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Corrigendum to Regulation (EU) No 528/2012 of the European Parliament and of the Council of 22 May 2012 concerning the making available on the market and use of biocidal products (OJ L 167, 27.6.2012)

CELEX number:
32012R0528R(08)
Form:
Corrigendum, Regulation
Author:
European Parliament, Council of the European Union
Date of document:
28/10/2017; Date of publication
Number of pages:
1

Amended proposal for a REGULATION OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL amending Regulation (EC) No 726/2004 as regards information to the general public on medicinal products for human use subject to medical prescription

/* COM/2012/049 final/2 - 2008/0255 (COD) */

CELEX number:
52012PC0049R(01)
Form:
Corrigendum, Proposal for a regulation
Author:
European Commission
Date of document:
10/02/2012

Proposition modifiée de DIRECTIVE DU PARLEMENT EUROPÉEN ET DU CONSEIL modifiant la directive 2001/83/CE en ce qui concerne l’information du public sur les médicaments soumis à prescription médicale, d’une part, et la pharmacovigilance, d’autre part

The corrigendum does not concern the English version.

/* COM/2011/0633 final/2 - 2008/0256 (COD) */

CELEX number:
52011PC0633R(01)
Form:
Proposal for a directive, Corrigendum
Author:
European Commission
Date of document:
11/10/2011

Proposal for a Regulation of the European Parliament and of the Council laying down procedures relating to the application of certain national technical rules to products lawfully marketed in another Member State and repealing Decision 3052/95/EC {SEC(2007) 112} {SEC(2007) 113}

/* COM/2007/0036 final/2 - COD 2007/0028 */

CELEX number:
52007PC0036R(01)
Form:
Corrigendum, Proposal for a directive
Author:
European Commission
Date of document:
14/02/2007
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Domain: EU law and case-law, EUROVOC descriptor: market approval, Type of legislative procedure: Co-decision procedure (COD), Form: Corrigendum, Search language: English