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Unlocking the Potential of Metadata in Clinical Trials Driving Transparency and Efficiency 1 месяц назад


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Unlocking the Potential of Metadata in Clinical Trials Driving Transparency and Efficiency

Overview: Over the years, pharmaceutical companies have made significant investments in submission-related data. However, untapped potential lies in the metadata surrounding these outputs, which offers opportunities to enhance trial operations. This webinar delves into the intricate ecosystem that underpins clinical trials, spotlighting one node in this network, its interconnected components and their upstream and downstream functions. We’ll also propose a novel approach to achieving transparency across the entire trial lifecycle, paving the way for insight-driven technology investments eliminating the guesswork around the success of new initiatives. Key topics to be covered include: • The Trial Lifecycle Ecosystem: Understanding the web of functions, processes, and handoffs. • Metadata Beyond Submissions: Exploring biospecimen metadata as a pivotal example. • End-to-End Visibility: Identifying targets to improve operational efficiency. • Enabling Emerging Technologies: Laying the groundwork for impactful technological advancements. Join us to explore how your non-submission data can drive operational efficiency and transparency across the clinical trial lifecycle.

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