Accelerate compliant clinical trial reporting with open source
Clinical trial reporting is under pressure like never before. Timelines are shrinking, costs are rising, and compliance requirements are only getting stricter. This eBook reveals how top life sciences organizations are transforming reporting workflows with open source — achieving faster submissions, lowering costs, and ensuring FDA/EMA compliance.
• Accelerate submissions: Cut SDTM dataset creation time by up to 50%.
• Ensure compliance: Proven in FDA and EMA submissions with audit-ready workflows.
• Reduce costs: Lower licensing expenses with open-source standardization.
• Retain talent: Keep statisticians and data scientists engaged with the tools they prefer.
Why read this eBook
• Accelerate submissions: Cut SDTM dataset creation time by up to 50%.
• Ensure compliance: Proven in FDA and EMA submissions with audit-ready workflows.
• Reduce costs: Lower licensing expenses with open-source standardization.
• Retain talent: Keep statisticians and data scientists engaged with the tools they prefer.
