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
3 million +
patients
in database
50 000 +
users
worlwide
MEMBER OF
LATEST NEWSOUR NEWS >
September 2, 2024
17 September 2024 – 11am – 12:30pm EDT Register for this webinar to receive essential updates on the CDISC transition and learn about new regulations and initiatives impacting Trial Master Files (TMF). Don’t miss this opportunity to stay informed about the latest industry standards and practices. Read more and register: https://cdisc.zoom.us/webinar/register/WN_WqNz9_hiRVihH_pe1IEurA#/registration
September 2, 2024
Med City News Innovation is not just a luxury but a necessity in the realm of clinical trials, particularly as we strive to accelerate drug development. Yet, the slow pace of innovation within the U.S. clinical trials system has impeded progress, leaving many stakeholders frustrated. U.S. Food and Drug Administration (FDA) resource limitations cause the […]
September 2, 2024
International Biopharma Data integrity is critical in Biopharma manufacturing yet is often difficult to achieve due to complex regulatory requirements and legacy data management systems, among the many factors. Furthermore, issues such as data accuracy, completeness and security impact product quality, regulatory compliance and ultimately patient safety. Addressing all these challenges demands a multifaceted approach […]