Quality Management Software
Automate compliance instead of chasing it in spreadsheets.
Why teams choose 247 Labs
We have delivered compliance and quality management software for manufacturers for more than a decade.
Clients value systems that make ISO 9001 audits easier instead of harder.
Our team has shipped QMS platforms, integrations, and custom compliance tools for regulated manufacturers.
Challenge Map
Close the gaps that put your certifications at risk.
Quality management fails when non-conformances live in spreadsheets, CAPA follow-up falls through the cracks, or document control can't prove operators are using the latest approved procedures.
Non-conformances get logged in spreadsheets that nobody follows up on.
We engineer automated CAPA workflows that escalate, track, and resolve corrective actions instead of letting them stall in someone's inbox.
Common starting point for most QMS projects.Operators can't always tell if they're using the latest approved procedure.
We build secure, version-controlled document repositories so the shop floor always works from the current, approved standard operating procedure.
Useful for teams facing repeated audit findings.Quality data lives outside your MES and ERP, so holds don't stop production.
We connect your QMS to MES and ERP through secure APIs so quality holds automatically pause production when metrics fall out of tolerance.
Best for teams with disconnected quality systems.Services
QMS services for manufacturers protecting their certifications.
We scope QMS work around the compliance gap causing the most risk, whether that's CAPA tracking, document control, or system integration.
QMS readiness assessment
Review current quality processes, audit findings, and system gaps before scoping a build.
Custom QMS development
Build a quality management system tailored to your specific compliance and process needs.
CAPA workflow automation
Automate corrective and preventive action routing, escalation, and resolution tracking.
Document control systems
Build version-controlled repositories that keep operators on the latest approved procedures.
Supplier quality portals
Track supplier performance and issue digital corrective action requests through a secure portal.
MES and ERP integration
Connect QMS to production systems so quality holds trigger automatically when needed.
Case Studies
Manufacturing case studies with measurable outcomes.
Automating Sales and Order Management for Village Juicery's Growth
25% improvement in order processing
247Labs implemented an automated sales and order management platform that integrated seamlessly with Village Juicery's existing systems. The platform allowed for real-time order tracking, automated inventory management, and improved communication between staff and suppliers, ensuring a smooth workflow from order placement to delivery.
Read case study →
HUB International: streamlined project management for efficiency
Faster, more consistent project delivery
247 Labs rebuilt a fragmented project workflow into a structured system with clearer tracking and accountability, the same discipline CAPA and document control workflows need to hold up under audit.
Read case study →
World Vision: a data validation engine for large-scale accuracy
Improved data accuracy at scale
247 Labs built a data validation engine to catch errors across large, complex datasets, the same rigor QMS platforms need to keep non-conformance and audit records accurate.
Read case study →Capabilities
The workflow, document, and integration support needed to stay audit-ready.
We help teams automate CAPA, control documents, and connect quality data to production without adding manual work.
Map your compliance gaps
We review audit findings, CAPA backlogs, and document control gaps before building anything.
- Compliance gap analysis
- CAPA backlog review
- Build versus extend review
- Audit trail requirements
Build automated workflows
We create CAPA routing, document control, and inspection tools around your process.
- CAPA workflow automation
- Document control systems
- Supplier quality portals
- MES and ERP integration
Keep the floor compliant
We focus on operator-friendly inspection tools and fewer manual quality steps.
- Digital inspection forms
- Equipment data capture
- Exception handling flows
- Mobile quality checks
Stay audit-ready
We build immutable audit logs and access controls so records hold up under review.
- Immutable audit logging
- Role-based access controls
- Version-controlled documents
- ISO 9001 reporting support
Tech Stack
QMS should connect inspections, documents, and production into one record.
We build around the systems that make quality data trustworthy and audit-ready.
247 Labs delivered a web platform that not only looked exceptional but performed exactly the way our data models required. They took the time to understand the analytical demands behind the front end and built something that genuinely supports how we work. It was one of the smoothest development engagements I have been part of.
Malak Ahmad — Data Analyst, Deloitte
Business Benefits
Quality management should protect your certifications, not put them at risk.
The payoff comes from faster CAPA resolution and audit-ready records.
Fewer compliance surprises
Catch non-conformances early with automated CAPA routing instead of spreadsheet follow-up.
Audit-ready documentation
Keep version-controlled SOPs and immutable audit logs ready for external review at any time.
Faster CAPA resolution
Escalate and track corrective actions automatically so issues get resolved, not forgotten.
Stronger supplier accountability
Track supplier quality performance and issue corrective requests through a secure portal.
Connected production holds
Trigger automatic quality holds in MES and ERP when metrics fall out of tolerance.
Ready to automate compliance instead of chasing it in spreadsheets?
Talk with 247 Labs about your CAPA backlog, document control gaps, and the QMS build that fits your certification needs.
Start Your QMS ProjectFAQ
Common questions before a QMS project starts.
Custom QMS development means engineering a platform that automates and enforces your specific quality control processes, document management, and compliance workflows to meet strict regulatory standards.
Off-the-shelf QMS platforms are often rigid and force you to alter proven quality processes. Custom QMS matches your exact compliance needs and you own the system with no recurring licenses.
Yes. As an ISO 9001 certified company ourselves, we understand strict document control, CAPA management, and audit trail requirements, and we build QMS platforms specifically to maintain that compliance.
Yes. We build custom middleware to pull data directly from digital calipers, CMM machines, and other testing equipment into the QMS, eliminating manual data entry errors.
Let’s build something
great together.
We’re happy to answer any questions you may have and help you determine which of our services best fits your needs.
Call us at 1-877-247-7421 or email hello@247labs.com
Your Benefits:
- Client Oriented
- Independent
- Competent
- Result-driven
- Problem-solving
- Transparent
What happens next?​
1
We schedule a call at your convenience
2
We do a discovery and consulting meetingÂ
3
We prepare a proposalÂ
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