30%–50% Faster Clinical Study Reports with Generative Artificial Intelligence-Powered Automation

Creating CSRs for regulatory submissions is a complex, time-consuming, and resource-intensive process. It requires input from multiple stakeholders and adherence to strict regulatory guidelines. Manual effort, data inconsistencies, and compliance risks often slow down submission timelines. In this paper, Axtria’s Clinical Solutions team lays out how a GenAI-enabled solution turns CSR delays into deliveries.

Key highlights:

• Accelerated Timelines: GenAI-powered automation reduces CSR authoring time by 30%–50%,  enhancing efficiency without compromising quality.
• High Accuracy and Compliance: Achieves over 90% accuracy  in interpreting clinical data while aligning with ICH-E3 guidelines.
• Simplified Collaboration: Intelligent workflows facilitate seamless coordination across geographically dispersed teams.
• Advanced Content Generation: Automates the creation of structured, scientifically precise narratives from complex clinical data sources.

Read this whitepaper to see how GenAI transforms CSR authoring, reducing costs and getting much-needed therapies to market faster.