Decentralized Trial Technology Resources

1. The Promise Of IQVIA One Home For Sites: A Site CEO's Perspective 2/28/2025

   By providing research sites with a unified, streamlined interface, we can reduce operational friction, enhance collaboration, and ultimately accelerate the development of new therapies.

2. Beyond Integration: Flexible Orchestration Of IRT And eCOA Solutions 4/25/2023

   Consider how integrated response technologies and electronic clinical outcomes assessments can improve configurability, study start-up, and flexible mid-study changes.

3. The Rise Of Decentralized Clinical Trials 3/29/2022

   Discover how technological advancements have created the Internet of Things (IoT), in which numerous devices, including wearables like fitness trackers, can all be connected through software and cloud computing. 

4. What Universalized Terminology Means For Decentralized Research 10/26/2022

   Many DCT stakeholders have attempted to release terminology guides as it relates to their own dealings, however, there had never been a wide range of universalized DCT terms until now. 

5. Deconstructing Central Rating In Clinical Trials 1/27/2025

   Analyze several commonly held misconceptions about Central Rating and its ability to ensure data validity and study success in this

6. Regulatory Opportunities For Decentralized Clinical Trials: Insights From The SHASTA Project 5/13/2025

   Project SHASTA, a pioneering effort to measure the benefits of decentralized trial elements, reveals significant regulatory opportunities that could shape the future of clinical research.

7. 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.

8. How eConsent Can Help Legally Authorized Representatives 6/22/2022

   Software vendors often forget to think about the needs of LARs, even though they play a vital role in clinical trials. Explore three ways eConsent can help LARs complete the informed consent process.

9. How To Use Real World Data To Maximize Patient Recruitment In DCTs 2/7/2022

   In the clinical trial space, RWD helps support research design, protocol and patient engagement goals. Perhaps the most immediate way clinical research leaders can harness the power of RWD is as a tool for optimized patient recruitment. Learn how this can be done in the available blog.

10. Taming The Complex Clinical-Trial Ecosystem 4/9/2025

    To navigate the growing number of vendor portals required for clinical trials, sites are seeking a vendor- and sponsor-agnostic solution to enable single sign-on and study organization.