EDC vs eSource: Is it Time to Move?, Upcoming Webinar Hosted by Xtalks

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In this webinar, industry experts will explore some of the most pressing questions in the clinical trial industry: is eSource better than Electronic Data Capture (EDC)? How can a clinical research associate perform source data verification when the data are eSource? When should EDC or eSource be implemented? Is it possible to take on a hybrid approach? Join this free webinar to get the answers you are looking for.

Xtalks Life Science Webinars

Listeners should leave the webinar with a solid understanding of the challenges that they would face if they were to adopt eSource for their next clinical trial and also an idea of how eSource will be used in the future.

More and more clinical trials are using eSource as a way to avoid data collection delays and monitoring costs. But for some sponsors, the step up from Electronic Data Capture (EDC) creates challenges for their existing processes and legacy technology platforms.

eSource is a solution that provides real-time data collection and access which can cut huge amounts of time and effort in the trial process, for example, by reducing site visits by Clinical Research Associates (CRAs) for source data verification. But there are challenges in the adoption of eSource such as the practical problems of scaling across many different sites and geographies, technology barriers and costs of change management.

Join an informative live webinar on Wednesday, February 26, 2020 at 11am EST (4pm GMT/UK) to hear experts from Cmed Technology explain the pros and cons of eSource and EDC, and discuss if one is better than the other.

Hear from the following guest speakers from Cmed Technology:

  • Jon Carter, Product Manager
  • Catie Roland, Program Manager
  • Mark Tomlinson, Senior Director Technology Operations

This webinar will appeal to consultants and senior-level executives including directors, department heads and vice presidents involved in:

  • Clinical Research
  • Clinical Operations
  • Data Management

Listeners should leave the webinar with a solid understanding of the challenges that they would face if they were to adopt eSource for their next clinical trial and also an idea of how eSource will be used in the future.

For more information or to register for this event, visit EDC vs eSource: Is it Time to Move?

ABOUT CMED TECHNOLOGY:¬¬¬

Cmed Technology is the technology division of Cmed Group, with headquarters in Horsham, UK plus offices in Morrisville NC, Cambridge MA, San Bruno CA, Timisoara, Romania and Dublin, Ireland.

Cmed Technology is the developer of encapsia, an innovative, powerful, next-generation clinical data suite. Encapsia delivers a complete solution to gather and manage data in clinical trials with live insights and analytics on trial progress to inform and support management decisions. http://www.encapsia.com

Contact:
Dr Timothy Corbett-Clark, Chief Technology Officer
Cmed Group
Tel: +44 1403 755 050
Email: tcorbettclark@cmedtechnology.com

ABOUT XTALKS

Xtalks, powered by Honeycomb Worldwide Inc., is a leading provider of educational webinars to the global life science, food and medical device community. Every year thousands of industry practitioners (from life science, food and medical device companies, private & academic research institutions, healthcare centers, etc.) turn to Xtalks for access to quality content. Xtalks helps Life Science professionals stay current with industry developments, trends and regulations. Xtalks webinars also provide perspectives on key issues from top industry thought leaders and service providers.

To learn more about Xtalks visit http://xtalks.com
For information about hosting a webinar visit http://xtalks.com/why-host-a-webinar/

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Margot Rubin
Xtalks
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