Digital Clinical Trials. Global Compliance. Real Results.
From feasibility to submission — SynapCon© unites sponsors, CROs, and investigators in one validated, cloud-ready ecosystem.
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Explore EasyClin©Suite
Experience EasyClin® – Live Sandboxes
Sandbox 1: Site Selection
EasyFeasibility© – Smarter Investigator & Site Selection
Evaluate, invite, and qualify study sites worldwide.
Our digital feasibility module automates outreach, collects investigator data, and generates validated feasibility reports — all in line with ICH-GCP and 21 CFR Part 11.
Sandbox 2: EasyTMF® / EasyISF©
Digital Document Management – Sponsor & Site Views
Discover how centralized and site-specific trial documentation work together.
EasyTMF© and EasyISF© provide real-time access, full audit trails, and seamless document exchange between sponsors and investigators.
Why SynapCon:
The Control Center for Digital Clinical Trials.
Manage feasibility, documentation, and compliance across studies — all within the EasyClin® suite.
We simplify complexity. SynapCon© provides an end-to-end digital suite for Biotech, MedTech, and Pharma — combining speed, compliance, and innovation.
Faster decisions, fewer risks, full transparency.
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⏱ Accelerate Trials – Reduce site selection and setup time by up to 60 %.
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🧠 Stay Compliant – Built to ISO 13485, ISO 27001, ICH-GCP, 21 CFR Part 11, and HIPAA.
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💰 Save Costs – Lower operational expenses by > 40 % through automation.
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Explore EasyClin©Suite
30+
Years of Experience
6
Partners
250+
Studies
performed
78
Countries
12
Awards
From Paper Work to Patient Work.
Customer benefit
We massively reduce the trial time needed from pre-clinical and in-house setup through
clinical trials and final evaluation.
Customer experience
Our service does not end after we sold our product. That's where it starts. We support you in all questions of FDA, GDP or other audit related topics.
Customer
journey
After 30+ years of experience, we guarantee audit-proof systems and work. And we provide additional support at any time of your trial, if needed.
From Patient Work to Peoples Health.
Patient
benefit
Patients can be approached more quickly and effectively to participate in trials. In many indications, these trials can be life-saving.
Patient
experience
Faster and more targeted enrolment into clinical trials can provide optimal treatment strategies and give many people the hope of a happy and healthy life.
Patient
journey
Patients often go through a long ordeal before they are diagnosed. This needs to change in order to strengthen the patient and enable them to return to their previous life.
From Peoples Health to Social Responsibility
Social
benefit
With faster access to the latest treatments, many people are able to participate in life and work again. This is a huge relief for the community.
Environment
benefit
Our technologies reduce energy consumption and the cost of clinical trials. This benefits society.
Fast.
Reliable.
Affordable.
Compliant.
SynapCon offers the first fully integrated all-in-one digital solution for the drug development and clinical trials market, addressing a very specific and complex clinical and medical workflow with high recurring revenues and market share potential.
Easy to use and affordable for all, it disrupts the old-fashioned, paper-based trials industry in an attractive and modern way.
Publicly sponsored by 2 German ministries:
Federal Ministry of Economic Affairs & Energy
Federal Ministry of Education and Research