Direct-To-Patient Data Management Throughout Your Entire Development Lifecycle
With a patient-centric, remote and holistic approach, our team helps you accelerate data recovery. From pre-approval virtual clinical trials to real-world post-marketing surveillance studies, together, let’s create new designs and perspectives for your local or global projects.
Whether you need to understand which asset best aligns with your long-term strategy, which new market or therapeutic area to explore, or how to expand into another sector, we are ready to help you lead the way.
Pre-Approval Virtual Trials
Efficiently and securely collect clinical data from patients and devices, thanks to our integrated eCRF, ePRO and eCOA solutions.
RWE and Post-Market Surveillance Studies
Capture secure real-time data from devices and patients with our ePRO and eCOA solutions and ensure compliance with EU MDR, IVDR and CE mark.
Value-Added Services
Integrate your own connected devices directly within our seamless platform and create a white label application directly to market
Technology integration for IoT MD
With over 120 transactions closed over the last 10 years, our strong track record and adaptive methodology allow you to get the most out of your divestments
