Accurate clinical studies rely on accurate safety data reviews – and software plays a crucial role in facilitating the analysis and reporting processes involved in clinical trials.
In this webcast, you'll learn more about how to simplify your data analysis and consolidate workflows in clinical trials by providing interactive reviews for medical monitors, reviewers and writers.
This randomized controlled trial case study will show how to:
- use review templates, study population filters and interactive drill downs to answer a medical line-of-question analysis.
- generate complete patient profiles and adverse event narratives.
- streamline the reporting process for CDISC data standards in accordance with regulatory guidelines.