|
|
|
|
Several challenges can hinder the adoption of Electronic Clinical Outcome Assessments (eCOA), discouraging some organizations to the point of reverting to paper-based COAs for non-pivotal studies. To unlock the full potential and benefits of eCOA, a paradigm shift is necessary. Explore six pivotal areas where eCOA standards can be improved.
|
|
|
|
|
The clinical trial landscape is evolving rapidly, but is eCOA/ePRO keeping pace? Learn how to modernize ePRO delivery to better serve modern trials. Watch this on-demand conversation to learn how to streamline ePRO design and launch, ensuring rapid build times, efficient operations, and high-quality data.
|
|
|
|
|
How can you combat the instrument licensing and linguistic validation challenges associated with adopting eCOA and overcome first-patient-in (FPI) milestone delays? Early engagement in the licensing process, coupled with careful selection of CROs, could present a solution, facilitating fast access to necessary source files.
|
|
|
|
|
User Acceptance Testing (UAT) plays a pivotal role in ensuring the success and reliability of electronic Clinical Outcome Assessment (eCOA) data, yet it is often overlooked until the final stages of delivery. Proactive planning and early UAT involvement in the eCOA design process can substantially improve quality, efficiency, and consistency.
|
|
|
|
|
|
Veeva eCOA Demo
|
Veeva eCOA makes study management faster and easier for everyone involved. Learn how the modern build platform, including a ‘one-click’ library of pre-validated questionnaires, reduces build times by 75% and means mid-study updates can be actioned in minutes.
|
|
• Request Information
|
|
|
|
|
|
|
|
