Global provider of eCOA solutions


Supporting sponsors, pharmaceutical companies, biotechnology companies and CROs, we aim to improve clinical trials with innovative and intuitive eCOA solutions, for better data quality and trial efficiency.

Global solutions for supervised
and unsupervised eCOA


We offer a wide range of solutions to fit each study and therapeutic area. Our devices are designed to improve clinical trial compliance and reduce data capture errors with intuitive, efficient and user-friendly solutions for patients. With safe and real-time data capture, patients and sponsors fully benefit from the advantages of electronic solutions, adapted to both supervised and unsupervised clinical studies.

Committed to improve
the quality of clinical studies


Over 10 years of global eCOA experience has allowed us to build powerful tools and services that help sponsors to collect complete, accurate and reliable data. Two of our main areas of expertise are related to:

• Improving patient engagement
Patient engagement is key to increasing both the quantity and quality of clinical trials data while ensuring compliance regarding taking the clinical trial drug(s), filling diaries, and remaining actively involved in the trial.
This increase in quality generates overall savings in the budget for the trial while at the same time increasing relevant data collection.

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• Allowing risk-based monitoring
We provide automated and ad hoc Key Performance Indicators (KPIs) that enable risk-based monitoring. These include signals based on our global experience of work with clinical trial sites, with information coming from our Webportal, our project managers (PMs), our data management (DM) activity and our support team. These KPIs give our customers and partner CROs a clear view of what may go right or wrong on-site, and allow appropriate corrective actions to be put in place immediately if necessary.
This approach generates better overall data quality and allows for targeted and very efficient monitoring.

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Latest news

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    KAYENTIS announces its participation in the Avoca Diligent Prequalification Platform, the dedicated platform to efficiently select your clinical trial provider

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Agenda

  • 07 November
    DMB "Clinical Data, real Data, Open & Big Data" - Cité Internationale, Paris, France
  • 16 November
    Partnership in Clinical Trials - Vienne, Austria
  • 16 May
    OCT Europe 2017 - Outsourcing in Clinical Trials - Barcelona, Spain
  • Linkedin updates