Our goal is to provide you with 100% reliable, yet profitable advantages from the current challenges of the market. Leave your worries and concerns with us. Start fast, early and safe!
We have market knowledge of the entire medical value chain
and fully hand over this advantage to you - our clients.
The commitment and technical expertise we share helps
shorten your development cycles. We ensure faster patient care and reduce development costs to make innovative medical work
more affordable and accessible to everyone.
Welcome to the EasyClin® Software Suite.
Let's see what it contains.
EasyTMF (electronic Trial Master File)
Our future-proof clinical trial document management is based on 20 years of experience. It is intuitive, easy-to-use, fully regulatory compliant and meeting the daily demands of a clinical trial. Our setup services include training, SOP support and regulatory consulting. Adaptations are possible and already have been pre-validated. Your study will be inspection-ready at any time and auditors can access all documents and date from remote. The system ensures full regulatory compliance with EU-GDPR, US 21CFR Part 11 and ICH-GCP E6 R2.
EasyFEA (Feasibility Tool)
Do you need suitable study sites for a clinical project? Do you want to make your study centre selection GDPR compliant and minimise legal risks?
That’s where our EasyFeasibility takes action. We not only connect the suitable partners, but we also automate the qualitative assessment and add an analysis of potential risks on top. This leads to a cost reduction up to 90% for the “study site selection”.