Webinar
Accelerating CSR Timelines: Applying Real-Time Data, Governed Standards and Expert Oversight
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Pharmaceutical sponsors are under increasing pressure to reduce the time from database lock to clinical study report (CSR) while maintaining data quality and regulatory compliance. This webinar will demonstrate how pharma organizations can apply technologies and standards to streamline data flow, eliminate rework, and accelerate submission timelines. Attendees will learn how real-time data analysis, governed by CDISC standards and automation, can convert traditional workflows into scalable, high-quality processes that enable faster and more robust delivery of CSRs while ensuring high standards.

The session will feature the practical application of Data Science technologies and the critical role of data standards engineers in aligning protocols with CDASH, SDTM, and ADaM from the outset. These experts provide strategic and tactical oversight across the data lifecycle, helping biostatistics, data management, and clinical operations teams harmonize standards, adapt to evolving trial designs, and ensure submission-ready outputs. Real-world use case will illustrate how IQVIA are reducing cycle times from weeks to days while improving compliance and operational efficiency.

Participants will also gain actionable insights into how centralized standards repositories, consumption governance, and tech-enabled automation can deliver long-term value across portfolios. Whether you are leading statistical programming, managing data operations, or overseeing trial delivery, this session will equip you with an understanding of the tools and strategies we are using to operationalize governed standards and DSSM technologies for measurable impact.

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