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Catégorie : Calls and consultations

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EU reference laboratories (EURLs)

The European Commission may designate EU reference laboratories (EURLs) for high-risk in vitro diagnostic medical devices according to Article 100 of Regulation (EU) 2017/746. The EURLs have two main categories of tasks: advisory ones and...

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Have your say: Biotech Act

The consultation is addressed to citizens, innovators, entrepreneurs, industry, financial institutions, investors/venture capitalists, researchers/research organisations, civil society (including consumer, patient and environmental organisations), other users of biotechnologies, trade unions, national and regional authorities, and any...