Global provider of eCOA solutions


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

Global solutions for supervised
and unsupervised eCOA


We offer a wide range of eCOA 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 eCOA 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.

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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Latest news

  • Associations
    Kayentis gives back to its community by donating to two local associations

    Aware of its responsibility towards the environment, Kayentis… | Read More

  • Kayentis extends its contribution to scientific research in clinical trial endpoint assessment and joins the Critical Path Institute’s ePRO Consortium

    Kayentis announces that it has joined the C-Path’s… | Read More

  • eCOA study: Paper back-up and data reliability

    eCOA study: the impact of a paper back-up… | Read More

  • press-release
    Press Release // Kayentis appoints Estelle Haenel as medical director

    25-year pharma industry veteran and clinical trials expert… | Read More

  • Inclusion and gender diversity is not a given!

    This can only be the result of a… | Read More

Agenda

  • 22 October
    OCT Nordics - Oct 22&23 - Copenhagen, Denmark - Booth #10 - Schedule a meeting with Kayentis
  • 02 November
    ISPOR - Nov 2-6 - Copenhagen, Denmark - Schedule a meeting with Kayentis   ISPOR
  • 10 November
    DIA Japan 2019 - Nov 10-12 - Tokyo Big Sight, Ariake - Booth #42 -  Schedule a meeting with Kayentis
  • 19 November
    DMB - Nov 19 - Paris, France - Booth #14 - Schedule a meeting with Kayentis
  • 19 November
    Clinical Trials Europe - Nov 19-21 - Barcelona, Spain - Booth #51 - Schedule a meeting with Kayentis   Clinical Trials Europe
  • Linkedin updates