EDC Resources
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eSource For A COVID Treatment Trial
1/17/2024
Unearth how this emerging biopharmaceutical company was able to overcome challenges to successfully facilitate a Phase 2 trial for a COVID-19 treatment in critically ill patients.
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Atlantic Research Group Builds Competitive Advantage With Medrio EDC
1/30/2023
By using Medrio’s EDC platform, learn how Atlantic Research Group was able to achieve the flexibility needed to span multiple therapeutic areas and eliminate redundancy in documentation.
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Data-Driven Physician Engagement For Ultra-Rare Diseases
2/3/2025
How can an effective partnership help you to utilize advanced data analytics to address the significant challenges of clinical trials centered around ultra-rare diseases?
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Comparing Patient And Practice Characteristics
10/24/2024
Explore research that suggests investments to expand the clinical research footprint among practices with low research engagement could help address persistent inequities in cancer clinical trial representation.
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Achieving Self Sufficiency In Data Collection For Optinose
2/12/2024
Uncover how this specialty pharmaceutical company was able to gain control over its EDC environment by adopting a solution their team could use in-house.
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How EHR-To-EDC Tech Can Streamline Study Data Acquisition, Management
7/23/2024
Recent assessments reveal that data verification, management, and monitoring account for over 25% of clinical research costs. See how Flatiron's Clinical Pipe, saves time and reduces costs.
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Industry Perspectives On Clinical Technologies
6/14/2023
Take note of the characteristics experts should consider when selecting an IRT provider, what sponsors are using more than one CTMS solution, the future of EDC, and more.
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The Next Steps To Modernize Clinical Trials With DHTs And AI
4/8/2025
Explore an innovative approach to seamless, real-time data capture through wearable sensors that aligns with the FDA's efforts to modernize trials through Digital Health Technologies (DHTs).
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FDA Guidance Has Implications For EDC And EHR eSource Capabilities
2/28/2023
Gain insight from an eSource study observing digitally received data as far back as 2007 to just before initial guidance was released by the U.S. FDA in 2013.
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From Paper To Digital Study Management In Large Patient Registries
2/13/2024
Uncover how this sponsor was able to independently design and oversee its clinical study, minimizing external assistance, and easing the workload for their sites through mobile app accessibility.