Case Study: Epredia achieves unified QA/RA and faster time-to-market with Veeva Systems' MedTech Suite

Epredia Transforms Quality and Regulatory Operations with the Veeva MedTech Suite

Epredia, a global leader in anatomical pathology formed in 2019 from PHC Group’s purchase of Thermo Fisher’s pathology business, set out to improve cancer diagnostics but faced fragmented quality and regulatory systems across six manufacturing sites. Disparate point solutions created complexity, inconsistency, compliance risk, and delays across the product lifecycle, so the company aimed to harmonize QA and RA processes on a single, scalable platform to reduce waste and boost efficiency.

Epredia selected the Veeva MedTech Suite and completed a six‑month rollout of Vault QualityDocs, Vault Training, and Vault RIM Submissions ahead of schedule and under budget. The cloud platform unified document control and training, enabled better tracking of regulatory submissions, simplified the IT landscape, and positioned the company for further Vault QMS and Registrations deployments—delivering streamlined QA/RA processes, reduced compliance risk, cost savings, and faster time to market.

Epredia

Mark Ramser

Senior Director of Global Quality