We are pleased to announce that our company has successfully completed the Stage I audit under the EU Medical Device Regulation (MDR).
During the audit, our quality management system, regulatory framework, and documentation readiness were systematically reviewed, with positive outcomes and constructive feedback from the auditing body.
The successful completion of the MDR Stage I audit represents an important milestone in our ongoing compliance journey with EU regulatory requirements. We will continue to strengthen our systems and preparations in anticipation of the next audit stage, ensuring sustained compliance and high-quality standards.
