Case Study: Canterbury Scientific streamlines compliance and quality processes with Greenlight Guru

Canterbury Scientific cuts audit time from 4 days to 2 with Greenlight Guru

Canterbury Scientific, a New Zealand-based IVD manufacturer with a global footprint, faced significant inefficiencies with its paper-based quality management system. Managing numerous SOPs and work instructions across multiple regulatory jurisdictions (including FDA and EU MDR/IVDR) led to frustrating delays in document control, change management, and audit readiness. Seeking a modern, scalable solution, the company selected the medical-device-specific eQMS from Greenlight Guru.

Greenlight Guru provided a streamlined, cloud-based platform that automated quality events and document control. The implementation led to immediate time savings, with audit preparation shrinking from six weeks to a much shorter period. Notably, a recent four-day customer audit was completed in just two days. Internal audits are now consistently completed on time, and daily quality processes are more efficient with automated tracking. Canterbury Scientific credits Greenlight Guru with creating a compliant foundation for global operations and highly recommends it to other IVD companies.

Canterbury Scientific