eConsent Resources

  1. The Building Blocks Of DCT: How To Create A Seamless Experience Across eConsent, eCOA, And More 3/29/2022

    With more than 76% of sponsors seeking to implement decentralized solutions this year, there’s never been more attention given to decentralized trials. Discover why decentralized trials must take a unified approach, one that alleviates burdens for patients and sites in order to drive cost savings and realize efficiencies. 

  2. 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.

  3. Medrio eConsent 10/25/2023

    Support the digitization of the participant consent process and begin creating multimedia-enhanced electronic informed consent forms (eICFs) that participants sign electronically, eliminating burdensome and error-prone paper-based processes.

  4. Driving Customer Profitability With Enterprise Platform, Pricing 2/29/2024

    Explore how the solutions and approaches offered by CDS can help different research stakeholders conduct more cost-efficient clinical trials in the industry's pharmaceutical, biotech, and device sectors.

  5. Waiver Of Consent vs Waiver Of Written Consent 11/21/2024

    Learn the distinctions between a Waiver of Consent and a Waiver of Written Consent in clinical trials, and the importance of informed consent, particularly in the context of virtual trials.

  6. EU Annex 11: How To Stay Compliant 11/16/2022

    EU Annex 11 lays out the European Union’s regulations for using computerized systems during clinical trials. Learn how sponsors and sites seeking treatment approval in the EU must follow Annex 11. 

  7. 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. 

  8. 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.

  9. Unlocking The Power Of Real-World Evidence In FDA Submissions 5/15/2023

    Understand the gaps between how data is collected in real-world evidence (RWE) and randomized clinical trials (RCT) and how RWE is quickly finding ways to catch up.

  10. EDC For Mid-Study Changes In Medical Device Clinical Trials 6/21/2022

    In this case study, discover how a company was pointed to an electronic data capture (EDC) system that was quick to adapt and easy to scale as the study changed.