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

  • 2019 employee satisfaction survey
    2019 Employee Satisfaction Survey

    Embrace our spirit! With a 19% increase in… | Read More

  • Ophthalmology
    eCOA in ophthalmology

    There is an extended use of Patient Reported… | Read More

  • Key #5 for successful ePRO selection in your ophthalmology clinical trial: Anticipate cultural differences in multi country clinical trials

    Before selecting a PRO for use in a… | Read More

  • patient nurse tablet
    Key #4 for successful ePRO selection in your ophthalmology clinical trial: Consider the method of ePRO administration

    PROs in ophthalmology trials can either be self-administered… | Read More

  • Key #3 for successful ePRO selection in your ophthalmology clinical trial: Get your patients involved

    Although clinical research stakeholders strive to be patient-centered… | Read More

Agenda

  • 26 October
    OCT Europe 2020 - October 26-27 - Paris, France - Booth #83 - Schedule a meeting with Kayentis
  • 02 November
    Clinical Trials Europe - Nov 2-4 - Amsterdam, The Netherlands - Booth #88 - Schedule a meeting with Kayentis     Clinical Trials Europe
  • 08 November
    DIA Japan - Nov 8-10 - Tokyo Big Sight, Ariake - Booth #17 -  Schedule a meeting with Kayentis