Manufacturing
Connect procedures, production issues, supplier controls, equipment, and corrective work.
The connected quality platform
Quality, without
Quality, without
the complexity.
One practical eQMS for documents, training, quality events, corrective actions, audits, and more. Bring the work together and see what needs attention.
Connected workflows. Clear ownership. Traceable quality records.
CONNECTED BY DESIGN9 CORE MODULESCONFIGURABLE WORKFLOWSTRACEABLE RECORDS
One system for the work that matters
Every quality process
has a place here.
Replace scattered files, spreadsheets, and follow-up emails with a clear workspace for managing quality work from start to finish.
01
Document Control
Author, revise, route, and maintain controlled documents with history and approvals.
Explore module → 02Training Management
Connect role-based requirements, assignments, completion, and training visibility.
Explore module → 03Quality Events
Record and work through nonconformances, deviations, complaints, and investigations.
Explore module → 04Corrective Actions
Investigate causes, assign actions, review effectiveness, and close the loop.
Explore module → 05Change Control
Evaluate impact and risk, route decisions, and track implementation through closure.
Explore module → 06Risk Management
Assess risk, document controls, and review residual risk as actions progress.
Explore module → 07Audit Management
Plan audits, capture findings, assign follow-up, and track closure.
Explore module → 08Supplier Management
Maintain supplier qualification, assessments, performance, and quality history.
Explore module → 09Asset Management
Keep equipment records, maintenance, calibration, and validation status visible.
Explore module →Connected by design
Follow quality work across the system.
A quality event can prompt a risk review. A corrective action can lead to a change. A changed procedure can call for updated training. METIS keeps these steps in view so teams can follow the work and its records.
Illustrative workflow. Linkage and routing depend on how your METIS QMS workspace is configured.
Explore the platform- 01Quality eventCapture the issue and its context
- 02Risk reviewAssess impact and possible controls
- 03Corrective actionInvestigate, assign, and verify
- 04Change controlEvaluate and implement a change
- 05Documents & trainingUpdate procedures and learning
Built for quality-intensive work
Quality structure that
fits your operation.
Use a connected system to support your own quality processes and the standards or customer requirements that apply to your organization.
Aerospace
Organize quality records, risk reviews, audits, and process change in one workspace.
Testing laboratories
Keep technical records, equipment status, training, and improvement activities visible.
Growing quality teams
Build consistent processes as teams move beyond shared drives and manual trackers.
Designed around the workflow
Bring the details and decisions into view.
Configure quality event steps, assess risk, and review the records that connect the work.
QMS consulting services
Expertise to support the system.
Practical support for QMS development and improvement, internal audits, gap assessments, and clear next steps for your team.
Explore Consulting ServicesResources & insights
Practical guidance for better quality systems.
QMS & eQMS
“Use As-Is” Is a Disposition, Not a Shortcut
Make clear, documented decisions when a product or output does not meet requirements.
Read article → QMS & eQMSNot Every Change Needs Change Control
Learn when a formal impact review, approval, and implementation plan make sense.
Read article → QMS & AuditsIf Your Internal Audits Never Find Anything
Move beyond checklist auditing and follow how work moves across processes.
Read article →A clearer way to manage quality
Make the whole system easier to see.
See how METIS QMS can support the way your team works.
Book a Demo