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Revision of the In vitro diagnostic medical devices Directive Közzététel időpontja:: 22/03/2010, Utolsó frissítés: 25/04/2014

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Határidő: 15/09/2010

The European Commission has launched a public consultation on the technical aspects of the revision of Directive 98/79/EC on in vitro diagnostic (IVD) medical devices

Any comments and information on this public consultation should be submitted by mail, fax or email by 15 September 2010 at the latest to: European Commission Health and Consumers Directorate-General (DG SANCO) Unit SANCO B2, Cosmetics and Medical Devices B-1049 Brussels - Belgium, Fax: 00 32 (0) 2 296 64 67, email: SANCO-IVD-REVISION@ec.europa.eu