Focused ISO 13485 Audit Completed – Reinforcing Quality at DRUiD

DRUiD has successfully completed a focused audit to ISO 13485, the international standard for quality management systems in medical devices.

This audit examined specific aspects of our development and quality processes, ensuring they meet the rigorous requirements expected of regulated diagnostic products.

The outcome reinforces that our internal systems, documentation, and design controls are aligned with the standards necessary for future clinical validation and eventual market approval.

Focused audits like this are a key part of building a culture of continuous quality, especially as we transition from early-stage development into technical verification, manufacturing readiness, and clinical studies.

We remain committed to upholding the highest standards of quality, safety, and performance across all aspects of our work—from product design to patient impact.