Case Study: OM Pharma scales global submissions with Veeva RIM

OM Pharma submits across 4 regions in 2 months with Veeva

OM Pharma, a Geneva-based biotech company, faced challenges with siloed regulatory information management systems that limited visibility into submission progress and created operational bottlenecks. Their reliance on multiple disconnected databases hindered workload forecasting and strategic planning. To address this, they turned to Veeva Systems for a solution using Veeva RIM, specifically Veeva Registrations and Veeva Submissions.

By implementing Veeva's unified RIM platform, OM Pharma harmonized its data and streamlined regulatory processes, creating a single source of truth. This provided the team with confidence in their data quality and improved governance. The solution enabled them to accelerate global submission preparation and delivery, successfully submitting to health authorities in Switzerland, Europe, and the USA within just two months of implementing Veeva Submissions Publishing. Veeva Systems provided the platform for OM Pharma to seamlessly scale across regions and navigate evolving global requirements.

OM Pharma