
When registering medical devices in GreMDIS, the national registry of the National Organization for Medicines (EOF), companies must declare their regulatory role accurately. One of the most...

EUDAMED (European Database on Medical Devices) is no longer an optional pilot platform. Following the...

With the recent release of the ISO/IEC 27001:2022/Amd 1:2024 amendment , organizations managing an Information Security Management System (ISMS) are facing a...

If a company develops medical device software under Regulation (EU) 2017/745 (MDR), does the Cyber Resilience Act,...

For many growing tech companies, ISO 27001 certification feels like a major milestone, but also a major mountain to climb. That was exactly the situation facing AhoyAhoy...

At QC Analytics, we continuously improve our apps to align with Atlassian’s evolving platform and security requirements. As part of this commitment, we would like to inform our users about an...

We would like to inform all users that the QC Template Launcher app was successfully migrated from...

Managing content reviews and formal approvals in Confluence just got a whole lot easier! We’re excited to introduce...

We’ve recently made an important improvement to how we manage and publish our product documentation, even though the support site URL you know remains the same. Previously, our support documentation...

ISMS documentation requires easy access, speed, and reliability. Confluence Cloud can work as a Document Management System (DMS) aligned with ISO practice: all documents available, updated,...