eConsent Resources

1. Bridging Clinical Efficacy And Real-World Effectiveness In Digital Therapeutics Trials 2/7/2022

   No matter how conclusive clinical evidence is for medical treatments, developers may struggle to see precisely how their treatment performs in the real world—outside the controlled environment of the clinic or office.

2. Why Now Is The Right Time To Adopt eConsent 12/19/2023

   As much as eConsent helps staff, participants are also likely to prefer it over traditional paper methods. Explore the benefits of eConsent and some strategic steps sites can take right now to adopt the process.

3. Evidence And Insights: Analysis On The Power Of Digital Trials 5/29/2024

   Digital and DCT elements like eCOA, platforms, and wearables have transformed the ways we conduct clinical research. Read through the latest industry analysis and data on the real impacts these technologies have on clinical trials with this new ebook.

4. Why eSource: The Advantages of Abandoning Paper Records 2/16/2023

   Eliminate transcription errors and fully leverage supporting eClinical technology to provide a reliable consistent exchange of information.

5. Linking Clinical Trial Data With Real-World Data: Q&A With HealthVerity 5/16/2023

   Director of Partners and Alliance Management at HealthVerity KC Ahlberg discusses some key trends related to the use of real-world data in clinical trials, and the value sponsors are realizing through data linkage.

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. Better eConsent Through Education Best Practices 9/23/2022

   eConsent can have a positive impact on participant retention, but learn why that is only part of the challenge of meeting participant needs in a clinical trial.

8. Headed Down Registry Road? Here Are The EDC Features You'll Need 3/18/2022

   Most of us rely on electronic data capture (EDC) to help us reach our study destination. How do we choose the EDC "vehicle" that will get us there safely, with minimal delays? Consider the relative importance of these key EDC features.

9. Work Flow Walk Through: eConsent Platform 2/28/2023

   Within DSG’s unified system, e-consent is simple. Witness how teams can easily and efficiently register participants for clinical trials.

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.