eConsent Resources
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Designed To Help Sites Increase Clinical Trial Capacity
7/25/2025
IQVIA One Home for Sites is a platform that serves as a neutral aggregator, connector, and communicator of the key systems and tasks a clinical research site needs to perform across all the trials it is conducting.
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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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The Revival Of Electronic Informed Consent
11/2/2022
The clinical research industry has been reluctant to adopt eConsent for several reasons. Unearth how the industry should continue exploring and implementing digital technologies in earnest in the future.
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Headed Down Registry Road? Here Are The EDC Features You'll Need
3/18/2022
Most of us rely on electronic data capture (EDC) to help us reach our study destination. How do we choose the EDC "vehicle" that will get us there safely, with minimal delays? Consider the relative importance of these key EDC features.
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Oncology Preferences From Patients And Caregivers On Trial Tech
6/14/2023
Delve into the preferences of patients and caregivers in the field of oncology, specifically regarding eConsent, telehealth, wearables, and other digital technologies.
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Simplify Clinical Trial Technology With An Emerging Aggregation Platform
7/24/2024
Sites are frequently overwhelmed with the sheer number of technologies they must work with to conduct a clinical trial, and this aggregation platform can streamline trial management.
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Evidence And Insights: Analysis On The Power Of Digital Trials
5/29/2024
Digital and DCT elements like eCOA, platforms, and wearables have transformed the ways we conduct clinical research. Read through the latest industry analysis and data on the real impacts these technologies have on clinical trials with this new ebook.
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Essity Uses eConsent To Optimize Enrollment
8/15/2023
See how a global hygiene and health company was able to deploy virtual methods through a strategic partnership to recruit and retain participants, streamline consent, and analyze patient data.
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Successful Subject Creation With eCOA, eConsent, & IRT Process Flow
5/26/2023
Watch a short walkthrough of how IRT and electronic Clinical Outcome Assessment (eCOA) solution on a unified platform delivery drives smoother study orchestration.
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Bridging Clinical Efficacy And Real-World Effectiveness In Digital Therapeutics Trials
2/7/2022
No matter how conclusive clinical evidence is for medical treatments, developers may struggle to see precisely how their treatment performs in the real world—outside the controlled environment of the clinic or office.