Case Study: Terumo achieves faster regulatory workflows with Essenvia

Terumo saves 20% of regulatory time with Essenvia

Terumo, a leading global medical device manufacturer, faced challenges managing over 40,000 regulatory artifacts across multiple non-validated systems, which limited information access and complicated workflows. They turned to the vendor Essenvia and its fit-for-purpose Medtech Regulatory Information Management System (RIMS) to centralize their data and simplify compliance processes.

By implementing Essenvia as a single source of truth, Terumo streamlined its regulatory workflows and established quick access to information, resulting in a 20% time savings. The Essenvia platform was implemented in 90 days and, with its flexible architecture, was quickly customized to match internal processes, leading to high user satisfaction and improved organizational visibility.

Terumo