With their offerings spanning diabetes, oncology, obesity therapies, and beyond across facilities worldwide, a global leader in pharmaceutical manufacturing faced a growing tension between its operational ambitions and the integration infrastructure holding it back.
The company’s equipment integration layer was built on a custom .NET architecture, with bespoke C# DLLs managing data flows between manufacturing equipment and critical business systems like MES, recipe databases, and reporting platforms.
For a time, it worked. But as integration needs expanded across the global manufacturing network, the limits of the legacy model became impossible to ignore.
Every integration change — a new MES interface, a recipe data flow adjustment, a reporting feed update — required a full development cycle. There was no way to configure; only to code. That distinction created friction at every level:
For a regulated manufacturer where data integrity and audit control are non-negotiable, this wasn’t a technology preference issue. It was an operational and compliance imperative.
The full scope of how Orise designed, deployed, and validated this solution, including the specific architecture decisions, integration approach, and qualification strategy, is detailed in the full case study.
The impact was tangible across five dimensions:
The full case study details the six-phase implementation roadmap, the specific platform components involved, and the governance framework that made it work in a regulated environment.
Want to explore what a similar modernization could look like for your organization? Schedule a conversation with the Orise team.