Corporations often try to unlock value by matching their structures to their strategies. Here's why an integrated qms is essential during a restructure.
Qualsys has helped over 400 businesses to be confident they are audit ready 24/7. Here are 15 lessons we’ve learned to prepare businesses for supplier, regulatory and certification body audits.
Here are three groups of people you'll come across when implementing EQMS and how to manage their expectations throughout the journey.
We asked our customers about the 3 top methodologies quality professionals should be applying. Here's what they said.
Every business strives to achieve a quality culture. Here's how EQMS is an essential tool for a culture of quality at Alliance Medical.
We've launched our new health check report and found our three strongest customer systems for the last month.
Whether it's a near-miss, critical incident or an employee displaying COVID-19 symptoms, your health and safety team need to know in seconds. Here's how.
Stewardship, data and governance initiatives that stick. Ian Brandon from the Good Governance Institute shares his insights from his work with the NHS.
How to fight for resources and recognition, and raise the profile of quality in an industry too focused on profit.
A culture of continuous improvement requires resilience, time & energy. It takes more than a single tool to achieve your quality goals. Here's our catalogue of services improve your quality culture.
Don't know your CTX from your CRISP? Access our acronym dictionary and slice through the quality jargon.
Meet Dan Moorewood, Qualsys' Implementation Analyst.
Here are 8 reasons your medical device company should ditch paper and invest in an electronic quality management system.
Common mistakes, best practice and audit tips. The Qualsys service team run through how to build a clean and compliant document stack to show your MHRA auditor.
We visited the Med-Tech Innovation Expo to hear about the future of the medical device industry. Here's what we learnt.
The FDA announced its intention to harmonise with ISO 13485 last year. That means 3 big changes to how medical device companies comply with CFR Part 820. We take a look at what the future holds.
How does EQMS help you to comply with FDA title 21 CFR Part 11? This article details exactly how and why EQMS helps you to comply.
02-09-20
18-02-20
01-07-20