DATATRAK EDC/CDMS
Fountayn utilizes Datatrak’s EDC, the first EDC system established in 1991 with a proven and established track record of reliable and successful clinical trials that have obtained FDA approval. It is a FDA CFR 21 Part 11, HIPPA, GDPR, GCP compliant and validated software system. Datatrak’s EDC is well known for managing the most complex studies with robust and highly configurable customizations to meet any and all study needs. Its user interface is familiar to clinical and site professionals because no other EDC has a longer history of use in life sciences.
Fountayn is dedicated to empowering our clients with an EDC solution that makes collecting trial data as simple as possible. Our goal is for our clients to have efficient and successful studies by using a platform made specifically with them in mind.
Randomization and Trial Supply Management
We support all types of protocol requirements while dispensing, controlling, and automating drug and treatment supply fulfillment.
Easy Mid-Study Change Implementation
We take pride in our one-of-a-kind process that can allow teams to implement changes without any required study downtime or data migration.
Extensive Trial Design Capabilities
Work with our team of Trial Designers to create the study as needed to improve and enhance the end user experience.
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.
