Telemedicine Technologies
develops e-Health solutions
to reinvent the organisation of healthcare in 5 key domains
Clinical Research
A flexible and modular offer that fully meets your needs…
Managed Access Programmes
Ethical and compliant mechanism for access to drugs…
Real-World Evidence & Registries
Support for healthcare professionals in the technical implementation of registry databases and set-up of monitoring indicators …
Patient Pathway
Plan, rationalise and standardise the care of your patients through medical protocols…
Investigator site Management
For an efficient Site Management in Clinical Research...
DISCOVER
eCRF • ePRO/eCOA • eConsent • IWRS • IMP Management Vigilance •
Imaging • eTMF • CTMS • rSDV • MAP
Do you want to learn more about our e-health solution? Just fill in the form and we will get back to you shortly
OUR SERVICES
Data Services
WE CARE FOR YOU DATA
Quality of Data through comprehensive clinical Data Management...
AI & Data Visualisation
ARTIFICIAL INTELLIGENCE EMPOWERING OUR SOLUTIONS AND DATA SERVICES
Advanced data processing based on machine learning and advanced statistics
Training
SKILLS TRANSFER & END-USER AUTONOMY
Our training courses have been awarded the national Qualiopi certification…
User Support
AVAILABLE IN FRENCH AND ENGLISH
User support is available in both French and English...
Hosting
SECURE OR HEALTH DATA HOSTING SERVICES
Secure hosting or Health Data Hosting services, at your convenience...
A LEADING POSITION AND
AN INTERNATIONAL DEPLOYMENT
64 +
countries
involved
20 000 +
investigational
Centres
2 million +
patients
in database
50 000 +
users
worlwide
MEMBER OF
LATEST NEWSOUR NEWS >
September 29, 2023
17-18 Oct 2023 Building on the success of its long-running US-based counterpart, the 6th Annual SCOPE Europe: Summit for Clinical Ops Executives is a two-day executive conference serving clinical innovation leaders, clin ops execs, digital leaders, functional heads, category managers, and those responsible for the planning and management of clinical trials in Europe and the […]
September 29, 2023
Biopharm International On Sept. 21, 2023, FDA released a new guidance on how the agency plans to utilize alternative tools to remotely evaluate drug manufacturing facilities identified in a marketing application. The application may be a new drug application, an abbreviated new drug application, a biologics license application, or a supplement to any of these […]
September 29, 2023
Applied Clinical Trials While many US-based biopharma start-ups are interested in conducting clinical trials in Europe, they are often unfamiliar with European legislation and regulations. Some of the biggest misconceptions are around start-up timelines. Typically, the time it takes to go from initial clinical trial application to delivering the first dose to a patient takes […]