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This screen gives access to a list of technologies and know-how of specific interest to researchers working on rare diseases. The list is sorted by country, region and city.
The technologies and know-how which are registered with Orphanet are those of specific interest for the rare diseases research, and taking place in Europe and surrounding countries. The information which is displayed is provided by the manager of the technological platform or expert methodologists.
The data is updated annually.
The data collection takes place in European and surrounding countries. Platforms funded by funding agencies outside of the Orphanet consortium are collected by the coordinating team if the funding agency is member of the IRDiRC consortium. The database cannot yet be regarded as comprehensive. If all technologies or know-how are not listed, it may be that we have not yet collected all the information, but it is also possible that the professional has refused to be listed.
Orphanet aims to provide rare disease information to healthcare professionals, patients, and their relatives, in order to contribute improving the diagnosis, care and treatment of these diseases. Information in Orphanet is not intended to replace professional health care.
Orphanet cannot be held responsible for harmful, truncated or erroneous use of any information found in the Orphanet database.