Enterprise Solutions

Quality Management (QMS)

Compliance-ready quality, connected to your ERP

Overview

Document control, CAPA, audits, training, and supplier quality in a validated system built for regulated industries.

For regulated manufacturers, quality can't live in binders and shared drives. Our QMS solutions digitize document control, change management, CAPA, nonconformance, complaints, audits, and training — with the electronic signatures and audit trails that FDA 21 CFR Part 11, ISO 13485, and ISO 9001 demand. We integrate quality events directly with ERP transactions so quality and operations finally share one record.

Why teams choose it

  • Pass audits with confidence — everything is traceable
  • Cut CAPA cycle times dramatically
  • One quality record across quality and operations
  • Part 11-compliant signatures and audit trails
Capabilities

What Quality Management (QMS) covers

Configured to your processes — not the other way around.

Document Control

Versioned, routed, and approved documents with controlled distribution.

CAPA & Nonconformance

Structured investigation, root cause, and effectiveness verification workflows.

Audit Management

Internal, supplier, and regulatory audit planning, execution, and findings.

Training Management

Role-based training matrices with automatic assignment on document change.

Supplier Quality

Approved supplier lists, SCARs, and incoming inspection integration.

Validation Support

IQ/OQ/PQ protocols and documentation for regulated deployments.

Ready to see Quality Management (QMS) in action?

Tell us where you are and where you're headed. We'll give you a straight answer on scope, timeline, and cost.