Fitter, faster, healthier businesses

Getting products which are safe and fit for purpose to market requires a culture of quality.

To do this, you need systems which provide a best-practice framework for all your business processes.

Our software and best practice implementation and CSV services help you create a life science quality management system which will support you in planning, communicating, validating and optimising your processes.

 

Expert GAMP 5 computer system validation

Qualsys works in partnership with you from day one to ensure you have the appropriate documentation, records and considerations for your validation master plan and traceability matrix.

From validation test scripts to providing support during your audits, validation training to ongoing careful management of system upgrades, we ensure you are confident, prepared and more resilient to manage change.

Complex circle

Why life science businesses choose Qualsys

Instant reporting

Always have access to the cost of poor quality so you know what's working, what's not and a plan for improvement.

Protect your brand

With all this data and trend analysis at your fingertips, you'll be able to anticipate problems before they even occur.

Designed for busy leadership

The dashboard, to-do lists and notifications provides leadership with high-priority issues to address.

Avoid penalties and fines

Best practice audit trails and electronic signatures protect your business enables you to demonstrate business diligence, protecting you from fines and penalties.

Reinforce best practice

Through continuous review and improvement, your system provides a framework for good governance, risk and compliance.

A happier, healthier business

Give confidence to your auditors, employees and customers.

Integrated modules for life science quality and compliance management

What you can manage in EQMS by Qualsys
Audit management software
Audit management software
Too many businesses hope that when an external auditor is examining their business they don’t uncover any issues. But this approach causes stress, encourages a reactive culture and exposes the business to high levels of risk. A regular and thorough internal auditing programme helps you identify an...
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Document control software
Document control software
Modern technology means we are bombarded with information. The challenge is making sure the right information is viewed by the right person at the right time. Document Manager by Qualsys provides a comprehensive and powerful solution for the distribution and control of all types of crucial documenta...
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Equipment maintenance software
Equipment maintenance software
Over 70% of organisations have no formal method for managing how equipment is used, maintained and eventually replaced, or for ensuring there’s a qualified person on-site to operate that equipment. Managing business equipment correctly is crucial if your organisation is to compete in the fast-pace...
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GRC dashboard
GRC dashboard
Give your leadership, team, and wider business access to a customised view of your governance, risk and compliance performance.
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Mobile document navigator application
Mobile document navigator application
Your employees want to use the right information, not fight with duplicate forms, outdated spreadsheets and cluttered inboxes. Our document navigation application shows the right information to the right person, wherever they are.
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Accident & incident management software
Accident & incident management software
When an accident or incident occurs, it's important there is an accurate record of events to understand the root cause and prevent it from happening again. Use our accident and incident management software to properly record, communicate and identify trends to prevent it from happening again.
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Supplier management software
Supplier management software
Qualsys's supplier compliance management software provides you with all the controls you need to treat external providers as an extension of your business. Deliver unshakeable governance, risk and compliance controls, understand supply chain risks, and extend quality best practice to your suppliers....
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Computer system validation: The Qualsys approach
Computer systems that are used to support regulated processes in the pharmaceutical, healthcare and biological industry need to comply with the expectations of the regulatory authorities. One of the most crucial requirements is computer system validation. This is the umbrella term for ensuring all ...
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ISO 13485 software validation process
When you're implementing an electronic medical device quality management system, your software validation plan is of the utmost importance. You'll need to ensure that your system is working and continues to work as required.
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