Webinar | November 2, 2018

Decisions For Your Next Trial: When To Adopt The CDISC Data Standard

Source: Cytel

New regulatory expectations are taking shape, including the need for interactive and transparent clinical data handling, increased safety data demands and electronic data (CDISC) submission. Trial sponsors must carefully plan their data consolidation and analysis strategies not only in preparation for CDISC-compliant submissions, but to respond to market influences and evolving clinical partnership models.