We are here at Booth #32 in Prague at the International Conference on Pharmacoepidemiology. Stop by for a demo and conduct your own search!

View our latest newsletter announcing B.R.I.D.G.E. TO DATA® capabilities at the 34th International Conference on Pharmacoepidemiology & Therapeutic Risk Management.

If you will be attending, stop by booth #32 for a demo and conduct your own search!

The Spanish Rare Diseases Patient Registry [Registro Nacional de Enfermedades Raras] is a registry of national scope which collects information on all persons diagnosed with any disease considered to be rare or of low prevalence. The objectives of the registry are to:
- Provide necessary information to contribute to the development of new treatments and to the prevention, diagnosis, prognosis and quality of life of rare disease patients and their families;