As experts in electronic data capture for patients in clinical trials, Kayentis has been involved in clinical development since 2003, helping sponsors and CROs to bring simplicity to the collection of clinical trials data for both patients and sites. Kayentis offers a wide range of eCOA solutions that are compatible and can be adapted for all clinical trial needs. Offering new perspectives to improve the quality of clinical trials, we provide solutions to maximize patient engagement and compliance.
Through the quality of the solutions, services, and databases that we provide to sponsors and CROs, we contribute to the reliability of clinical research and help to improve human health.
16 years of eCOA experience in a broad range of therapeutic areas
eCOA is not a one-size-fits-all solution; the complexity lies in the large number of therapeutic areas and the associated needs, requirements, challenges, and regulations.
Thanks to our experience and the high level of flexibility of our eCOA solution, we can adapt according to your specific therapeutic area, clinical development stage, and patient population
We can also provide the possibility to connect to medical devices specific to your therapeutic area – oncology, rare disease, immunology, ophtalmology… -, or to your population – pediatric… -, to optimize your data collectionDISCOVER OUR CASE STUDIES BY THERAPEUTIC AREAS
Our global capabilities and local operational teams
We have 3 operational sites globally (US, Europe, and Asia) with project management and data management capabilities, allowing us to be as close as possible to your operational teams.
We are committed to support key stakeholders in clinical trials and collaborate with diverse associations to continuously improve our solutions and our range of services.
We are involved in the ePRO consortium to help to advance the future of clinical trials and contribute to ongoing scientific research
We also regularly collaborate with sites and patient associations.