At Ardra Lab, our team developed the intelligent application software behind a next-generation eye-retina diagnostic robot, delivering highly reliable, software-driven retinal diagnostics with medical-grade accuracy within a Month. This project reflects our strength in building end-to-end vision systems that combine precision engineering with real clinical usability.
We engineered advanced calibration and triangulation algorithms to achieve vision-based precision, enabling the robot to localize with ultra-fine 0.1 mm accuracy without physical markers—well beyond typical imaging limits. This breakthrough reduced setup complexity while dramatically improving diagnostic reliability.
To ensure the solution was ready for real-world clinical environments, we designed a clean, clinician-friendly interface and implemented seamless triple-camera synchronization, ensuring consistent imaging and an intuitive workflow for healthcare professionals.
At Ardra Lab, we engineer medical and healthcare technology with compliance so your product isn’t just functional, it’s certification-ready.
Our development process is designed to align with globally recognized standards and regulatory expectations, including
ISO 13485 (Quality Management for Medical Devices),
ISO 14971 (Risk Management),
IEC 62304 (Medical Device Software Lifecycle),
IEC 60601-1 (Safety & Essential Performance), and
IEC 62366-1 (Usability Engineering). We also support regulatory deliverables and documentation frameworks required for
21 CFR, (electronic records/signatures), and
EU MDR readiness. For data-driven and connected products, we incorporate privacy and security best practices aligned with
HIPAA, GDPR, and secure-by-design principles, ensuring your solution can confidently move from prototype to clinical-grade deployment with audit-ready documentation and engineering rigor.
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