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.