The European Medicines Agency is a decentralised body of the European Union. Its main responsibility is the protection and promotion of public and animal health, through the evaluation and supervision of medicines for human and veterinary use. Terminology work for this agency in 2009 focused on EMA’s glossary of key terms which now contains more than 250 terms in all official EU languages. The National Competent Authorities (NCAs) were invited to finalise their work on validation of pending terms in this glossary so that all entries could be processed by the Centre and subsequently be imported into IATE to make them accessible to users worldwide.
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Wednesday, 24 August, 2016