Accelerating Technology Transfer Through Unified Recipe Management And Modern Platform Architecture

This webinar session addresses a critical challenge in pharmaceutical manufacturing: the lengthy technology transfer times associated with bringing new drugs to production facilities. The session will demonstrate how a unified recipe authoring workflow can dramatically reduce these technology transfer timelines while enhancing validation efficiency. By consolidating traditionally separate systems—Manufacturing Execution Systems (MES), batch control, and process control—into a single, integrated platform, pharmaceutical manufacturers can eliminate redundant steps and reduce opportunities for errors. We will explore how this architectural transformation delivers multiple benefits and how modern containerization techniques enable agile delivery of new functionality without impacting the validation status of existing application components.

By deploying new features without requiring fundamental platform version changes, manufacturers can reduce validation overhead and accelerate the time-to-market for new pharmaceutical products. Explore real-world examples of how this unified approach effectively tackled the inefficiencies of siloed systems and showcased improved operational efficiency.