Nonconformance Management (NCM) Software

Modernize Nonconformance Management with Trackmedium eQMS

Trackmedium's Nonconformance Management (NCM) module streamlines how you capture and resolve nonconforming events across the organization. Whether issues are found during inspections, reported by customers, or triggered through audits, the system helps teams investigate root causes, apply corrective actions, and close the loop in a structured and audit-ready way.

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Standardized Nonconformance Workflow

Guide each nonconformance through structured steps from detection to closure with clearly defined roles, statuses, and routing.

Root Cause and Containment Tracking

Capture immediate containment actions and identify root causes using structured fields and investigation tools.

Disposition Management

Select appropriate resolutions such as rework, scrap, return, or use-as-is, with optional deviation tracking when exceptions apply.

Linked CAPA and SCAR Creation

Trigger corrective or supplier action requests directly from nonconformance records and track their resolution within connected workflows.

Follow-up Action Tracking

Assign tasks with due dates, monitor progress, and escalate overdue actions to ensure accountability and timely closure.

Centralized and Configurable Platform

Securely store all records, manage access, and tailor workflows, forms, and notifications with full support for mobile and tablet access.

Nonconformance Lifecycle at a Glance

Trackmedium supports a complete nonconformance workflow from initial detection through closure.

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Connected Platform

Trackmedium NCM works seamlessly across the eQMS platform to ensure traceability and alignment.

CAPA

Launch and link CAPAs or Supplier Corrective Action Requests (SCARs) from any nonconformance. Both are managed in the CAPA module for streamlined follow-up and resolution.

Audit Management

Convert audit findings into NCMRs with one click and ensure all issues are documented and tracked.

Temporary Deviation Management

Automatically trigger deviation workflows when "use-as-is" dispositions are selected, ensuring full traceability and formal approval for exceptions.

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Why Trackmedium eQMS?

Trackmedium helps quality teams close the loop on issues quickly, maintain compliance, and drive continuous improvement

Maximize Efficiency

Automated workflows reduce manual work, shorten resolution times, and ensure nothing falls through the cracks.

Ensure Compliance and Traceability

Capture every step with a full audit trail to meet regulatory and internal quality requirements.

Connect the Dots Across Quality

Link NCMRs to CAPAs, audits, deviations, and related processes for complete oversight and accountability.

What Our Customers Are Saying

Trackmedium eQMS is proud to provide simple, globally accessible quality management solutions across all industries.

"Trackmedium eQMS has all the modules our organization requires to ensure systems are functional, and remain in compliance, while providing visibility and communication to our company. [It] ensured our users were completely trained and the system was operational in a remarkably short amount of time."

Larry Tyler
Quality Systems Manager

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"The system is purchased with access to all available applications making it flexible to your needs. It is also customisable meaning that where an application doesn't quite fit your needs you can work with the Trackmedium team to easily customise to your requirements. This has made it a valuable and flexible tool in our company."

Catherine Bennett
Head of Quality and ESG

*Source: ^footnote1

"Finally I have found a system that is both highly functional, fully linked between modules and flexible. I have tried many systems over very many years, but never found one that actually meets all my requirements - until Trackmedium. I thoroughly enjoy using this system."

Jane Wymer
QHSE Coordinator

*Source: ^footnote1

Frequently Asked Questions

What types of nonconformances can we manage?

Track product, process, supplier, customer, and internal deviations.

Can I launch CAPAs or SCARs from the NCM record?

Yes. You can initiate and monitor them directly from within any NCMR. Both are managed within the CAPA module.

Is the system mobile-friendly?

Yes. The platform works seamlessly on tablets and smartphones.

Can I configure the workflow and forms?

Yes. You can customize fields, steps, user roles, and alerts to fit your process.

Can we track costs?

Yes. You can record cost impact fields and include them in reports or dashboards.

Does the system support escalations?

Yes. Due dates and reminders can be configured to send alerts and escalate overdue actions.

Can users attach documents or evidence to an NCMR?

Yes. Attach images, files, related documents, or links to any record.

Is Trackmedium NCM compliant with ISO and FDA standards?

Yes. The module is designed to support ISO 9001, ISO 13485, ISO 14001, IATF 16949, and FDA 21 CFR Part 820.

Can I manage NCMRs across multiple sites or departments?

Yes. The system allows location-based filtering, access control, and reporting.

Can we restrict access to sensitive nonconformance records?

Yes. You can control who can view, edit, or approve records based on roles, departments, or locations.

Is there reporting or dashboard functionality?

Yes. You can generate real-time reports and dashboards by product line, cause, location, or custom fields to identify recurring trends.

Does the system support electronic signatures?

Yes. Trackmedium supports secure electronic signatures to meet compliance requirements like FDA 21 CFR Part 11.

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Take Control of Nonconformances
Resolve quality issues at the source with a connected, compliant, and fully configurable platform.

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