DIA 2018 Global Annual Meeting

Component Type: Session
Level: Intermediate
CE: ACPE 1.00 Knowledge UAN: 0286-0000-18-658-L04-P; CME 1.00; IACET 1.00; RN 1.00

Historically, the clinical document writing process is error prone due to human error and its use of old technology, which does not integrate well with all the systems used in clinical trials. By automating and integrating clinical authoring, we improve both accuracy and efficiency, and leverage information across clinical business systems. The result is higher overall quality and consistency, more timely document authoring, and rapid knowledge sharing across departments. This session will describe how various companies have solved this problem. One solution was to create a cloud-based software solution for authoring, reviewing, and approving clinical trial documents. The Collaborative Authoring Tool (CAT) integrates many downstream systems to automate the transfer of content and enables the re-use of standard language to improve quality and consistency

Learning Objectives

Describe custom software that facilitates the collaborative authoring, reviewing, and approval of clinical documents.

Chair

David Twomey

Speaker

CASE Study: Collaborative Protocol Authoring with Tech-Enabled CPT and Reuse
Mitzi Allred, PhD