Vanessa Buonavoglia

Master data is no longer a back-office concern, it is the backbone of operational excellence. This session explores how high-quality, trusted master data enables more accurate planning, optimised inventory levels, and seamless data flow across clinical supply systems.

Attendees will learn how adopting master data best practices can reduce risk, improve cross-functional alignment, and support compliance in a rapidly evolving regulatory environment. Through practical examples and proven approaches, this session will highlight the role of regular data audits, governance, and transparency in ensuring data integrity from study start-up through close-out.

When master data is right, downstream processes, from forecasting and packaging to distribution and reporting, perform with greater efficiency, confidence, and reliability. Join us to discover how investing in robust master data management can elevate clinical trial supply operations and future-proof your organisation.

Key Takeaways

t Learn how clean, standardised master data drives more accurate forecasts, reduces excess inventory, and minimizes supply risk. t Understand the importance of governance, routine audits, and transparency to maintain inspection-ready data across systems.

t Discover how trusted master data supports seamless integration between clinical, supply chain, and quality systems