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Webinar: Data Standards for eCOA in Clinical Trials
September 13, 2019 YPrime

September 13, 2019

Webinar: Data Standards for eCOA in Clinical Trials

MALVERN, P.A. – September 13, 2019 – Collecting data in a standardized way is the next step to reduce messy, time-wasting efforts that can negatively impact patient safety, development timelines and resource utilization. This is especially important given the rapid proliferation of eClinical technologies. In this free webinar, hear about Clinical Data Interchange Standards Consortium (CDISC) standards across data collection, tabulation, analysis and submission, with a particular focus on electronic Clinical Outcomes Assessments (eCOA).

Join YPrime’s Vice President of Clinical Analytics and Data Strategies, Terek Peterson, in a live webinar on Thursday, October 3, 2019 at 11am EDT (4pm BST/UK) to learn about the benefits of implementing standards and which forms of data collection standards companies are requesting.

The adoption of data standards for electronic Clinical Outcomes Assessments (eCOA), the fastest growing technology in the eClinical space, is critical to ensure quality and efficiency in this rapidly evolving discipline.

The presentation will include a discussion of the following:

  • Standardized eCOA deployment
  • Shifting industry attitudes and patient preferences
  • Growing scientific acceptability
  • Equivalence study conclusions
  • The importance of graphical control elements
  • Deployment considerations
  • Risk mitigation considerations

Terek Peterson has nearly 25 years of clinical research experience at biopharmaceutical companies and contract research organizations (CROs) leading clinical analytic and standards teams. He has contributed to the advancement of industry standards across study design, data collection, tabulation, analysis and regulatory submissions.

For more information or to register for this event, visit Data Standards for eCOA in Clinical Trials