The collection and analysis of standardised data from professional practices are particularly widespread within professional organisations, learned societies and networks. The organisation and content of these collections can take various forms: registry, observational studies, database. Integrated for the purpose of improving practices, these programmes constitute a CPD method. (Continuing Professional Development)
Telemedicine Technologies supports HCPs (Healthcare Professionals) and PSs (Professional Structures), with the technical implementation of these databases, as well as monitoring indicators and feedback to the actors of this registry (HCPs, PSs).
The registry incorporating the improvement process is set up and managed by a professional structure, made up of peers, this structure is responsible for:
• the theme (professional practices);
• the design of the approach;
• the quality of the data collected;
• the analysis and use of these practices.
The indicators put in place, targeted at key elements of practice and easy to collect, make it possible to objectify the quality of care and to monitor the improvement initiatives undertaken. Thus, in Data Visualisation, we can restore these indicators, by adding a comparative component. For example, each PDS can compare his practice with those of all the PDSs in his organisation or with the average practice of all the PDSs in his speciality, and more generally, with the whole practice of the PDS of a registry in a European registry.
Telemedicine Technologies also participates in the technical support of structures wishing to create European registries based on national registries existing in different countries, to create a common register with a minimum of information that is specific to each country and making it possible to centralise information from these different countries in a database, independent of each national registry and supplied from these national registries by interoperability with the desired update frequency.
Our Data Services structure can also offer the setup of European databases in CDISC format, to allow and facilitate exchanges with regulatory agencies.
A LEADING POSITION AND
AN INTERNATIONAL DEPLOYMENT
64 +
countries
involved
20 000 +
investigational
Centres
3 million +
patients
in database
50 000 +
users
worlwide
March 31, 2026
Applied Clinical Trials Online Clinical trials are growing more complex, and this trend will increase. Sponsors now expect seamless data capture from electronic systems, labs, wearables, patient-reported outcomes, and third-party sources, all feeding pivotal datasets. As data sources become more diverse and voluminous, the risk of integration and process errors rises. Small oversights in data […]
March 31, 2026
Medtech Dive FDA exempts more wearable, AI features from oversight In a pair of guidance documents, the regulator clarified the types of wellness features and clinical decision support tools that don’t fall under medical device oversight. By: Elise Reuter • Published Jan. 8, 2026 The Food and Drug Administration released two final guidance documents that would […]
February 26, 2026
During the EUCROF 2026 gala dinner in Amsterdam, in front of 300+ participants from the European clinical research ecosystem, the xShare project Open Call Awards for Clinical Research were officially presented. We are extremely proud that Telemedicine Technologies contributed to three complementary xShare Open Call projects (out of 10), all recognised for their quality, innovation […]