Real-World Data / Real-Word Evidence Resources
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Lessons From China And The United States On The Use Of RWE In Regulatory Submissions
9/3/2024
Read along as authors share their most significant lessons, offering guidance on how to harness the full potential of RWE to drive innovation and efficiency in drug development.
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Pitfalls And Possibilities: EHRs To RWD Via EDC
7/5/2023
Consider DIA GCP & QA Community Chair Terry Katz’s perspective on repurposing and analyzing EHR data for clinical research.
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How Medidata Link Is Supporting Moderna's Clinical Trial Real-World Data Linkage Initiatives
6/5/2024
Discover how Medidata Link empowers Moderna's clinical trial RWD linkage initiatives, enhancing insights into treatment outcomes while minimizing administrative burdens.
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Are You Using Real-World Evidence?
9/3/2024
This series of case studies illustrates how Real-World Evidence (RWE) can significantly enhance decision-making processes, leading to more efficient development strategies that save both time and costs.
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2024 MedTech Regulatory Updates: 4 Areas Of Interest
4/15/2024
In 2024, McKinsey's projections foresee a promising year for the MedTech industry, driven by innovation but shadowed by regulatory uncertainty.
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Enhancing Clinical Trials By Linking Them To RWD
5/16/2023
Learn how integrating participant trial data and real-world data into a standard EDC system can promote success in obtaining IRB approval.
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How Can Real-World Data Benefit Your Trials?
3/12/2024
Clinical trial data is being supplemented with real-world data (RWD) gathered from a variety of sources. Dive deeper into this emerging trend to understand its implications for the future of clinical research.
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Phase 4 Trials: A Critical Component Of Post-Marketing Insight
9/16/2024
Uncover how Phase 4 trials play an essential role in gathering additional real-world data on the treatment’s performance over a longer period of time and in more diverse patient populations.
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Patient Diversity Case Study: RWD Solutions
7/18/2022
See how by leveraging medical claims and diversity data, this clinical trial sponsor was able to identify relevant patients meeting the trial’s I/E criteria, broken out by race and gender.
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Benefits Of Delegating Your Oncology Trials Patient Screening Process
10/16/2024
Explore the integration of Electronic Health Records (EHR) into oncology clinical trials, highlighting both challenges and potential advancements.