Congratulations to the Unilever Oral Care team for a perfect ISO 13485 audit! Here's how they did it.
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.
Unilever's global operation demands fast, safe and efficient routes to market. Oral Care Quality Manager Paulo Ramos discusses how EQMS by Qualsys makes that possible for thousands of medical device products.