Coffee and breakfast will be available.
See Veeva’s vision for incorporating AI, risk-based methods, and eSource into clinical data management. Learn how a biopharma builds efficiency and streamlines their data workflow.
Risk based data management (RBDM) – classifying, automating, and orchestrating critical data for proportionate review. What’s holding your team back from adopting risk-based approaches? How should KRIs drive the right actions in clinical data and clinical operations?
eSource – standardizing data collection across sponsors and sites. What have been your biggest barriers to scaling this in the past? If >10,000 sites adopted eSource, what would your team need to do or change for this to work?
See a deep-dive demo of CDB’s highest-impact features, and learn how to optimize workflows through hands-on training with Veeva Strategy and Services experts. Discuss real-world strategies to enhance oversight, automation, ingestion, and vendor communication with fellow CDB users.
Reconvene as a full group and discuss how to continue the conversation.
