Qualityze

Incoming, in-process, final and supplier inspections with AQL or LTPD sampling, then accept, reject, hold or conditional release, and an NCR or reinspection.

Risk-based prioritisation, 5 Whys, Fishbone and 5W-5H root-cause tools, and an effectiveness check before approval and closure.

Standard templates, reviewer due dates, reminders, version-to-version comparison with comments, e-signatures and release control.

Assignments by role, location or SOP update, assessments of understanding, and certification sign-off with completion certificates.

The audit page describes planning and executing audits online and offline; device support and sync rules need a demonstration.

The QMS agent recommends next actions from historical nonconformance records and answers natural-language questions; each other suite has its own agent.

SSO, MFA, role-based access, a full audit trail, e-signatures and an API-first design are listed as built-in platform capabilities.

Capture a nonconformance with product, process, site, supplier, batch or lot context; assess risk, contain affected material, choose repair, scrap, return, concession or rework, and escalate higher-risk or systemic events to CAPA. Confirm the Nonconformance and CAPA module entitlements and disposition authorities.

Maintain supplier records and time-sensitive documents, qualify suppliers with questionnaires, manage SCAR collaboration, and track performance with configurable scorecards across approval, remediation and requalification. Confirm supplier-portal and audit entitlements in the quote.

Plan recurring internal, external, supplier, customer, safety, regulatory and compliance audits; define scope and criteria, assign findings, escalate to CAPA, verify action effectiveness, and retain closure reporting and audit history. Offline execution is documented for audits only and requires a device-specific demonstration.