Abstract
With requests for real-time review and dynamic data visualizations, more study data is being generated than ever. Managing demands of sponsors and CROs, while balancing privacy & data security concerns, and navigating increasingly stringent compliance or regulatory requirements, adds complexity to modern study management.
We conducted 40 interviews with 57 individuals from sixteen global pharma and life-science organizations, based in eight different countries. Collecting 956 pieces of feedback, we curated the information into themes and used AI-tools to summarize the information.
Here we present study management challenges and current pain-points experienced within the R&D industry. Our research features worked examples, case studies and authentic user feedback. We discuss the evolution of the industry and growth predictions for 2025 (and beyond). We report how vendors need to be flexible to meet the complex requirements of a rapidly advancing market and discuss next-gen compatible solutions to ensure we enable the industry to discover new medicines, accelerate their timeframes and, ultimately, advance compounds to market safely.
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