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Built to meet 21 CFR Part 11, GCP, and HIPAA standards.
Configure forms, workflows, and reports to fit your unique study requirements.
Reduce fragmentation with seamless CDMS, CTMS, and ePRO integration.
Traditional EDC systems can be rigid, complex, and costly. Fountayn’s Electronic Data Capture (EDC) software is designed to streamline clinical data collection, enhance flexibility, and ensure compliance—without the usual headaches
Get your trials up and running in weeks, not months.
Reduce training time and improve user adoption.
Make data-driven decisions with instant access to study data.
Adjust to your study needs without costly reconfigurations.
“Fountayn is the best product suite assisting in any clinical trials – from simple to complex studies, even those in the oncology therapeutic area. It brings in cost efficiency and all features are built in a single platform.“
Tsubasa Iwata, Representative Director
Tsubasa Iwata,
Representative Director
Our goal is for our clients to have efficient and successful studies by using an EDC platform made specifically with them in mind.
Work with our team of Trial Designers to create the study as needed to improve and enhance the end user experience.
We take pride in our one-of-a-kind process that allows teams to implement changes without any required study downtime or data migration.
Whether you’re managing a small-scale study or a global clinical trial, our EDC for clinical trials adapts to your workflow – giving you full control over your data without the need for complex custom coding.
Take control of your clinical trials with a smarter, faster, and more intuitive EDC system.
“The team was great to work with and they made sure the eCRFs looked and worked well. It makes them an easy choice for EDC referrals.”
“Utilizing Randomization within their EDC makes it easier for the sites, providing a seamless process."
Traditional EDC systems can be rigid, complex, and costly. Fountayn’s Electronic Data Capture (EDC) solution is designed to streamline clinical data collection, enhance flexibility, and ensure compliance—without the usual headaches
We support all types of protocol requirements while dispensing, controlling, and automating drug and treatment supply fulfillment.
Powerful reporting gives study teams the ability to easily access, filter, and export real-time study data into clear and concise reports whenever they are needed.
Get your trials up and running in weeks, not months.
Get your trials up and running in weeks, not months.
Make data-driven decisions with instant access to study data.
Adjust to your study needs without costly reconfigurations.
Take control of your clinical trials with a smarter, faster, and more intuitive EDC solution.
“The team was great to work with and they made sure the eCRFs looked and worked well. It makes them an easy choice for EDC referrals.”
“Utilizing Randomization within their EDC makes it easier for the sites, providing a seamless process."
“The system is easy to use, you can create customized forms, manage study participants, securely store and manage data.”