Central data repositories and metadata-generated automation offer significant potential to increase efficiency in clinical analytics and accelerate drug development. However, many organisations are yet to fully harness the potential of these tools.
The session will incorporate:
Defining your automation objectives and assessing practical solutions - Presentation by Shafi Chowdhury
Demo of Metalytics metadata-driven clinical trial reporting tool
Q&A
About Metalytics
Metalytics helps pharmaceutical sponsors and CROs increase statistical programming efficiency, traceability, and quality with an intuitive clinical trial reporting application created by programmers, for programmers.
