This On Demand Solution Provider Webinar is brought to you by DIA in cooperation with

Creating adverse event narratives requires coordination between many parties within a pharmaceutical organization. Data managers and biostatisticians provide the data while medical writers and medical officers provide therapeutic area-specific guidance for content. Programming and validation are then required to tie all of this together. Given this complexity along with significant consequences for inaccuracies or delays, many organizations are seeking ways to streamline this process. This presentation will share industry experiences in meeting the challenge of automating the delivery of adverse event narratives for the clinical study report to medical writers.

Continuing Education Credits are not available for this event.