Webinar | October 10, 2023

Technology Overload: Addressing The Site And Sponsor Challenges Of Digital Trials

Source: Medable

While clinical trials have made significant strides in their digital transformation, the multitude of emerging technologies can be overwhelming for investigative sites. Running a single clinical trial often requires the use of up to 15 different systems (such as EDC, EHR/EMR, payment processing, CTMS, radiology, and various technology vendors), in addition to the need to adapt to remote site staff and virtual facilities. While technology should, in theory, simplify site operations, the abundance of disparate solutions can actually create additional challenges.

In this webcast, the following speakers will delve into the site's perspective and emphasize the importance of implementing a change management strategy, complemented by a unified digital trial platform:

  • Andrew Mackinnon
  • Annie Hesslewood
  • Katie Madden
  • Nathan Morton

Specifically, the presenters will delve into how this platform can seamlessly integrate eConsent, eCOA, sensor data, and workflow integration into a cohesive end-to-end experience. Such an approach ensures that sites can operate efficiently, allowing them to concentrate on the well-being of trial participants.

Additional key learning objectives include:

  1. Identify common challenges faced by sites in the realm of digital trials, including issues related to flexibility, autonomy, and budget constraints.
  2. Gain insights into guidelines for selecting and combining the most suitable technologies for investigative sites.
  3. Explore effective change management strategies to help sites embrace and become proficient with new technologies.
  4. Examine a real-life case study illustrating successful implementation of digital trial solutions aimed at maximizing site productivity.
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