- Latest available (Revised)
- Point in Time (31/12/2020)
- Original (As adopted by EU)
When the UK left the EU, legislation.gov.uk published EU legislation that had been published by the EU up to IP completion day (31 December 2020 11.00 p.m.). On legislation.gov.uk, these items of legislation are kept up-to-date with any amendments made by the UK since then.
Legislation.gov.uk publishes the UK version. EUR-Lex publishes the EU version. The EU Exit Web Archive holds a snapshot of EUR-Lex’s version from IP completion day (31 December 2020 11.00 p.m.).
Point in time view as at 31/12/2020.
Commission Decision of 5 December 2006 amending Council Directives 64/432/EEC, 90/539/EEC, 92/35/EEC, 92/119/EEC, 93/53/EEC, 95/70/EC, 2000/75/EC, 2001/89/EC, 2002/60/EC and Decision 2001/618/EC as regards lists of national reference laboratories and State institutes (notified under document number C(2006) 5856) (Text with EEA relevance) (2006/911/EC), Introductory Text is up to date with all changes known to be in force on or before 18 November 2024. There are changes that may be brought into force at a future date. Changes that have been made appear in the content and are referenced with annotations.
Changes and effects yet to be applied by the editorial team are only applicable when viewing the latest version or prospective version of legislation. They are therefore not accessible when viewing legislation as at a specific point in time. To view the ‘Changes to Legislation’ information for this provision return to the latest version view using the options provided in the ‘What Version’ box above.
THE COMMISSION OF THE EUROPEAN COMMUNITIES,
Having regard to the Treaty establishing the European Community,
Having regard to Council Directive 64/432/EEC of 26 June 1964 on animal health problems affecting intra-Community trade in bovine animals and swine(1), and in particular Article 8, Article 9 (2), Article 10 (2) and the second subparagraph of Article 16 (1) thereof,
Having regard to Council Directive 90/539/EEC of 15 October 1990 on animal health conditions governing intra-Community trade in, and imports from third countries of, poultry and hatching eggs(2), and in particular Article 34 thereof,
Having regard to Council Directive 92/35/EEC of 29 April 1992 laying down control rules and measures to combat African horse sickness(3), in particular Article 18 thereof,
Having regard to Council Directive 92/119/EEC of 17 December 1992 introducing general Community measures for the control of certain animal diseases and specific measures relating to swine vesicular disease(4), and in particular Article 24 (2) thereof,
Having regard to Council Directive 93/53/EEC of 24 June 1993 introducing minimum Community measures for the control of certain fish diseases(5), and in particular the second paragraph of Article 18 thereof,
Having regard to Council Directive 95/70/EC of 22 December 1995 introducing minimum Community measures for the control of certain diseases affecting bivalve molluscs(6), and in particular the second paragraph of Article 9 thereof,
Having regard to Council Directive 2000/75/EC of 20 November 2000 laying down specific provisions for the control and eradication of bluetongue(7), and in particular the second paragraph of Article 19 thereof,
Having regard to Council Directive 2001/89/EC of 23 October 2001 on Community measures for the control of classical swine fever(8), and in particular Article 25 (2) thereof,
Having regard to Council Directive 2002/60/EC of 27 June 2002 laying down specific provisions for the control of African swine fever and amending Directive 92/119/EC as regards Teschen disease and African swine fever(9), and in particular Article 26 (1) thereof,
Whereas:
(1) Directive 64/432/EEC sets out a list of State institutes and national reference laboratories responsible for official testing of tuberculins and reagents, a list of national reference laboratories for bovine brucellosis, as well as a list of official institutes responsible for calibrating the standard working antigen of the laboratory against the official EEC standard serum (EI serum) supplied by the State Veterinary Serum Laboratory in Copenhagen, as regards enzootic bovine leucosis.
(2) Directive 90/539/EEC provides for the designation by Member States of national reference laboratories responsible for coordinating diagnostic methods and their use by approved laboratories. The national reference laboratories are listed in that Directive.
(3) Directive 92/35/EEC provides for the designation by Member States of national reference laboratories responsible for coordinating diagnostic methods and their use by approved laboratories. The national reference laboratories are listed in that Directive.
(4) Directive 92/119/EEC provides for the designation by Member States of national laboratories, for each of the diseases referred to in that Directive. The list of national laboratories for swine vesicular disease is set out in that Directive.
(5) Directive 93/53/EEC provides for the designation by Member States of national reference laboratories, for each of the diseases referred to in that Directive. The list of national reference laboratories for fish diseases is set out in that Directive.
(6) Directive 95/70/EC provides for the designation by Member States of national reference laboratories to carry out sampling and testing. The list of national reference laboratories for diseases of bivalve molluscs is set out in that Directive.
(7) Directive 2000/75/EC provides for the designation by Member States of national laboratories responsible for carrying out laboratory tests. Those national laboratories are listed in that Directive.
