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Kayentis and ClinOne combined solution

eConsentInteroperability
Last updated: June 24, 2024

Improve your eCOA data collection and clinical trial efficiency thanks to Kayentis and ClinOne combined solution!


Ease the patient and site journey with a unique access to:

  • eCOA data collection
  • Consent Management
  • Virtual Visits
  • Patient Engagement features
  • Site efficiency features
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About the author
Picture of Marc Chaperon

Marc Chaperon

Estelle brings 20+ years of experience in pre-clinical and clinical research from Top 5 Pharma and Biotech firms. Leading projects across Phases 1 to 4 in diverse therapeutic areas, she offers deep insights into clinical science, operations, and regulatory intricacies. Appointed as Chief Medical Officer at Kayentis in May 2019.
Meet us at the following events

SCOPE Europe 2025

OCT 14-15 2025 • Barcelona, Spain
SCOPE Europe | Summit for Clinical Operations Executives | October 14-15, 2025 |Barcelona, Spain

Rethinking Phase 1 Oncology Trials with Electronic Patient-Reported Outcomes

November 4 • 11-12AM EDT / 4-5PM GMT / 5-6PM CET
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The primary aim of Phase 1 oncology clinical trials is to determine the safety of a new treatment, and to...