Connected Data Flow and Standards: A data management approach combining standards, technology and data flow to accelerate FSP clinical development
*** Friday, June 11, 2021 at 11am EDT *** Data plays a central role within drug discovery and as decentralized trials become more prevalent in the industry, the need to process and engage with enterprise level solutions and the integration of technology to map data to standards become a must. As the central conduit to this IQVIA data management will share the importance of how systemic compliance to standards together with a central data strategy can accelerate clinical development across an organization through an innovative FSP approach.***On demand available after final airing until June 11, 2022***
- Highlight how standards, technology and data flow can work together to accelerate your clinical development processes through an FSP solution
- Discuss the importance of true adoption and compliance enabling connectivity towards a push-button study setup (eCRFs through TLFs and DMP)
- Discuss the possibilities of a holistic approach to data cleanliness through centralized data review and issue management. (Case study E2E example)
- Realize the importance of systematic compliance to standards and the full impact of deviations from those standards
- Understand how the systems interact (MDR/CDR/workflow tool) to optimize the automation of digitized processes
- Establish the importance of synergetic enterprise level solutions versus disparate transactional solutions
- Discover how connected data flow and standards improve overall study quality, and operational efficiency, leading to improved patient safety.
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