Search Legislation

Regulation (EC) No 999/2001 of the European Parliament and of the CouncilShow full title

Regulation (EC) No 999/2001 of the European Parliament and of the Council of 22 May 2001 laying down rules for the prevention, control and eradication of certain transmissible spongiform encephalopathies

 Help about what version

What Version

 Help about advanced features

Advanced Features

 Help about UK-EU Regulation

Legislation originating from the 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.

Close

This item of legislation originated from the EU

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.).

Status:

Point in time view as at 01/01/2019.

Changes to legislation:

There are currently no known outstanding effects for the Regulation (EC) No 999/2001 of the European Parliament and of the Council, CHAPTER A . Help about Changes to Legislation

Close

Changes to Legislation

Revised legislation carried on this site may not be fully up to date. At the current time any known changes or effects made by subsequent legislation have been applied to the text of the legislation you are viewing by the editorial team. Please see ‘Frequently Asked Questions’ for details regarding the timescales for which new effects are identified and recorded on this site.

[F1CHAPTER A U.K. National reference laboratories

1.

The designated national reference laboratory is to:

(a)

have at its disposal facilities and expert personnel enabling it to show at all times, and especially when the disease in question first appears, the type and strain of the agent of TSE, and to confirm results obtained by official diagnostic laboratories. Where it is not capable of identifying the strain-type of the agent, it shall set up a procedure to ensure that the identification of the strain is referred to the EU reference laboratory;

(b)

verify diagnostic methods used in official diagnostic laboratories;

(c)

be responsible for coordination of diagnostic standards and methods within the Member State. To this end, it:

  • may provide diagnostic reagents to official diagnostic laboratories;

  • is to control the quality of all diagnostic reagents used in the Member State

  • is to periodically arrange comparative tests

  • is to hold isolates of the agents of the disease in question, or corresponding tissues containing such agents, coming from cases confirmed in the Member State

  • is to ensure confirmation of results obtained in diagnostic laboratories;

(d)

is to cooperate with the EU reference laboratory, which includes the participation in the periodic comparative tests organised by the EU reference laboratory. Should a national reference laboratory fail in a comparative test organised by the EU reference laboratory, it shall take immediately all the corrective actions to remedy the situation and successfully pass the repeat comparative test or the next comparative test organised by the EU reference laboratory.

2.

However, by way of derogation from point 1, Member States which do not have a national reference laboratory shall use the services of the EU reference laboratory or of national reference laboratories located in other Member States or European Free Trade Association (EFTA) Members.

3.

The national reference laboratories are:

Austria:

Agentur für Gesundheit und Ernährungssicherheit GmbH (AGES) Institut für veterinärmedizinische Untersuchungen

Robert Koch Gasse 17

A-2340 Mödling

Belgium:

CERVA-CODA-VAR

Centre d'Étude et de Recherches Vétérinaires et Agrochimiques, Centrum voor Onderzoek in Diergeneeskunde en Agrochemie, Veterinary and Agrochemical Research Centre

Groeselenberg 99

B-1180 Bruxelles

Bulgaria:

Национален диагностичен научноизследователски ветеринарномедицински институт Проф. Д-р Георги Павлов

Национална референтна лаборатория Трансмисивни спонгиформни енцефалопатии

бул. Пенчо Славейков 15

София 1606

( National Diagnostic Veterinary Research Institute ‘Prof. Dr Georgi Pavlov’, National Reference Laboratory for Transmissible Spongiform Encephalopathies, 15 Pencho Slaveykov Blvd., 1606 Sofia )

Croatia:

Hrvatski veterinarski institut,

Savska Cesta 143

10000 Zagreb

Cyprus:

State Veterinary Laboratories

Veterinary Services

CY-1417 Athalassa

Nicosia

Czech Republic:

Státní veterinární ústav Jihlava (State Veterinary Institute Jihlava)

National Reference Laboratory for BSE and Animal TSEs

Rantířovská 93

586 05 Jihlava

Denmark:

