Why are Clinical Data Standards Essential for EDC and Non-EDC Data?

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The current state of data standardization in pharma trials
Challenges in managing sponsor-driven standards and managing data manually
Using a clinical metadata repository (CMDR) to manage clinical data standards
Improving the collection of non-EDC data
Managing metadata for non-EDC data

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Maximizing value across drug development: Embracing a new CDMO and CRO partnership approach

In this webinar, we will present key insights from preliminary findings by the TUFTS Center for the Study of Drug Development, exploring how a comprehensive model that brings CDMO and CRO services under one roof can significantly impact the expected Net Present Value (eNPV) of drug development programs. We will demonstrate how streamlined services across drug substance, drug product, and clinical research can enhance efficiency, reduce timelines, and ultimately deliver high-quality therapies to patients faster. Key takeaways include:

Why are Clinical Data Standards Essential for EDC and Non-EDC Data?

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