(8) Directive 2001/89/EC provides that Member States are to ensure that a national laboratory is responsible for coordinating standards and methods of diagnosis. Those national laboratories are listed in that Directive.
(9) Directive 2002/60/EC provides that Member States are to ensure that a national laboratory is responsible for coordinating standards and methods of diagnosis. Those national laboratories are listed in that Directive.
(10) Commission Decision 2001/618/EC of 23 July 2001 on additional guarantees in intra-Community trade of pigs relating to Aujeszky's disease, criteria to provide information on this disease and repealing Decisions 93/24/EEC and 93/244/EEC(10) establishes the list of institutes responsible for checking the quality of the ELISA method in each Member State, and in particular for producing and standardising national reference sera according to the Community reference sera. That list is set out in that Decision.
(11) The competent authorities of almost all Member States submitted requests for updating details concerning national reference laboratories listed in a number of Directives and Decision. In addition, it is appropriate that the national references laboratories and State institutes referred to in those acts are listed in the alphabetic order of the ISO code for each Member State.
(12) In the interests of clarity and consistency of Community legislation, it is appropriate to replace such lists in those Directives and that Decision.
(13) Directives 64/432/EEC, 90/539/EEC, 92/35/EEC, 92/119/EEC, 93/53/EEC, 95/70/EC, 2000/75/EC, 2001/89/EC, 2002/60/EC and Decision 2001/618/EC should therefore be amended accordingly.
(14) The measures provided for in this Decision are in accordance with the opinion of the Standing Committee on the Food Chain and Animal Health,
HAS ADOPTED THIS DECISION:
OJ 121, 29.7.1964, p. 1977/64. Directive as last amended by Regulation (EC) No 1/2005 (OJ L 3, 5.1.2005, p. 1).
OJ L 303, 31.10.1990, p. 6. Directive as last amended by Regulation (EC) No 806/2003 (OJ L 122, 16.5.2003, p. 1).
OJ L 157, 10.6.1992, p. 19. Directive as last amended by the 2003 Act of Accession.
OJ L 62, 15.3.1993, p. 69. Directive as last amended by the 2003 Act of Accession.
OJ L 175, 19.7.1993, p. 23. Directive as last amended by the 2003 Act of Accession.
OJ L 332, 30.12.1995, p. 33. Directive as last amended by Commision Decision 2006/775/EC (OJ L 314, 15.11.2006, p. 33).
OJ L 327, 22.12.2000, p. 74. Directive as amended by the 2003 Act of Accession.
OJ L 316, 1.12.2001, p. 5. Directive as amended by the 2003 Act of Accession.
OJ L 192, 20.7.2002, p. 27. Directive as amended by the 2003 Act of Accession.
OJ L 215, 9.8.2001, p. 48. Decision as last amended by Decision 2005/768/EC (OJ L 290, 4.11.2005, p. 27).
The Whole Decision you have selected contains over 200 provisions and might take some time to download. You may also experience some issues with your browser, such as an alert box that a script is taking a long time to run.
Would you like to continue?
The Schedules you have selected contains over 200 provisions and might take some time to download. You may also experience some issues with your browser, such as an alert box that a script is taking a long time to run.
Would you like to continue?
Latest Available (revised):The latest available updated version of the legislation incorporating changes made by subsequent legislation and applied by our editorial team. Changes we have not yet applied to the text, can be found in the ‘Changes to Legislation’ area.
Original (As adopted by EU): The original version of the legislation as it stood when it was first adopted in the EU. No changes have been applied to the text.
Point in Time: This becomes available after navigating to view revised legislation as it stood at a certain point in time via Advanced Features > Show Timeline of Changes or via a point in time advanced search.
Geographical Extent: Indicates the geographical area that this provision applies to. For further information see ‘Frequently Asked Questions’.
Show Timeline of Changes: See how this legislation has or could change over time. Turning this feature on will show extra navigation options to go to these specific points in time. Return to the latest available version by using the controls above in the What Version box.
Access essential accompanying documents and information for this legislation item from this tab. Dependent on the legislation item being viewed this may include:
This timeline shows the different versions taken from EUR-Lex before exit day and during the implementation period as well as any subsequent versions created after the implementation period as a result of changes made by UK legislation.
The dates for the EU versions are taken from the document dates on EUR-Lex and may not always coincide with when the changes came into force for the document.
For any versions created after the implementation period as a result of changes made by UK legislation the date will coincide with the earliest date on which the change (e.g an insertion, a repeal or a substitution) that was applied came into force. For further information see our guide to revised legislation on Understanding Legislation.
Use this menu to access essential accompanying documents and information for this legislation item. Dependent on the legislation item being viewed this may include:
Click 'View More' or select 'More Resources' tab for additional information including: