Making the transition from OHSAS 18001 to ISO 45001? Here's what you should focus on first.
Don't know your CTX from your CRISP? Access our acronym dictionary and slice through the quality jargon.
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 blitz your CE marking from Qualsys's services team.
A REACH-compliant chemical supply chain requires information transmission in both directions. Learn what you should be sharing here.
EPC-UK operates in one of the world's most dangerous industries. We asked the team how they use Qualsys's software solution to build unshakeable quality into their operation. Read the interview here.
Chemical companies working with hazardous substances must complete an SDS for REACH compliance. Business Development Manager Tom Hodgson explains what to do.
DYSIS Medical's Quality & Regulatory Manager Paul Houston shares his industry experiences and discusses the impact of Qualsys's software on his business.