Don Thampy, Head of Data Integration and Automation at Merck, discusses the evolution of RTSM from a functional tool to a strategic asset, highlighting how standardization and consolidated connections can overcome trial complexity.
Discover how a leading global biopharmaceutical company partnered with Veeva RTSM to replace manual workflows with a unified digital environment focused on an iterative design process, agile UAT execution and seamless data flows.
Gain invaluable insights from clinical researchers as they share the nuances of clinical supply challenges directly from the site level, including the added challenges of managing clinical supply for mobile sites.
Split into groups to discuss how we can best promote site centricity and improve overall supply accountability in clinical trial management.
A casual and informal time to continue conversations that were started earlier in the day.