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Xtalks, Online
2025-04-30
Clinical data quality is not the sole responsibility of any one function—it is a shared commitment that begins well before the first patient is enrolled. So why is risk-based quality management (RBQM) still often viewed as a monitoring-only exercise?
One key reason may be that many RBQM implementations fall short due to fragmented data sources, limited real-time access and a lack of advanced tools to proactively identify and manage risk.
In this webinar, the expert speakers will introduce a more integrated approach—positioning RBQM as the connective tissue of clinical operations.
By breaking down silos and embedding data quality oversight throughout the trial lifecycle, RBQM can become a powerful enabler of both compliance and efficiency. The key topics will include the following:
A Holistic View of RBQM: Understand how RBQM can be more than just monitoring—it can be a strategic framework integrated across the entire trial process
Common Barriers to Effective RBQM: Explore how the absence of a single source of truth, real-time data access and advanced analytics limits risk detection and decision-making
RBQM as a Collaboration Catalyst: Learn how RBQM can foster cross-functional alignment, streamline oversight and support continuous data quality from startup to closeout
Register for this webinar today to discover how a modern, integrated approach to risk-based quality management can transform from a monitoring task into a strategic driver of clinical trial success.
Keywords: CRO, Risk Management, Clinical Data, Regulatory, Data Management, Clinical Data Management, Risk-Based Quality Management, Patient Management, RBQM, Quality
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Organized by:
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Xtalks |
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Invited Speakers:
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Olgica Klindworth, VP, Data Quality and Risk Management Solutions, Medidata
Anne Rosenberg, Solution Services Principal, Data Quality and Risk Surveillance, Medidata
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Deadline for Abstracts:
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2025-04-30
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Registration:
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Free Registration
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E-mail:
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tristan@xtalks.com
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