eConsent Resources
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The Win-Win Wth Virtual Visits – Better Experiences, Better Data
2/29/2024
Discover how researchers can design studies with the needs of the patient in mind to promote faster enrollment, high engagement, and the production of more complete and accurate data.
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eClinical Platform Accelerates COVID-19 Treatment Trial By 2 Weeks
1/8/2024
Examine a COVID-19 treatment trial that utilized integrated EDC, eConsent, eCOA, RTSM, and TeleVisit solutions, all within a single platform, to address three critical challenges.
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The New Era Of Evidence Generation In Clinical Trials
6/19/2024
Learn how top pharmaceutical companies are using novel innovations to drive greater speed, scale, and access in clinical research than ever before in this webinar hosted by Musaddiq Khan, Vice President of DCT Solutions at Medable.
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Right-Size Your eConsent Approach
11/17/2023
Delve into the art of tailoring the eConsent experience to match your study and patients' specific needs, such as crafting eConsent documents, selecting appropriate delivery models, and more.
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What Are Decentralized Clinical Trials (DCTs)?
8/23/2022
Discover how DCTs leverage “virtual” tools, such as telemedicine, sensory-based technologies, wearable medical devices, and direct delivery of study drugs and materials to patients’ homes.
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Tips For Tailoring eConsent For Optimal Patient Centricity
3/29/2022
While informed consent is a critical process for ensuring participant autonomy, consent forms are too long, unclear, difficult to read, and frequently exceed 9th grade reading levels. Explore why eConsent is a potential solution to this problem.
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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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Unleash The Power Of IQVIA Complete Consent
11/12/2024
Join Vinita Navadgi, and Amy Koller from IQVIA Complete Consent for an in-depth exploration of the eConsent landscape.
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Gradually Investing In Direct Data Capture Is Inevitable
2/2/2023
Given study decentralization and the many electronic sources of data now available, it is time for sponsors and contract research organizations to face the inevitable: EDCs need to be “sunsetted.”
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Navigating Successful eConsent Adoption From Sponsor To Site
10/17/2023
Drawing inspiration from real-world instances within the pharmaceutical and medical device sectors, watch as industry experts unravel the pivotal role of eConsent in optimizing modern clinical trials.