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.
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.
It's time for quality managers to start selling quality properly. We spoke to Mark Eydman, Founder of Six Pillars Consulting, about how to do it.
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.
We dug into the ISO's recent survey report to see what's happened since ISO 45001 went live.
Still struggling with a manual, paper-heavy auditing programme?
Here's how things can get better.
Struggling to engage your workforce with health and safety? You need to start with the image problem.
Making the transition from OHSAS 18001 to ISO 45001? Here's what you should focus on first.
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.
Roy's Rules, the goo in the middle, and where compliance people go wrong. We interviewed Roy Snell about his book, The Accidental Compliance Professional.
We asked over 250 quality professionals to share their industry experiences, challenges and plans for 2019. This is what they said.
GRC professionals often neglect the most valuable measure they have. Learn what it is and how to track it.
Make your audit team a driver of continuous quality improvement with our 3 upskilling tips and some helpful resources.
W.E. Rawson have been using EQMS since 2016. Here's what they've achieved so far.
Our Head of Quality Assurance Kate Armitage celebrated World Quality Day with a live ISO 9001:2015 Q&A webinar session. Access the recording here.
Qualsys customer York Instruments have brought their revolutionary medical device one step closer to market with a flying-colours ISO 13485:2016 audit.
The circular economy is an increasingly powerful opportunity for businesses to boost efficiency, slice wastage and lighten their environmental footprint. Learn how to use EQMS for circular document, equipment and supplier management.
The Energy Savings Opportunity Scheme is now in Phase 2. Most businesses aren't taking full advantage of it. Here's why you should.
AG Barr's group quality manager shares his 3 tips for passing BRC audits with flying colours.
Economically motivated adulteration is an increasingly prevalent risk to your food supply chain. Learn which steps to take to protect yourself here.
The flexibility of Qualsys's software solution allows customers to apply their own ideas and initiatives. We asked Sirus Quality, Training & Health/Safety Manager Pauline Sourdille how she uses the system day-to-day.
Looking to bring a product to the European market? Read three tips to achieve CE marking from Qualsys's services team.