Pharmaceutical manufacturing environments are increasingly reliant on the seamless integration of physical assets and digital systems to support data-driven decision-making. This session explores how production facilities can establish unified data pipelines across equipment, systems, and processes. Emphasis will be placed on practical methodologies for aggregating operational and contextual data, applying analytics for process improvement, and aligning digital infrastructure with quality and compliance requirements. Through applied use cases and cross-functional insights, attendees will examine how integrated data strategies contribute to more reliable, efficient, and compliant operations. In this session, you will learn how to:

• Integrate and contextualize data across equipment, systems, and digital platforms to enable unified process oversight.
• Apply analytics techniques to support decision-making, enhance process visibility, and detect inefficiencies.
• Align digital infrastructure and data usage with regulatory and quality system requirements in GMP environments.