Accept Refuse

EUR-Lex Search results

Back to EUR-Lex homepage

This document is an excerpt from the EUR-Lex website

Search Results

Search for: 90/385/EEC, Search language: English
2

Regulation (EC) No 1907/2006 of the European Parliament and of the Council of 18 December 2006 concerning the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH), establishing a European Chemicals Agency, amending Directive 1999/45/EC and repealing Council Regulation (EEC) No 793/93 and Commission Regulation (EC) No 1488/94 as well as Council Directive 76/769/EEC and Commission Directives 91/155/EEC, 93/67/EEC, 93/105/EC and 2000/21/EC

OJ L 396, 30.12.2006, p. 1–850 (ET, LV, LT, MT, SK)
OJ L 396, 30.12.2006, p. 1–849 (EN, FR, IT, SL, FI, SV)
OJ L 396, 30.12.2006, p. 1–851 (CS, DE, HU)
OJ L 396, 30.12.2006, p. 1–848 (NL)
OJ L 396, 30.12.2006, p. 1–853 (EL)
OJ L 396, 30.12.2006, p. 1–852 (ES, DA)
OJ L 396, 30.12.2006, p. 1–794 (PL)
OJ L 396, 30.12.2006, p. 1–854 (PT)
This document has been published in a special edition(s) (BG, RO, HR)

In force

CELEX number:
32006R1907
Author:
European Parliament, Council of the European Union
Date of document:
18/12/2006

Regulation (EU) 2019/1020 of the European Parliament and of the Council of 20 June 2019 on market surveillance and compliance of products and amending Directive 2004/42/EC and Regulations (EC) No 765/2008 and (EU) No 305/2011 (Text with EEA relevance.)

PE/45/2019/REV/1

OJ L 169, 25.6.2019, p. 1–44 (BG, ES, CS, DA, DE, ET, EL, EN, FR, GA, HR, IT, LV, LT, HU, MT, NL, PL, PT, RO, SK, SL, FI, SV)

In force

CELEX number:
32019R1020
Author:
European Parliament, Council of the European Union
Date of document:
20/06/2019; Date of signature

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 Text with EEA relevance

OJ L 167, 27.6.2012, p. 1–123 (BG, ES, CS, DA, DE, ET, EL, EN, FR, GA, IT, LV, LT, HU, MT, NL, PL, PT, RO, SK, SL, FI, SV)
This document has been published in a special edition(s) (HR)

In force

CELEX number:
32012R0528
Author:
European Parliament, Council of the European Union
Date of document:
22/05/2012

Regulation (EU) 2017/746 of the European Parliament and of the Council of 5 April 2017 on in vitro diagnostic medical devices and repealing Directive 98/79/EC and Commission Decision 2010/227/EU (Text with EEA relevance. )

OJ L 117, 5.5.2017, p. 176–332 (BG, ES, CS, DA, DE, ET, EL, EN, FR, GA, HR, IT, LV, LT, HU, MT, NL, PL, PT, RO, SK, SL, FI, SV)

In force

CELEX number:
32017R0746
Author:
European Parliament, Council of the European Union
Date of document:
05/04/2017; Date of signature

Directive (EU) 2019/904 of the European Parliament and of the Council of 5 June 2019 on the reduction of the impact of certain plastic products on the environment (Text with EEA relevance)

PE/11/2019/REV/1

OJ L 155, 12.6.2019, p. 1–19 (BG, ES, CS, DA, DE, ET, EL, EN, FR, GA, HR, IT, LV, LT, HU, MT, NL, PL, PT, RO, SK, SL, FI, SV)

In force

CELEX number:
32019L0904
Author:
European Parliament, Council of the European Union
Date of document:
05/06/2019; Date of signature

Regulation (EC) No 1069/2009 of the European Parliament and of the Council of 21 October 2009 laying down health rules as regards animal by-products and derived products not intended for human consumption and repealing Regulation (EC) No 1774/2002 (Animal by-products Regulation)

OJ L 300, 14.11.2009, p. 1–33 (BG, ES, CS, DA, DE, ET, EL, EN, FR, GA, IT, LV, LT, HU, MT, NL, PL, PT, RO, SK, SL, FI, SV)
This document has been published in a special edition(s) (HR)

In force

CELEX number:
32009R1069
Author:
European Parliament, Council of the European Union
Date of document:
21/10/2009

Directive 98/79/EC of the European Parliament and of the Council of 27 October 1998 on in vitro diagnostic medical devices

OJ L 331, 7.12.1998, p. 1–37 (ES, DA, DE, EL, EN, FR, IT, NL, PT, FI, SV)
This document has been published in a special edition(s) (CS, ET, LV, LT, HU, MT, PL, SK, SL, BG, RO, HR)

In force

CELEX number:
31998L0079
Author:
European Parliament, Council of the European Union
Date of document:
27/10/1998

Directive (EU) 2019/770 of the European Parliament and of the Council of 20 May 2019 on certain aspects concerning contracts for the supply of digital content and digital services (Text with EEA relevance.)

PE/26/2019/REV/1

OJ L 136, 22.5.2019, p. 1–27 (BG, ES, CS, DA, DE, ET, EL, EN, FR, GA, HR, IT, LV, LT, HU, MT, NL, PL, PT, RO, SK, SL, FI, SV)

In force

CELEX number:
32019L0770
Author:
European Parliament, Council of the European Union
Date of document:
20/05/2019; Date of signature

Directive 2011/24/EU of the European Parliament and of the Council of 9 March 2011 on the application of patients’ rights in cross-border healthcare

OJ L 88, 4.4.2011, p. 45–65 (BG, ES, CS, DA, DE, ET, EL, EN, FR, IT, LV, LT, HU, MT, NL, PL, PT, RO, SK, SL, FI, SV)
This document has been published in a special edition(s) (HR)

In force

CELEX number:
32011L0024
Author:
European Parliament, Council of the European Union
Date of document:
09/03/2011

Regulation (EC) No 1394/2007 of the European Parliament and of the Council of 13 November 2007 on advanced therapy medicinal products and amending Directive 2001/83/EC and Regulation (EC) No 726/2004 (Text with EEA relevance)

OJ L 324, 10.12.2007, p. 121–137 (BG, ES, CS, DA, DE, ET, EL, EN, FR, GA, IT, LV, LT, HU, MT, NL, PL, PT, RO, SK, SL, FI, SV)
This document has been published in a special edition(s) (HR)

In force

CELEX number:
32007R1394
Author:
European Parliament, Council of the European Union
Date of document:
13/11/2007
2