The DIR collects and analyses real-world implant treatment data over time to support patient safety, quality assurance, and evidence-based clinical practice.

By contributing to a broader dataset, clinicians help identify trends, outcomes, and potential risks that can inform treatment decisions and improve consistency of care.

No. Participation is voluntary and designed to complement existing clinical record-keeping systems.

The DIR operates under an ethics-approved opt-out model. Patients are informed about the registry and can choose not to participate at any time.

Data is used in a de-identified and aggregated format for ethically approved research, monitoring outcomes, and supporting continuous improvement in implant dentistry.