Quality Management System

Enterprise quality management.
Without the enterprise price.

You need AS9100 and ISO 9001 compliance. You need document control, audit management, CAPA tracking, and training records. What you don't need is a $75,000 QMS implementation that takes six months and requires a dedicated admin. IVIS QMS was built for organizations that need powerful quality tools at a price point that won't require a board approval.

AS9100
ISO 9001
EB 2678Q
IVIS QMS — Quality Dashboard
342
Controlled Docs
7
Open CAPAs
96%
Training Current
UPCOMING AUDITS
AS9100 Surveillance AuditMAR 15
Internal Quality Audit — MachiningAPR 02
ISO 9001 RecertificationJUN 20
Document Control

Every document. Every version. Every approval. Tracked automatically.

If your quality documentation lives in shared drives, email attachments, or worse — printed binders — you're running a quality system you can't trust. IVIS QMS gives you real document control: version management, approval workflows, automatic distribution, and a complete audit trail showing who changed what and when. Your auditor will see a system that's current, organized, and accountable.

Centralized document repository with version control
Approval workflows with electronic sign-off
Automatic distribution and read-receipt tracking
Full audit trail — every change logged with user, date, and reason
Document Control
📄QP-001 Quality Manual
v4.2 · Approved: Jan 15 · Owner: Quality Mgr
CURRENT
📄WI-042 Welding Procedure
v2.1 · Pending approval · Owner: Eng Lead
IN REVIEW
📄SOP-015 Receiving Inspection
v3.0 · Review due: Feb 28 · Owner: QA Lead
DUE SOON
Audit Management & CAPAs

When the auditor arrives, don't scramble. Pull up the dashboard.

IVIS QMS tracks internal and external audits, findings, corrective actions, and preventive actions in one place. Schedule audits, assign auditors, record findings, create CAPAs, and track them to closure — all with the evidence trail your AS9100 or ISO 9001 registrar expects to see. No more chasing down audit evidence the week before a surveillance visit.

Audit scheduling, planning, and findings management
CAPA tracking from identification through root cause to closure
Nonconformance reporting and disposition workflow
Training records tied to competency requirements and job roles
CAPA Tracker
CAPA-2025-003: Dimensional nonconformance on Part #4417
Root cause: Tool wear not detected · Due: Feb 28 · Status: Investigation
CAPA-2025-002: Supplier certificate missing for lot #882
Root cause: Receiving SOP gap · Due: Feb 15 · Status: Action Pending
CAPA-2025-001: Calibration schedule missed on CMM
Root cause: Manual tracking · Closed: Jan 30 · Status: Verified Effective
Why Switch

What QMS looks like when it actually works.

Most small manufacturers know their quality system has gaps. Here's what closing them looks like.

Without IVIS QMS

Quality docs in shared drives with no version control
CAPAs tracked in spreadsheets or not tracked at all
Audit prep takes weeks of scrambling for evidence
Training records maintained on paper or in HR's filing cabinet
Enterprise QMS tools cost $50K–$100K+ to implement

With IVIS QMS

Centralized docs with version control and approval workflows
CAPAs tracked from finding through root cause to verified closure
Audit evidence linked and ready — pull it up in seconds
Training records tied to roles, competencies, and due dates
Priced for the 100-person shop, not the 10,000-person enterprise
Get Started

Quality management that works for your size.
Not against your budget.

See how IVIS QMS gives you the structure, accountability, and audit readiness your registrar expects — without the implementation project from hell.

Also from IVIS

Quality + Compliance + Capacity. One platform.