Are You Ready for Next Level Clinical Trials?
Digital Clinical Trials.
Time is Health.
Faster access to modern healthcare can save millions of people around the globe. This is why we emphasize so much on speeding up clinical trials. The faster new therapies and medical devices get on the market, the more lives can be saved.
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The successful acceleration on COVID-19 vaccination research is the best example.
Go Green. And ESG.
Time and money are resources, just as any other on the planet. Saving time and effort in your clinical trial makes your CO2 footprint smaller.
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Make your trial more sustainable, more helpful. And make life better - for all of us.
Discover our Fully Integrated Software Suite
for Global Biotech, Medtech, IVD and Pharma Trials.
Secure and Reliable, Complete End-to-End.
Audited and approved by:
ISO 14155
GAMP-5 / DTAC
FDA / EMA
Make Your Trials Faster.
More Cost-Effective.
More Sustainable.
And More Secure
(2-Way Encryption)*.
*coming soon
ISO 27001
ICH-GCP
21 CFR pt.11
We support and control your performance along the entire value chain of clinical trials. One main goal is to prevent all mistakes and an eventual trial failure due to process errors.
Our technology combines pre-trial services with clinical trial management and AI driven big data analytics in healthcare.
As a result, we massively raise efficiency and shorten development cycles, giving access to faster and cheaper healthcare to people around the world.
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Most importantly, you can rely on our professionalism and 100% commitment to quality.
Developed in the UK, Germany, and Austria.
GDPR / CCPA
ML, AI, Blockchain tools in development. Become a development partner!
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
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30+
Years of Experience
15
Business Partners
250+
Studies performed
78
Countries World Wide
5
Industry Awards
Our Partners
SynapCon GmbH
Frankfurt am Main
Germany
Commercial register: HRB 123878
VAT ID: DE346913109
Place of jurisdiction:
Frankfurt am Main
Managing Director: Sven Engel
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