QMS
Quality management software for ISO 9001 and related management system standards. The quality department’s entire workload — from documents to nonconformities, from internal audits to management review — in one place; the system exists to answer “where is the evidence?” during an audit.
- Who it is for
- Quality managers and process owners; organisations within certification scope
- Size
- 179 data tables
122 screens - Last change
- 21 Sep 2026
258 commits
qms · Prisma schema · model count · measured 13 Oct 2026
What QMS solves
Brings documents, nonconformities, audits, risk and management review into one system and produces the evidence at audit time.
Document and record control
Document management, distribution and controlled-copy tracking, e-signatures and retention and disposal periods in one place. Which version is held by whom is read from the system.
From nonconformity to a lasting fix
Nonconformity and nonconforming-output records, corrective and preventive action (CAPA), 8D problem solving and a shared action pool run linked together.
Audits and certification
Internal audits, external audits and certification tracking; the evidence needed going into an audit is prepared from the system as an audit evidence pack.
Risk and prevention
Risk and opportunity assessment, FMEA (failure mode and effects analysis), control plans and measurement system analysis (MSA) in the same system.
Resources, competence and suppliers
Training and competence, equipment and calibration, supplier management, organisation and authority definitions — the resources the quality system relies on, on record.
Management and performance
Management review, objective and indicator tracking, cost of quality, customer complaints and satisfaction; results are followed on dashboards.
Interface layout
The drawing below shows the product’s screen layout. The interface is in Turkish and the rows are examples; we walk through the real screens in the demo.
Interface drawingShows the product’s layout; the interface is in Turkish and the rows are examples.
Highlights
- Documents, controlled copies and e-signature
- Nonconformity · CAPA · 8D
- Internal audit and audit evidence pack
- Risk · FMEA · control plan
Maturity
Product address: qms.cscodebilisim.com
The same discipline, continued
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Every laboratory process, from sample receipt to accredited report, on one platform.
ISO/IEC 17025ITSM
Answers “What is IT doing, how long does it take, what do we have?” with evidence.
ITIL 4 · ISO/IEC 20000-1Contractor Management Portal
Collects the documents of contractors coming on site in one flow; once every department involved has approved, the company and its staff are cleared for the site.
OHS Law No. 6331Request a QMS demo
Instead of a ready-made demo script, we show the product with an example from your own everyday work; what fits and what doesn’t becomes clear faster in the first meeting.
We reply the same day.