eConsent Resources

  1. U.S. Renal Care Achieves 75% Site Adoption Of eConsent 5/1/2024

    By dispelling prevalent misconceptions regarding participant age, cost, and complexity, see how this platform emerged as a versatile, rapid, and effective solution tailored to the unique needs of the elderly renal care population.

  2. 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.

  3. 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.

  4. 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.

  5. 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.

  6. 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.

  7. Designing ePRO and eConsent Solutions that Participants and Sites Want 10/26/2022

    Participant-focused eClinical technologies offer significant potential to decrease paper-based processes and improve end-user experiences in collecting patient-reported outcomes (PRO) and informed consent, but many users continue to experience rigid technology, complicated hardware provisioning processes, and clunky implementations that leave sponsors, CROs and sites questioning the value. 

  8. 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.

  9. 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.

  10. Built For Sites To Benefit All 7/15/2024

    This one-minute video highlights the benefits of One Home for Sites. Join the movement to increase clinical trial capacity, because patients are waiting.