DISCOVER
REGISTRIES
REGISTRY OF PRACTICES, OBSERVATIONAL STUDIES, DATABASE
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)
HEALTH
PROFESSIONALS
AND PROFESSIONAL STRUCTURES
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.
EUROPEAN
REGISTRIES
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
LATEST NEWSOUR NEWS >
April 29, 2025
May 5 & 6 – Basel Telemedicine Technologies is pleased to present its CleanWeb™ eClinical suite, offering flexible, regulatory-compliant solutions tailored to every phase of clinical trials. Our platform includes a wide range of modules, such as eCRF, Randomization & Trial Supply Management, ePRO, eTMF, eConsent, Data Visualization, Vigilance, Imaging, CTMS, and more. We invite […]
April 29, 2025
Fierce Biotech The average cost for a Big Pharma to develop a drug in 2024 was $2.23 billion, up from $2.12 billion the year before. The data come from 20 pharmas that had the highest R&D budgets in 2020, as reported in Deloitte’s annual report, “Measuring the return from pharmaceutical innovation.” In 2024, the average […]
April 29, 2025
Biopharm International In January 2025, Samsung Biologics signed a six-year, $1.4 billion contract manufacturing agreement with an as-yet undisclosed European pharmaceutical company, with production to take place at Samsung’s manufacturing site in Songdo, South Korea (1). Simultaneously, at the J.P. Morgan Healthcare Conference held in San Francisco, the company announced plans to complete construction of […]