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Our Products


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.

Download: EasyClin®

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”.

EasyCRF (Clinical Record File)

Our eCRF includes a state-of-the-art tool for randomized trials, supportive functions to detect hidden events, as well as a deep learning mechanism to help you better analyze your medical data.

EasyISF (Investigator Study File)

The investigator-friendly solution to share documents with the sponsor.
Reduce the effort for monitoring visits and the burden for the study assistance. The commissioning can be ordered by the study sponsor at no cost to the study centre or as an internal clinic solution. Your study will always remain inspection ready and let auditors perform large parts of their regulatory inspections remotely.
We offer either on-premises installations, cloud-based installations and flat rate options depending on your needs and budget.


We offer support with the integration of technical systems into internal processes, as well as with the reorganisation. We help you to take the next step towards a digital company. Regulatory affairs, documentation, audits? That's our business. Every day.

You can also take it one step further - want to do a business health check of your company? Claim your free consultation! And we will tell you what it takes to become even more successful.

We Integrate With Your Ecosystem

Rely on us. Because you really can. 

After 30+ years in the industry, we know, what it takes to succeed in trials.

Give us a call or claim your free initial consultation! We would love to hear from you.

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