EU action in newborn screening for rare diseases
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The document discusses European Union actions related to newborn screening for rare diseases. It provides background on EU health policy and legislation regarding rare diseases. It then summarizes an evaluation launched in 2009 on newborn screening practices for rare diseases across EU member states. The evaluation includes reports on current practices, an expert opinion on developing EU policies, and establishing an expert network on newborn screening.
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EU action in newborn screening for rare diseases
- 1. European Union action in the field of newborn screening for some rare diseases Amsterdam, 14th May 2011 Antoni Montserrat Moliner Policy Officer for Rare Diseases DG SANCO Health Information Unit European Commission
- 16. DG SANCO priorities on rare diseases Web site Public health actions http:// ec.europa.eu/health/rare_diseases/policy/index_en.htm Contact point at DG SANCO [email_address] Research actions http://ec.europa.eu/research/health/medical-research/rare-diseases/index_en.html Contact point at DG RTD [email_address]