eConsent Resources

  1. 3 Proven eConsent Implementation And Adoption Best Practices 1/19/2024

    By advocating these three essential best practices, learn how stakeholders can navigate the complexities of eConsent adoption with confidence and enhance the overall efficiency and success of clinical trials.

  2. 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.

  3. How eConsent Delivers Value For Sponsors 9/21/2023

    Delve into the data substantiating experiences with electronic informed consent to better understand their positive impact on the outcomes of clinical trials.

  4. The Impact Of An AI Enabled Consent Process 5/15/2024

    In this episode of Download with Derk, we take an in-depth look at our internal experiment where Castor Companion was utilized during the consent process.

  5. eConsent – The Enrollment Solution For Decentralized Trials 2/1/2022

    The COVID-19 pandemic and the increased technological competence required to enroll and retain research participants has left many organizations wondering how to modernize their enrollment and consent process. Find out more about the landscape and its impact in the available webinar.

  6. 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. 

  7. Hybrid eConsent For On-Site Or Remote Patient Enrollment 8/11/2022

    Castor’s suite of modular eConsent solutions creates clinical trial efficiencies from recruitment and screening, all the way to direct data capture and analysis. 

  8. 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.

  9. Introducing Digitally-Enabled Biosample Consent Storage 6/13/2024

    Despite the rise of digital solutions in healthcare, paper consent forms are still common in today’s clinical trials. Unfortunately, these paper forms pose significant challenges in retaining the documentation of informed consent for centrally stored biospecimens.

  10. Preparing Studies With eConsent For IRB Approval 6/7/2023

    Understand how eConsent can benefit trials and align with IRB ethical commitments, how to prepare your IRB submission for approval, and the future impact of large language models.