EDC Resources
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Real-Time Trials Need Real-Time Data You Can Trust
7/30/2026
The FDA just kicked off real-time clinical trials with AstraZeneca and Amgen. But speed means nothing if the underlying data is inconsistent.
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Clinical Data Workbenches: A Buyer's Guide
6/21/2024
Learn to effectively evaluate and select the ideal clinical data workbench that best suits your organization's specific operational and strategic objectives with our comprehensive guide.
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Emerging Biopharm Rapidly Sets Up Phase 1 Oncology Trial
1/16/2024
Uncover how an emerging biopharmaceutical company was able to expedite the initiation of a Phase 1 oncology trial for a novel treatment targeting relapsed/refractory multiple myeloma.
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Executing Decentralized Clinical Trials More Smoothly
11/17/2023
Seize the opportunity to elevate your approach to DCTs by watching this presentation on the importance of adopting a fully unified EDC/CDMS to alleviate the burdens on users, sites, and patients.
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CRF Validation Best Practices: Building Reliable Clinical Trial Databases
6/29/2026
CRF validation improves data quality and efficiency. Early planning, clear edit checks, and balance reduce rework, ease site burden, and enable more reliable, streamlined study execution.
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Visual Analytics And Discovery Platform For Scientific And Clinical R&D
8/18/2021
A pharmaceutical company was looking to deploy a software solution for a small R&D group. See how an enterprise-class visualization and analytics platform enabled maximized understanding of research data.
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End-To-End Clinical Data Flow
6/24/2024
Explore the interconnected data flow across Veeva Vault EDC, Veeva CDB, Veeva RTSM, and Veeva ePRO to visualize how these products work together seamlessly.
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Vault Safety-EDC Connection
6/24/2024
Learn how to automate the flow of Serious Adverse Event (SAE) information between data management and safety systems, enabling more timely responses by Pharmacovigilance (PV) teams.
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Unlocking Scalability In Pharma With AI
10/18/2023
Uncover how artificial intelligence and machine learning could emerge as the most pivotal technologies of our era, with the potential to facilitate scalability in pharmaceuticals and other industries.
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The Significance Of Quality Data In Meeting FDA Regulatory Scrutiny
6/19/2023
Data Science expert Rod McGlashing explains how scrutiny from the FDA spurs regulatory compliance, resulting in better data quality and the creation of optimal applications for intellectual property.