On November 17, Naru Intelligence, together with Ainhoa Ariceta Iturrioz and Maddi Arregi, taught the class Technical development of a medical device software of the second module on the Regulatory Framework.

Both of them currently work in the Regulatory Affairs and Quality Management department of Naru. Their work focuses on ensuring the safety and proper performance of the products developed and marketed by the company throughout their life cycle.

Naru Intelligence’s history as a manufacturer of healthcare software products dates back to its founding in 2017. Since its inception, the company has demonstrated an uncompromising commitment to regulatory compliance in its solutions. This inclination towards regulatory excellence is not only reflected in the participation in the Regulatory Expert Course, but also in the day-to-day running of the company.

Naru Intelligence stands out as a key player in the sector, not only for its technical expertise and knowledge in medical device development, but also for its ongoing commitment to the highest regulatory standards. This participation in the Regulatory Expert Course further reinforces Naru’s position as a reference in the field of healthcare regulation, highlighting its fundamental role in ensuring quality and safety in the medical device software industry.