Undo information

Time Operation User
05/11/2019 11:27:31 UPDATE peifer
Table Sub# Column Undo Value Current Value
T_SOURCE 0 ABSTRACT The biocidal products directive aims to harmonise the European market for biocidal products and their active substances. Active substances have to be assessed and the decision on their inclusion into Annex I of the Directive shall be taken at Community level. Member States shall authorise the biocidal products in accordance with the rules and procedures set in the Directive. A biocidal product authorised in one Member State shall also be authorised upon application in other Member States unless there are specific grounds to derogate from this principle of mutual recognition. The Directive has been amended by: -Regulation 1882/2003/EC of the European Parliament and of the Council of 29 September 2003 adapting to Council Decision 1999/468/EC (Celex N°31999D0468) the provisions relating to committees which assist the Commission in the exercise of its implementing powers laid down in instruments subject to the procedure referred to in Article 251 of the EC Treaty. -Commission Directive 2006/50/EC of 29 May 2006 amending Annexes IVA and IVB to Directive 98/8/EC of the European Parliament and of the Council concerning the placing of biocidal products on the market. -Commission Directive 2006/140/EC of 20 December 2006 amending Directive 98/8/EC of the European Parliament and of the Council to include sulfuryl fluoride as an active substance in Annex I thereto. -Commission Directive 2007/20/EC of 3 April 2007 amending Directive 98/8/EC of the European Parliament and of the Council to include dichlofluanid as an active substance in Annex I thereto. The biocidal products directive aims to harmonise the European market for biocidal products and their active substances. Active substances have to be assessed and the decision on their inclusion into Annex I of the Directive shall be taken at Community level. Member States shall authorise the biocidal products in accordance with the rules and procedures set in the Directive. A biocidal product authorised in one Member State shall also be authorised upon application in other Member States unless there are specific grounds to derogate from this principle of mutual recognition. The Directive has been amended by: -Regulation 1882/2003/EC of the European Parliament and of the Council of 29 September 2003 adapting to Council Decision 1999/468/EC (Celex N°31999D0468) the provisions relating to committees which assist the Commission in the exercise of its implementing powers laid down in instruments subject to the procedure referred to in Article 251 of the EC Treaty. -Commission Directive 2006/50/EC of 29 May 2006 amending Annexes IVA and IVB to Directive 98/8/EC of the European Parliament and of the Council concerning the placing of biocidal products on the market. -Commission Directive 2006/140/EC of 20 December 2006 amending Directive 98/8/EC of the European Parliament and of the Council to include sulfuryl fluoride as an active substance in Annex I thereto. -Commission Directive 2007/20/EC of 3 April 2007 amending Directive 98/8/EC of the European Parliament and of the Council to include dichlofluanid as an active substance in Annex I thereto.
T_SOURCE 0 ALIAS Biocidal products Directive (consolidated) Biocidal products Directive (consolidated)
T_SOURCE 0 CELEX_REF 31998L0008 (32003R1882, 32006L0050, 32006L0140, 32007L0020) 31998L0008 (32003R1882, 32006L0050, 32006L0140, 32007L0020)
T_SOURCE 0 COMMENT Besides the reporting obligations included here, Member States have a number of obligations for informing the Commission and other Member States as part of the procedures for evaluation and authorization of biocidal products. The first and second phases of the review programme referred to in Article 16(2) have been established in amendments to the directive: Commission Regulation (EC) No 1896/2000, Commission Regulation (EC) No 1687/2002, Commission Regulation (EC) No 2032/2003, Commission Regulation (EC) No 1048/2005 and Commission Regulation (EC) No 1849/2006. Besides the reporting obligations included here, Member States have a number of obligations for informing the Commission and other Member States as part of the procedures for evaluation and authorization of biocidal products. The first and second phases of the review programme referred to in Article 16(2) have been established in amendments to the directive: Commission Regulation (EC) No 1896/2000, Commission Regulation (EC) No 1687/2002, Commission Regulation (EC) No 2032/2003, Commission Regulation (EC) No 1048/2005 and Commission Regulation (EC) No 1849/2006. ======= Date of end of validity: 31/08/2013. Repealed by Regulation (EU) No 528/2012 of the European Parliament and of the Council of 22 May 2012.
T_SOURCE 0 EC_ACCESSION
T_SOURCE 0 EC_ENTRY_INTO_FORCE
T_SOURCE 0 FK_CLIENT_ID 12 12
T_SOURCE 0 FK_TYPE_ID 0 0
T_SOURCE 0 ISSUED_BY
T_SOURCE 0 ISSUED_BY_URL http://ec.europa.eu/environment/biocides/index.htm
T_SOURCE 0 LAST_MODIFIED 2019-11-05 00:00:00.0
T_SOURCE 0 LAST_UPDATE 2007-09-07 11:24:27.0
T_SOURCE 0 LEGAL_NAME 587
T_SOURCE 0 PK_SOURCE_ID 587
T_SOURCE 0 SECRETARIAT
T_SOURCE 0 SECRETARIAT_URL 98/8/EC
T_SOURCE 0 SOURCE_CODE 98/8/EC Y
T_SOURCE 0 TERMINATE Directive 98/8/EC of the European Parliament and of the Council of 16 February 1998 concerning the placing of biocidal products on the market as amended by Council Regulation 1882/2003/EC) and Commission Directives 2006/50/EC, 2006/140/EC and 2007/20/EC
T_SOURCE 0 TITLE Directive 98/8/EC of the European Parliament and of the Council of 16 February 1998 concerning the placing of biocidal products on the market as amended by Council Regulation 1882/2003/EC) and Commission Directives 2006/50/EC, 2006/140/EC and 2007/20/EC http://eur-lex.europa.eu/LexUriServ/site/en/consleg/1998/L/01998L0008-20070119-en.pdf
T_SOURCE 0 URL http://eur-lex.europa.eu/LexUriServ/site/en/consleg/1998/L/01998L0008-20070119-en.pdf 1998-05-14 00:00:00.0
T_SOURCE 0 VALID_FROM 1998-05-14 00:00:00.0