Geo Resource Commitment
Discover how to guarantee system availability, even in worst-case scenarios. Learn how to recover in under 24 hours and minimize data loss with dedicated geo-redundant infrastructure.
Discover how to guarantee system availability, even in worst-case scenarios. Learn how to recover in under 24 hours and minimize data loss with dedicated geo-redundant infrastructure.
Most teams know something’s not working. This checklist helps you see exactly where and how much it’s actually costing you.
Scaling control across Europe
Operating in 21 European countries across 11 product categories, including licensed products, PXG pharma manages a complex and highly regulated packaging environment. As the portfolio expanded, the organization required a structured and scalable approach to artwork approvals, ensuring consistency, transparency, and regulatory control across markets.
From fragmented systems to compliance risk
Artwork approvals spanned multiple countries, product types, and external partners. Processes were managed across disconnected systems and manual touchpoints, limiting visibility and increasing coordination effort.
In a regulated pharmaceutical landscape, fragmented workflows don’t just slow teams down, they introduce compliance risk. PXG Pharma needed a harmonized framework that would standardize approvals, reduce errors, and create a clear governance structure across Europe.
A centralized artwork management framework built on WAVE
PXG Pharma implemented a centralized artwork management platform to streamline the full packaging lifecycle, from content approval through prepress sign-off.
Three structured workflows were introduced and embedded into daily operations as standard operating processes. These workflows established:
The new framework significantly reduced manual coordination and created a unified, Europe-wide approach to artwork approvals.
Standardized processes delivering measurable impact
With harmonized standard operation proccess-based workflows in place, PXG Pharma achieved:
The impact of these standardized workflows has been so significant that PXG Pharma is now moving forward with the development of a dedicated validated workflow, designed to replicate and formalize the same efficiency, control, and compliance benefits within a fully validated framework.
By transforming fragmented processes into a centralized and standardized system, PXG Pharma has strengthened governance, improved packaging quality, and created a scalable foundation for compliant growth across Europe.