SynapCon’s revolutionary approach to efficient software solutions for clinical trial management to enable faster drug development is capturing the attention of investors worldwide.
Speak to us today about the opportunities available.
Site Feasibility and Clinical Trial Management
Our feasibility platform radically simplifies feasibility studies, by simplifying the process of site selection for sponsors, contract research organization, investigators, and study sites.
Our Clinical Trial Management software systems (CTMS) design, based on more than 20 years´ of experience in client trials, provides our clients with the peace of mind that their clinical trial will be fulfilled quickly and efficiently, conform with EU-GDPR (General Data Protection Regulation) and ICH GCP (Good Clinical Practice).
Our newest developments will implement AI-assistance for site feasibility and clinical trial management.
Expert management
Our senior management team has more than 30 years’ experience in software development as well as practical experience in clinical trial management and drug development.
Explosive Demand
Software solutions in clinical trial management and drug development are one of the world’s fastest-growing industries, with demand set to grow at a CAGR of 13% until 2025.
Global Expansion
Our client network spans from North America, Europe, to Japan and we are actively expanding to more locations around the world.
Who we are looking for
Ideally, you are already invested in the medical field and have the expertise to make an appropriate investment decision. Your organization possesses a broad network in life sciences, ideally in clinical trials and pharma.
You have sufficient capital to support a project of this size over several funding rounds. You actively support us in the search for further investors to accelerate the global expansion of our business.
We kindly ask business angels to refrain from contacting us.