Viešosios konsultacijos
Revision of the In vitro diagnostic medical devices Directive
- Galutinis terminas:
- Galutinis terminas: 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
Dokumentai ir nuorodos
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Privacy statement
(16 KB)
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Questionnaire
(49 KB)
Susisiekite
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