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About us

In the creation and implementation of medical studies and observational studies, we have had a close and lasting collaboration with CROs in various projects since 1999. We develop and operate various medical applications, such as EDC (Electronic Data Capture) web applications with electronic Case Report Forms as medical study platforms.

Your Feasibility Coordination Team welcomes you

In more than 20 years of cooperation, our team has become optimally attuned to each other. We have experts in study coordination, study conduct, medical documentation, data management, data analysis, medical IT and electronic study platforms. Together we have created the Feasyfy system and hope you will find it a clear and intuitive platform to use.

You can draw on our knowledge throughout the entire process of planning and study implementation.

We work with our quality management system according to ISO9001 and ISO27001. Our staff are trained and use SOPs to implement your projects. The IT processes and our Feasyfy application as part of the cvEDC system are validated and integrated into a computer system validation process. Our EDC system is fully based on the CDISC ODM standard

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Our system has been successfully validated several times in recent years by independent investigators as part of a drug trial, most recently in 2022. WSince 2023, we are ISO27001 certified.

Professional

Our employees are professional, resilient and motivated.

Please contact us at any time if you have any questions. You will find our contact details under your profile data after logging in.

Quality

We believe in the principle of quality and the high importance of good user experiences with our products.

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Please share your experiences with us and tell us which processes we can improve.

Reliability

The punctual and reliable delivery of the agreed products is an important factor in our customer relationship.

We guarantee quick feedback in case of queries or problems.

Legality

We comply with all legal frameworks. QM, ISO9001, CSV, GcP, GmP, GAMP, FDA CFR Part 11, ...