Quality and Compliance go hand in hand. For manufacturing businesses, they are critical components for the safety, quality and profitability of products made, while guaranteeing that all legal regulations are followed.
For manufacturers, maintaining strong quality and compliance standards is critical not just for product integrity, but for operational efficiency, profitability, and legal assurance. Failing to meet these standards can lead to production delays, customer dissatisfaction, reputational damage, regulatory penalties, or even costly product recalls.
Quality and Compliance must be demonstrated and many systems/ software are used to do this such as spreadsheets, Forms and Quality Management systems (QMS). Let's explore how a Quality & compliance focused document management system could enhance your processes further.
Quality reflects how well a product, service, or process meets defined requirements or customer expectations. It’s often linked to reliability, performance, and consistency.
Compliance involves meeting the legal, regulatory, and ethical standards relevant to your industry or jurisdiction. This includes:
Government regulations (e.g., GDPR, HIPAA, SOX)
Industry standards (e.g., ISO, PCI-DSS, AS/NZS)
Internal policies and codes of conduct
Contractual obligations or client requirements
A document management system allows business to demonstrate their compliance credentials. When used in Quality based processes, often alongside a Quality Management System, (QMS), document management software helps to gain process transparency, increasing efficiency and minimising risk.
Operations stay within legal boundaries, and the organisation remains audit-ready at all times. It also enhances transparency and accountability, which are increasingly important in today’s business environment.
Managing documents properly with uniform Quality and Compliance processes helps safeguard valuable employee and customer data. Integrated Digital Forms are used to great effect with our Quality Focused clients for all types of policies and forms like Accident Forms, Repair Requests, and policies such as SOPs.
With the implementation of a dedicated document management system, by centralising and securing documentation, businesses can streamline processes, strengthen data protection, and ensure regulatory readiness across departments.
For all documents stored to DocuWare, document control is enforced and ensures that only authorised individuals have access to sensitive information and a process is followed using workflows where required.
The differing levels of access that organisations require, such as strict editing rules for policies and manuals, or read only rights for Standard Operating Procedures and instructions can be achieved with a document management system.
Document control software provides certainty that the most up-to-date information is readily accessible, and that previous versions are only visible to users with certain permissions.
It is essential to have an audit trail of document revisions which demonstrates the effectiveness of any quality system in place. However, this should not come at the cost of killing efficiency within the business.
Most modern quality departments have a quality management system (QMS) in place that may come with a small level of document control within it. But more often than not, it makes sense to have a separate, integrated document management system (DMS) to allow none QMS users to get involved in the quality processes.
Dedicated document management software can often be more cost effective, especially where it can also be used for other processes such as accounts payable approvals.
Organisations today face growing pressure to manage increasing volumes of data, meet strict regulatory requirements, and uphold quality standards all while maintaining operational efficiency. This blog might help you to consider if now is the right time for your organisation to start a document management software implementation.
A Document Management System (DMS) is a powerful tool that helps streamline Quality based processes, reduces risk, and improves visibility across the organisation. Here are the main areas where a DMS makes a measurable impact for Quality and Compliance:
Paper-based storage is costly, inefficient, and vulnerable to physical risks such as fire, theft, or misplacement. Certain records like policies, accident forms, none conformances, contracts, and other documents must also be retained for specific legal periods.
A DMS allows organisations to digitise and securely store documents in the cloud, drastically reducing physical storage needs and costs. Automated notifications and access controls further ensure sensitive files are only visible to authorised users and can be deleted when no longer needed.
For Quality departments, maintaining control over policies, procedures, manuals, and incident reports is vital — but managing these processes manually often leads to inconsistencies, delays, and version control issues. DocuWare Forms simplifies this by digitising how information is captured and stored. Instead of relying on paper forms or static PDFs, staff can complete structured electronic forms that automatically route to the right people for review or approval. This ensures every submission is captured accurately, time-stamped, and linked directly to related documents such as procedures or training records, creating a fully traceable audit trail.
When it comes to incident or non-conformance reporting, DocuWare Forms really shines. Employees can submit incident details from any device, attach supporting evidence, and trigger automated workflows for investigation or corrective action. Managers are instantly notified, response times improve, and all actions are securely recorded for compliance and ISO audits. By integrating with your existing quality management system, DocuWare provides a single, secure repository for all quality-related documents — reducing admin time, supporting continuous improvement, and strengthening your overall compliance posture.
Manual document retention practices (e.g. spreadsheets or email reminders) are prone to error and can put your business at risk of non-compliance.
With DocuWare, automated retention policies can be applied based on document type, status, or creation date. For example, financial records can be set to auto-delete after six years ensuring compliance with statutory requirements while avoiding unnecessary data hoarding.
As hybrid and remote work becomes the norm, effective version control is more important than ever. With teams accessing and editing documents from multiple platforms like SharePoint, Dropbox, or shared drives there’s a growing risk of conflicting versions or lost updates.
A DMS provides seamless version control by ensuring users can only access the most current document. During edits, the document is locked and read-only for others, preventing overlap or confusion. Once saved, it receives a new version number, and a full audit trail is maintained for traceability and compliance.
This is especially valuable for documents such as policies, procedures, and global standards where consistency and accuracy are essential.
Whether you're preparing for an ISO 9001 audit or conducting internal quality reviews, having the right documentation readily available is critical.
A DMS supports a smoother audit process by providing:
Instant access & history of required documents
Search filters by category, supplier, document type, or department
Logs showing who accessed or edited a document and when
This level of transparency strengthens your organisation's ability to demonstrate compliance, accountability, and process improvement while reducing the time and stress typically associated with audits.
Discover how The Woodland Trust uses a DMS to manage Gift Aid documentation and streamline audit preparation.
Our extensive range of products can help your business on its digital journey. Suitable for organisations of any size, and as simple or as complex as you need them to be.
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