DRUiD passes ISO 13485 Surveillance Audit.

In January 2025, DRUiD successfully passed its ISO 13485 surveillance audit—an essential milestone in our journey toward regulated diagnostic product development.

ISO 13485 is the internationally recognised standard for quality management systems in medical devices. Maintaining this certification ensures that our design and development processes remain compliant, rigorous, and ready for clinical translation.

With increasing regulatory focus on safety, traceability, and reliability, this certification builds trust with partners, clinicians, and end-users.

This milestone follows the progress of our UTI AMR diagnostic solution and supports our readiness for future clinical trials and market authorisation processes.

We continue to build not just novel technology—but a company rooted in quality.