Maintain equipment reliability while ensuring compliance with ISO, FDA, and GxP requirements. Automate quality workflows, reduce equipment-related risks, and drive operational excellence with a digital QMS designed for equipment management.
Maintain equipment reliability while ensuring compliance with ISO, FDA, and GxP requirements. Automate quality workflows, reduce equipment-related risks, and drive operational excellence with a digital QMS designed for the highest equipment quality.
In equipment manufacturing for highly regulated industries, quality management is critical. From component sourcing to final assembly and installation, each phase must meet rigorous design, safety, and documentation requirements.
Quality Forward’s eQMS enables complete lifecycle oversight of manufacturing operations, ensuring that equipment meets both performance and regulatory standards. Track quality events, enforce structured workflows, and maintain audit-ready records, all in one compliant platform.
Manage deviations, CAPAs, and supplier quality in a single unified system.
Ensure full traceability for components, calibrations, and validations.
Maintain compliance with FDA, ISO 9001/13485, GxP, EU MDR and more.
Track materials, components, and processes through the entire build cycle - from design to delivery, with complete visibility.
Manage engineering changes, supplier modifications, and manufacturing updates with built-in risk assessments and approval workflows.
Centralize audit trails and documentation for ISO, FDA, and customer inspections. Maintain validation records and proof of compliance.
Digitize SOPs, technical files, validation protocols, and installation records with version control and 21 CFR Part 11–compliant eSignatures.
Capture equipment deviations early and initiate structured investigations. Link directly to CAPAs for root cause resolution and prevention.
Gain real-time visibility into recurring issues, audit findings, and equipment trends. Leverage analytics to improve quality and reduce rework.
Purpose-built to support complex manufacturing cycles and field performance tracking.
Support fast-growing teams and global operations without adding complexity and cost.
Built for manufacturing environments and highly regulated industries.
Identify gaps, overdue training, and risky patterns before they become issues
Enterprise-grade infrastructure for speed, security, and stability
Meet FDA 21 CFR Part 11, ISO 9001/13485, EU MDR, and global GxP requirements out-of-the-box.
Capture deviations, nonconformances, or service issues from the field, floor, or lab in real time.
Use built-in tools to perform root cause analysis and risk evaluations tied to affected components or procedures.
Automatically trigger corrective actions or initiate change controls with full traceability and regulatory alignment.
Link controlled documents and updated SOPs directly to training assignments and equipment records.
Visualize recurring issues, overdue actions, and supplier-related equipment problems with live dashboards.
