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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Flexible By Design: Support For Early-Phase Oncology Trial
7/8/2026
Shifting cohorts, doses, and protocols challenge early-phase oncology trials. Learn how adaptable technology keeps studies on track.
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Re-Consent In Clinical Trials: Streamlining With eConsent
11/29/2023
Delve into a variety of triggers for initiating re-consent, perspectives of regulators and IRBs regarding the re-consent process, and the role of digital processes in preventing issues related to re-consent.
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Combining Patient-Centric Technology and RWD For Comprehensive Evidence
8/10/2022
Explore how by combining digital technologies with secondary RWD, researchers can gather a more holistic understanding of the patient.
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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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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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Addressing The Specific Complexities Of Oncology eCOA Clinical Trials
4/18/2022
What are the specific tools and keys to conduct eCOA trials in oncology successfully? This article identifies some of the relevant solutions to tackle oncology protocol complexities.
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How eConsent Primes Patients And Studies For Success
9/14/2022
Understand how the informed consent process ensures trial participants are adequately educated about the trial and what's required of them during the process while confirming their willingness to enroll.
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How Partnership Ensured A Successful First Digital Trial
5/1/2024
Discover how this collaborative approach and tailored recommendations led to the successful implementation of an eConsent tool for a kidney cancer study with U.S. Renal Care.
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Our Unified Platform Serves As eSource For COVID Treatment Trial
6/17/2024
Signant Biotech optimized technology for an emerging biopharmaceutical's Phase 2 COVID treatment trial in critically ill patients, minimizing paper data risks and streamlining consent and data management across multiple sites and solutions.