Formalise, integrated approach to your management systems

When certifying to multiple ISO Standards management systems and complying to global regulations, you probably won’t need to start from scratch.

Our software makes it much easier to successfully achieve new ISO Standards as it brings all your management system documentation, risks, suppliers, internal reviews, training records, and more into a single system.

Associate each Standard and Regulation with business processes, policies and procedures, so it’s easy to manage any changes. Evidencing compliance is a natural part of daily business as all the controls, audit trails, and ownership responsibilities are embedded.

Furthermore, during our best practice implementation process, an expert member of our team will work with you to configure the solution. We’ll help you to understand what already works well and optimise the processes that could work better.

Browse ISO Standards and Regulations

Integrated software to make managing your regulatory and quality requirements natural and easy

Our software is used in 120+ countries to help achieve standards and meet regulatory requirements.
Annex SL
The ultimate prize for your business when implementing multiple management system standards is a truly integrated system. Our software makes it easy for you to implement Annex SL by enabling you to associate documents, horizontally manage processes and only update information once.
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ISO 9001:2015
Many tenders require ISO 9001:2015 to demonstrate a business has a formal and documented approach. Certification provides confidence that your business consistently delivers products and services that are fit for purpose. Use Qualsys's software to plan, document, report and continually improve your ...
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ISO 14001:2015
Achieving the prestigious ISO 14001 standard demonstrates to your customers you have responsible, robust environmental management processes. Our software and services provides you with a best practice framework to plan and manage all the requirements for ISO 14001.
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ISO 45001
Your customers want to deal with a safe, healthy business. Certification to ISO 45001 demonstrates to your customers you have a robust health and safety management system. Our software provides you with everything you need to properly plan, document and report on your health and safety management sy...
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ISO 13485
With increasing regulatory pressure to implement robust design controls, supplier accountability and risk-based thinking, many companies in the medical device industry opt to follow ISO 13485:2016 for a best practice framework. The Standard harmonises global medical device regulations, helping compa...
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ISO 14971
ISO 14971 defines international requirements for risk management systems for medical devices. Our software helps you to implement best practices throughout the entire lifecycle of your medical device.
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ISO 19011
The ISO 19011 standard provides guidance on auditing management systems. It applies to all businesses who need to conduct internal or external management system (MS) audits, or manage audit programmes. Our software provides a best practice framework for managing your audits.
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ISO 22301
Disaster can strike at any time, whether it's due to extreme weather, faults with technology, human error or deliberate wrongdoing. Being able to respond quickly and effectively to this kind of disruption is crucial if your business is to survive.
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ISO 27001
You're not only contending with the effects of digitisation, big data and the 'Internet of Things', but the growing demands of globalisation, regulation and protection against cyber threats. ISO 27001 gives you a framework. We provide the tools to help you apply it.
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BRC
BRC 7 promotes best practice and helps you ensure your business is working to strong, consistent standards. By gaining BRC certification, you assure your customers that you're monitoring and improving the quality and safety of your product. Our software helps you manage all your processes, policies ...
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AS 9100
With the AS 9100 Rev D transition deadline creeping ever closer, it is important to get your policies, processes and systems in order. Qualsys works with a series of aerospace manufacturers, including HybridAir Vehicles, Tritech and GET Ltd. Learn more about how our solutions aid compliance to AS 91...
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IATF 16949
Design and development defects. Production waste. Product variation. All bring increased costs, delays and compliance issues for automotive manufacturers. Let us help.
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General Data Protection Regulation (GDPR)
With potential fines of €20 million or 4% of annual turnover for failure to comply with the new General Data Protection Regulation, implementing an integrated information and data compliance management system is no longer a choice. Our software provides you with a cost-effective, essential busines...
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ISO 22000
ISO 22000 provides a framework for your food safety management system. Our software and services help you plan and manage a system that truly reflects best practice.
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FDA
Use Qualsys's software to get control, visibility and confidence that your business complies with the FDA (Food and Drug Administration).
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MHRA software
Our software helps you to manage compliance to the MHRA. Plan, manage, record and optimise your performance using our software.
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GMP software
Use our software to get traceability and accountability, ensure GMP, and keep your people safe.
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GxP software
Qualsys's software provides a framework for a risk-based approach to change management of your GxP management system.
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Design Control software
Design controls is a formal methodology required for medical device development. Here's how Qualsys's quality management software helps manage design controls to meet FDA, ISO 13485 and MHRA requirements.
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