In this free webinar, learn about the benefits of executing a centralized monitoring strategy from a global clinical operations expert. Attendees will gain insights into source data review (SDR) and source data verification (SDV) sampling strategies, and the limitations of using a traditional monitoring approach.
TORONTO, April 23, 2025 /PRNewswire-PRWeb/ -- Traditional monitoring strategies, such as source data review (SDR) and source data verification (SDV), have long been the cornerstone of ensuring clinical trial data quality.
While effective in the past, these methods are resource-intensive, costly, and do little to improve data quality. With advancements in technology and data analytics, centralized monitoring has emerged as a key contributor to monitoring, allowing for significantly reduced SDR and SDV sampling strategies.
Centralized monitoring, a key component of risk-based quality management (RBQM), offers a broader and more comprehensive view of trial data, enabling faster deviation identification and reducing monitoring costs by up to 20 percent. Despite its potential to optimize clinical trials significantly, the industry has been slow to adopt centralized monitoring and shift away from traditional approaches like SDR and SDV.
The expert speaker will examine the limitations of traditional methods, the benefits of transitioning to centralized monitoring and why this innovative approach should become the new standard for driving clinical trial excellence.
Register for this insightful webinar to explore the evolution of monitoring strategies in clinical research.
Join Nicole Stansbury, Senior Vice President, Global Clinical Operations, Premier Research, for the live webinar on Tuesday, May 13, 2025, at 11am EDT (5pm CEST/EU-Central).
For more information, or to register for this event, visit Breaking Free from SDR and SDV: The Case for Centralized Monitoring.
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