eConsent Resources
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The Right EDC Solution For Oncology Trials
5/19/2023
Oncology clinical trials can be very complex, as are their data management needs. Understand why selecting the right EDC is crucial for managing them efficiently while providing compassionate care.
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How To Prepare An IRB Submission For A Remote eConsent Study
1/24/2022
IRBs are increasingly supportive of eConsent solution. Even so, researchers may find themselves in need of guidance as they prepare for an eConsent IRB review.
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Protocol Amendments And Electronic Consent: Overcoming The Challenges To Reap The Benefits
3/29/2022
Learn about some insights that have been gleaned from experience deploying eConsent on diverse trial types around the world.
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Sustainable Clinical Trials Through eClinical Innovation
8/26/2025
Clinical trials are essential to advancing medicine, yet they carry significant environmental costs. Inefficiencies not only drive emissions but also risk drug shortages and trial delays, and clinical technology solutions offer a pathway to more sustainable research.
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A Definitive Guide To Evidence Generation
10/18/2023
Obtain a complete understanding of enrollment, screening, consent, and data collection by diving into this introductory handbook on decentralized clinical trials.
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An Introduction To One Home for Sites™
4/18/2024
This on-demand webinar provides a thorough overview of why IQVIA Technologies is building One Home for Sites, how it works, and who should participate.
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eConsent Readiness In 24 Countries
3/12/2024
Discover how regulatory bodies worldwide, including the U.S. Food and Drug Administration and the European Medicines Agency, are now championing the shift towards eConsent adoption.
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How Capturing Data Directly Is Transforming Trials
2/3/2023
With the right eSource technology, discover how trial data can be aggregated, integrated, and classified to accelerate data analysis for insight-based decisions in real time.
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10 FAQs On eConsent
11/16/2023
Closely examine the challenges of adoption, integration, and compliance measures involving eConsent and gain valuable insights for those contemplating their incorporation in clinical trials.
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Biosample Tracking: A Consenting Dilemma
3/7/2023
Biosample collection is an inevitable part of most clinical trials. Learn how sponsors should be tracking every sample back to the source so as to not violate compliance issues.