Evaluating an eClinical Provider to Meet the Needs of Modern Trials

Using Electronic Data Capture EDC and other eClinical tools such as electronic patient-reported outcome (ePRO), eConsent, and Direct Data Capture  (DDC) has become the norm for the collection of clinical and patient-reported data in clinical research, however, there are 100s of varied eClinical platforms available to sponsors and Contract Research Organizations (CROs) and it can be difficult to ensure that you select the best fit for your study design during your evaluation process. Furthermore, as regulatory guidelines push for new methods of data collection and new clinical trial models emerge (hybrid/virtual trials), how do you select an eClinical provider capable of supporting you through the clinical trials of tomorrow?

Looking to the future, it is clear that Sponsors and CROs need eClinical platforms that allow for flexible clinical and patient-reported data collection, real-time data access and insights and give them the peace of mind they need to make strides in a changing environment. 

During this free live webinar we will discuss:

• The current eClinical landscape, and how to classify vendors during your evaluation
• Clinical research trends and their associated technology and data collection needs
  • Hybrid/Decentralized Trials
  • Regulatory Guidelines
  • Patient-centricity
• How a Unified eClinical Platform offers benefits over a Traditional eClinical Platform, and how to select an eClinical provider that offers modern technology with a proven platform you can trust