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Audit Management
Optimize Quality, Ensure Compliance with Seamless Audit Management
Whether you're managing internal audits, supplier audits, or regulatory compliance reviews, Trackmedium's eQMS Audit Management module ensures end-to-end visibility and control across the audit lifecycle. From planning and checklist execution to audit findings, Corrective Action initiation, and final report distribution, all activities are centralized, automated, and fully traceable.
Standardized Audit Templates
Create reusable audit types and checklist templates that can be tailored for different audit categories.
Audit Planning & Scheduling
Easily schedule recurring or ad-hoc audits with automated reminders and team assignments.
Checklist-Based Auditing
Assign checklists to individual auditors. Include required questions, scoring logic, and document links.
Integrated Corrective Actions and Nonconformances
Create and track corrective actions or nonconformance records directly from audit findings.
Customizable Report Generation and Distribution
Generate audit reports using your own branded template. Export to Excel or PDF and distribute to stakeholders with one click.
Role-Based Access Control
Control who can view, create, or manage audits by role, location, or department.
Connected Platform
Trackmedium's eQMS Audit module integrates seamlessly with other Trackmedium QMS modules:
End-to-End Audit Lifecycle
Trackmedium's eQMS Audit Management module supports the complete lifecycle:
Create, Define audit type, scope, purpose, location, participants, and required checklists.
Schedule, Plan recurring or one-time audits with date-based triggers and assignment logic.
Conduct, Perform audits on tablet or desktop, complete checklists, and assign findings.
Capture, Log nonconformances, recommendations, and initiate CAPAs directly from checklists.
Report, Generate full audit reports, export results, and track distribution.
Close, Complete audit workflows, verify CAPAs, and retain all history for future reference.
Built for Compliance, Ready for Any Industry
Trackmedium eQMS Audit Management helps you exceed audit expectations and stay compliant across industries:
Regulated Industries
Ideal for organizations that must comply with global regulations and standards such as ISO, FDA, and 21 CFR Part 11.
Non-Regulated & Growth-Focused Sectors
Perfect for companies seeking to strengthen quality culture, reduce operational risk, and improve efficiency - even without formal compliance mandates.
Why Trackmedium eQMS?
Trackmedium eQMS helps quality teams close the loop on issues quickly, maintain compliance, and drive continuous improvement.
Complete Lifecycle Coverage
Manage everything from audit creation to final report and Corrective Action follow-up in one unified system.
Gain Real-Time Insights
Monitor audit progress with dashboards, track checklist completion, and generate audit-ready reports to identify trends and risks early.
Secure and Scalable Cloud Platform
Trackmedium eQMS runs on a secure, scalable, and compliance-ready cloud infrastructure with full audit trails, role-based access, and e-signature support.
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
Quality Systems Manager
*Source: footnote 1
"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
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
Can we track findings and launch Corrective Actions directly from audits?
Yes. You can initiate Corrective Actions directly from audit findings or checklist responses. These are automatically linked for full traceability.
Can we create nonconformance records during the audit?
Yes. Nonconformances (NCMRs) can be created from checklist questions or audit observations and optionally escalated to Corrective Actions.
Can audits be performed from a tablet or mobile device?
Absolutely. Trackmedium is fully responsive and allows auditing on desktop, tablet, or mobile devices.
Can we set up recurring audits automatically?
Yes. Through the Audit Plan feature, you can schedule recurring audits with predefined checklists and teams.
Can we create different checklists for different audit types?
Yes. Each audit type can be associated with one or more checklist templates. These checklists can include scoring logic and required questions.
Does the system support external audits or supplier audits?
Yes. You can initiate internal, external, or supplier audits and define participants, including external users, if needed.
How are audit reports generated and distributed?
Audit reports are generated with a single click and can include findings, Corrective Actions, NCMRs, participants, and checklist results. You can export to PDF or Excel and email reports to internal or external contacts.
Can we control who sees or edits audit data?
Yes. Role-based access controls allow you to define permissions by role, location, or department to ensure secure and segmented access.
Is there version control for audit templates or checklists?
Yes. Audit Types and Checklists are version-controlled to ensure auditors always use the latest approved templates.
Can we attach SOPs or documents to audits?
Yes. You can link documents from the Document Control module to audit records, checklists, or specific questions.
How does the system ensure auditor qualification?
You can integrate with the Training module to track auditor training status and restrict audit assignments to qualified users.
Is Trackmedium compliant with ISO and FDA regulations?
Yes. Trackmedium supports ISO 9001, ISO 13485, AS9100, and FDA 21 CFR Part 11 requirements, including audit trails, e-signatures, and full traceability.
See more questions
Ready to Take Control of Audits?
Close the loop on quality faster, reduce risk, and gain total oversight.
Close the loop on quality faster, reduce risk, and gain total oversight.
