The catalog contains the description of the main databases in public health in France
October 23 2017
The objective of the programme is to improve quality in the collection of samples and data, the design of new modules and tools, and improve interoperability to improve epidemiological, clinical, fundamental and translational research and medical practices in these pathologies.
Three areas of work have been defined:
- WP1: data collection and data management
- WP2: development of the clinico-biological sarcoma database
- WP3: communication.
October 20 2017
To evaluate the incidence of seizures in Réunion's population.
To determine the risk factors specific to Réunion among epileptic patients
October 20 2017
To study the conditions under which surveys of this type are conducted and extended on a larger scale, and to prepare recommendations for the purpose of achieving a better inclusion of homeless people in the general census of the population, as well as in surveys that are regularly carried out only among those with housing. A first examination of the processes leading to homelessness was also expected.
October 20 2017
To calculate the prevalence of psychiatric disorders in the prison environment
The catalog contains the description of the main databases in public health in France
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