To register their devices in India, a Switzerland-based leading innovator of devices for dental use approached Freyr to provide Regulatory services. The devices in scope were manufactured at different sites and were a mix of diversified device categories falling under different classification rules, thus making the grouping into a single application challenging. However, Freyr acted as an Indian Authorized Agent (IAA) and provided support for all the Regulatory requirements, starting from decoding accurate classification and gap analysis to successful device registration and acting as an Indian Authorized Agent (IAA).

Read the proven case to know, how Freyr overcame the challenges during the CDSCO registration process in a timely manner.