs with quality KPIs, audit summaries, CAPA status, and customer satisfaction data.
Explore →Supplier Quality
Supplier scorecards, qualification tracking, incoming inspection records, and automated alerts when quality thresholds are breached.
Explore →See Your Quality System Before You Sign Up
Explore the five key areas of Q-Hub QMS. Click a tab or let it auto-advance.
Your Quality Command Centre
See every quality KPI in a single view: open NCRs, CAPA completion rates, audit scores, supplier performance, and document compliance. Real-time data means you always know where you stand before an auditor walks in.
Every Document, Controlled and Current
Full version history, multi-step approval workflows, and controlled distribution ensure your team always works from the latest approved revision. Superseded documents are automatically archived with complete traceability.
From Problem to Prevention
Every CAPA follows a structured workflow: identify, contain, analyse root cause, implement corrective action, and verify effectiveness. Built-in 8D, 5-Why, and Ishikawa tools ensure your team addresses the real problem, not just the symptom.
Audit Programme That Runs Itself
Plan your annual internal audit schedule mapped to ISO 9001 clauses. Assign auditors, track completion, and automatically link findings to CAPAs. Always know your audit status at a glance.
Management Reviews in Minutes, Not Weeks
Auto-generated review packs with all the inputs required by ISO 9001 clause 9.3: audit results, customer feedback, NCR trends, CAPA status, supplier performance, and quality objective progress. Present to leadership with confidence.
The Quality Management Lifecycle
Plan, Do, Check, Act — click each stage to learn more.
Plan Your Quality Management System
Define your quality policy, objectives, and measurable targets. Identify context of the organisation, interested parties, and risks and opportunities per ISO 9001 clause 4-6. Q-Hub provides templates and frameworks to structure your planning and ensure nothing is missed.
Document & Control
Create and approve your quality manual, procedures, work instructions, and forms. Every document goes through a configurable approval workflow, is assigned a revision number, and is automatically distributed to the right people. Superseded versions are archived with full traceability.
Execute & Monitor
Track nonconformances, manage CAPAs, monitor supplier quality, and measure process performance against your quality objectives. Real-time dashboards give you visibility into every aspect of your quality system without waiting for month-end reports.
Audit & Assess
Execute your internal audit programme with ISO 9001 clause-based checklists. Record findings, raise CAPAs, and track corrective actions to closure. Generate audit reports that demonstrate conformity to your certification body and build confidence in your quality system.
Review & Improve
Feed audit findings, NCR trends, CAPA data, customer feedback, and supplier performance into your management review. Identify improvement opportunities, set new targets, and drive continual improvement. The PDCA cycle starts again, each time raising the bar.
Stop Emailing Documents. Start Controlling Them.
Paper-based quality systems and shared drives fail audits. Q-Hub gives you electronic document control with version history, multi-step approval workflows, controlled distribution, and automatic archiving of superseded revisions. Your certification body will see a document register that is always current, always traceable.
- Full version history with side-by-side comparison
- Configurable approval workflows with e-signatures
- Automatic read receipts and overdue notifications
Close CAPAs 70% Faster
Spreadsheet-based CAPA processes lose visibility, miss deadlines, and fail audits. Q-Hub automates the entire workflow: from nonconformance identification through root cause analysis, corrective action, effectiveness verification, and closure. Overdue CAPAs trigger automatic escalation to keep your quality system on track.
- Built-in 8D, 5-Why, and Ishikawa tools
- Automatic escalation on overdue actions
- Effectiveness verification with scheduled follow-ups
Connects With Your Existing Tools
Q-Hub fits into your tech stack. Connect in one click with single sign-on, data sync, and automated workflows.
Calculate Your Quality Cost Savings
Enter your current quality workload to see how much Q-Hub could save your team.
Your Current Workflow
Your ROI Results
Your Quality Data Is Safe With Us
Hover to learn about each certification and commitment.
Stop Managing Quality in Spreadsheets
Go Live in 2-4 Weeks
A structured rollout with dedicated support at every stage. Click each milestone to see what happens.
Setup & Configuration
- Dedicated quality implementation manager assigned to your account
- Organisation structure, departments, and user roles configured
- ISO 9001 clause framework and document hierarchy established
- SSO, branding, and integration connections set up
Document Migration
- Quality manual, procedures, and work instructions imported with version history
- Historical NCR, CAPA, and audit records migrated
- Supplier quality data and approved supplier lists transferred
- Data validation and integrity checks completed
Training & Enablement
- Quality manager admin training: system configuration, workflows, and reporting
- Quality engineer training: NCR logging, CAPA management, and root cause tools
- Auditor training: audit scheduling, checklist execution, and finding management
- End-user training: document access, read receipts, and action completion
Go Live & Ongoing Support
- Supervised first internal audit with your implementation manager
- 30-day hypercare period with priority support
- Quarterly business reviews to optimise your QMS configuration
- Ongoing UK-based support via chat, email, and phone
What Our Quality Teams Achieved
Watch the 3-Minute QMS Demo
See how Q-Hub transforms document control, CAPA management, and audit scheduling into one seamless quality platform.
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QMS Software Questions
Yes. Q-Hub maps directly to ISO 9001:2015 clause requirements. Document control, CAPA management, internal audits, management reviews, and nonconformance tracking are all structured around the standard's requirements, giving you audit-ready evidence at all times.
Every document has full version history, approval workflows, and controlled distribution. Authors draft, reviewers approve, and the system automatically notifies affected users of new revisions while archiving superseded versions. Read receipts confirm that employees have acknowledged new documents.
Yes. From nonconformance identification through root cause analysis (8D, 5-Why, Ishikawa), corrective action assignment, effectiveness verification, and closure. Every step is time-stamped and auditable. Overdue actions automatically escalate to keep your quality system on track.
Manufacturing, aerospace, automotive, medical devices, food manufacturing, pharmaceuticals, and any organisation pursuing or maintaining ISO 9001 certification. Our customers range from 20 to 10,000+ employees across single and multi-site operations.
Most QMS implementations go live within 2-4 weeks. A dedicated implementation manager guides you through setup, document migration, user training, and go-live. Complex multi-site deployments may take 4-6 weeks depending on data volume.
Yes. Supplier scorecards track delivery performance, quality metrics, audit results, and nonconformances. Set qualification criteria and receive alerts when suppliers fall below thresholds. Manage your approved supplier list with periodic re-qualification workflows.
Plans start from £99/month for quality management. All plans include a 14-day free trial with full access. See pricing →
Deepen Your Quality Knowledge
Free guides, templates, and webinars to help you build a world-class quality management system.
The Complete Guide to ISO 9001 Implementation
Step-by-step implementation guide covering every clause of ISO 9001:2015 with practical tips for first-time certification.
Read the guide Template · FreeCAPA & Root Cause Analysis Template
A ready-to-use template covering 8D methodology, 5-Why analysis, and Ishikawa diagrams for effective corrective actions.
Download template Webinar · 40 minFrom Paper to Digital: The QMS Transition Playbook
Watch our recorded webinar on digitising your paper-based quality system without disrupting operations.
Watch webinarWorks Seamlessly With
See Q-Hub QMS in Action
Replace spreadsheets and paper with a purpose-built quality management system. Book a personalised demo today.