Our Research and Development department is the beating heart of innovation, as this area is entirely dedicated to expanding and perfecting our Clinical Chemistry diagnostic products. The consolidated experience of our scientific and technical staff guarantees not only the satisfaction of every application and analytical request, but also proactivity in the development of new generation reagents and IVD kits.

We are committed to providing solutions that exceed current standards, improving the sensitivity, specificity and on-board stability of our products. Each new test is developed following rigorous Design Control to ensure that analytical performance translates into tangible clinical benefits for the patient.

Rigour and reliability are essential pillars. Thanks to a Quality Management System (QMS) implemented and certified according to ISO 13485, we scrupulously monitor the entire supply chain: Controlled Production: From the selection of raw materials to the filling of batches, we ensure maximum traceability and reproducibility.

Product Quality Control (QC): Each batch of reagents undergoes rigorous testing to ensure analytical performance and stability before being released onto the market. IVDR Compliance: All our devices comply with Regulation (EU) 2017/746 (IVDR). This commitment ensures that our clinical laboratory customers receive safe, reliable devices that are validated to the highest European standards.