QT9 QMS

QT9 QMS is a quality management system covering document control, CAPA, audits, deviations, risk analysis, complaint tracking, inspections, training and electronic batch records and device history records. The vendor's site describes modules for centralizing documents, approving CAPAs, scheduling audits, monitoring deviations, assigning risk scores, tracking complaints, capturing inspection data, managing training, and automating batch and device history records.

The product is positioned for regulated manufacturers, with the site listing medical devices, pharmaceuticals, aerospace, automotive, cannabis, chemicals, cosmetics, electronics, food and beverage, general manufacturing, metals and mining, and plastics as target industries. It can be deployed in the cloud or on-premise, and the site states it is pre-validated, including execution of Installation, Operational and Performance Qualification protocols, and lists support for standards such as ISO 13485, ISO 9001, AS9100, and FDA 21 CFR Part 11.

Pricing is not published. The pricing page states that QT9 QMS uses custom, quote-based pricing scaled by number of concurrent users, deployment choice (cloud or on-premise), implementation requirements and number of facilities, with a quote requested through the vendor. The site does not state specific integrations with named third-party systems for QMS beyond the related QT9 ERP product, nor does it give a concrete implementation timeline or numeric price. Deployment is described as either cloud or on-premise, so a single deployment model cannot be assumed without specifying which option a buyer selects.