Improving and accelerating electronic data capture (EDC) setup times in clinical trials can deliver tangible results and valuable efficiencies.  

Reducing the collection and management time of data capture is key to avoiding workflow bottlenecks. As technological advances continue to enhance clinical trial processes, drastically reducing data capture setup times is becoming ever more important.

Strategies for delivering optimal EDC timelines are a major industry focus. In a forthcoming webinar, experts from CRScube and VITA Global Sciences will explore EDC workflow issues and solutions – and the system setup will be demonstrated and commented on in real-time.

The growing importance of faster clinical trial data capture

As clinical trials become more expensive and complex, it has become increasingly important to streamline as many processes as possible. Less time must be spent on manual inputs, and more efficient workflows are required to deliver stronger results.

The importance of clinical trial and data capture has increased in line with tightening budgets, furthering the need for optimised clinical trial processes.

A unified platform can eliminate both duplicate data entry and laborious cross-system reconciliation, making the clinical data management system (CDMS) a single source of truth for all trial data.

With new technology enhancing electronic data capture (EDC), randomisation and trial supply management (RTSM), and electronic patient reported outcomes (ePRO), sponsors and CROs can gain significantly from a one-stop solution that reduces integration bottlenecks to provide end-to-end visibility across the trial lifecycle. These aspects and more will be discussed in an upcoming webinar by CRScube.

Verifying the value of optimised electronic data capture (EDC)

Depending on the overall complexity of a clinical trial process, the study build timelines can be lengthy. With some CROs using separate platforms to manage specific clinical data, it can further complicate the setup and run times of a trial.

Through a unified platform, the CRScube solution increases the speed of EDC system setup and accuracy of clinical data capture. With its focus on integrated platform functionality, CRScube also nurtures greater patient engagement, delivering a collaborative approach for all involved in electronic clinical data acquisition.

Advantages include reduced costs, improved data quality, delivering more real-time access to clinical data and monitoring, as well as ensuring a greater level of stakeholder communication. Crucially, outcomes for clinical trials are improved.  

As CRScube continues to focus on EDC platforms, its forthcoming webinar will deliver insights from experts at the company and Vita Global Sciences about the advantages of optimal data management solutions in clinical trials. The webinar will also feature a study build in real-time using the CRScube platform.

The speakers for the webinar are:

  • Sylvain Berthelot, VP strategy and marketing at CRScube
  • Dennis Yoo, sales and marketing associate at CRScube
  • Kelly Forester, senior director of DM solutions and services at VITA Global Sciences

To learn more about this event and for further information on the speakers involved, click here.