BRIO digitizes audits, non-conformities, CAPAs, inspections, and competencies within an integrated industrial quality management system, designed to support ISO 9001 compliance and beyond.
The Quality module enables process standardization, non-conformance detection, corrective action execution, and regulatory compliance — without relying on paper.
Everything is fully traceable, accessible, and audit-ready.
Conduct standardized audits (GMP, HACCP, ISO, local regulations).
Use custom checklists by plant, production line, or process.
Record deviations with photos or videos.
Assign corrective and preventive actions (CAPA) with clear ownership and due dates.
A single repository for manuals, procedures, records, and SOPs.
Built-in version control and digital signatures.
Capture inspections from mobile devices (online and offline).
Manage sampling plans and laboratory results.*
Ensure personnel hold active certifications for critical tasks.
Receive alerts for expirations or missing requirements.
Link quality events with production, safety, or maintenance.
End-to-end traceability from supplier to final customer.*
Dashboards with KPIs: audits, CAPA closure rates, and deviations by plant.
Exportable reports for internal and external audits.
*Features under development or available to beta customers.
From deviation reporting to CAPA closure, BRIO supports the entire quality lifecycle.
Integrated with other areas, it enables fact-based decision-making and consistent standards across multiple plants.
Fill in your details and we’ll show you how BRIO can adapt to your operation.
