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A registry is defined by the French Registry Evaluation Committee (CER), as a structure carrying out continuous and exhaustive collection of personal data related to one or several health events, within a geographically-defined population, for research purposes and public health surveillance, conducted by skilled team.

Our objectives are:

Health monitoring and surveillance

Aetiological research

The registry has a central role in research on childhood cancer risk factors through its exhaustive database and precise diagnosis information, which is coded to international standards.

These studies are conducted within INSERM-1153 unit, Team 7 (EPICEA).

Contribution to health services evaluation