Veterinærinstituttet

Danmarks Tekniske Universitet

Bülowsvej 27

DK-1870 Frederiksberg C

( National Veterinary Institute, Technical University of Denmark, 27, Bülowsvej, DK — 1870 Frederiksberg C )

Estonia:

Veterinaar- ja Toidulaboratoorium (Estonian Veterinary and Food Laboratory)

Kreutzwaldi 30

Tartu 51006

Finland:

Finnish Food Safety Authority Evira

Research and Laboratory Department

Veterinary Virology Research Unit- TSEs

Mustialankatu 3

FI-00790 Helsinki

France:

ANSES-Lyon, Unité MND

31, avenue Tony Garnier

69 364 LYON Cedex 07

Germany:

Friedrich-Loeffler-Institut

Institute for Novel and Emerging Infectious Diseases at the Friederich-Loeffler-Institut

Federal Research Institute for Animal Health

Suedufer 10

D-17493 Greifswald Insel Riems

Greece:

Ministry of Agriculture — Veterinary Laboratory of Larissa

6th km of Larissa — Trikala Highway

GR-41110 Larissa

Hungary:

Veterinary Diagnostic Directorate, National Food Chain Safety Office (VDD NFCSO)

Tábornok u. 2

1143 Budapest

Ireland:

Central Veterinary Research Laboratory

Department of Agriculture, Food and the Marine

Backweston Campus

Celbridge

Co. Kildare

Italy:

Istituto Zooprofilattico Sperimentale del Piemonte, Liguria e Valle d'Aosta — CEA

Via Bologna, 148

I-10154 Torino

Latvia:

Institute of Food Safety, Animal Health and Environment (BIOR)

Lejupes Str. 3

Riga LV 1076

Lithuania:

National Food and Veterinary Risk Assessment Institute

J. Kairiūkščio str. 10

LT-08409 Vilnius

Luxembourg:

CERVA-CODA-VAR

Centre d'Étude et de Recherches Vétérinaires et Agrochimiques, Centrum voor Onderzoek in Diergeneeskunde en Agrochemie, Veterinary and Agrochemical Research Centre

Groeselenberg 99

B-1180 Bruxelles

Malta:

Veterinary Diagnostic Laboratory

Department of Food Health and Diagnostics

Veterinary Affairs and Fisheries Division

Ministry for Rural Affairs and the Environment

Albert Town Marsa

Netherlands:

Central Veterinary Instutute of Wageningen UR

Edelhertweg 15

8219 PH Lelystad

P.O. Box 2004

NL-8203 AA Lelystad

Poland:

Państwowy Instytut Weterynaryjny (PIWet)

24-100 Puławy

al. Partyzantów 57

Portugal:

Setor diagnóstico EET

Laboratório de Patologia

Unidade Estratégica de Investigação e Serviços de Produção e Saúde Animal

Instituto Nacional de Investigação Agrária e Veterinária Rua General Morais Sarmento

1500-311 Lisboa

Romania:

Institutul de Diagnostic și Sănătate Animală (Institute for Diagnosis and Animal Health)

Department of Morphology

Strada Dr Staicovici nr. 63, 5

București 050557

Slovakia:

State Veterinary Institute Zvolen

Pod dráhami 918

SK-960 86, Zvolen

Slovenia:

University of Ljubljana, Veterinary faculty

National Veterinary Institute

Gerbičeva 60

SI-1000 Ljubljana

Spain:

Laboratorio Central de Veterinaria (Algete)

Ctra. M-106 pk 1,4

28110 Algete (Madrid)

Sweden:

National Veterinary Institute

S-751 89 Uppsala

United Kingdom:

Animal Health and Veterinary Laboratories Agency

Woodham Lane

New Haw, Addlestone, Surrey KT15 3NB]

Back to top

Options/Help

Print Options

You have chosen to open the Whole Regulation

The Whole Regulation 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?

You have chosen to open Schedules only

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?

Close

Legislation is available in different versions:

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.

Close

See additional information alongside the content

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.

Close

Opening Options

Different options to open legislation in order to view more content on screen at once

Close

More Resources

Access essential accompanying documents and information for this legislation item from this tab. Dependent on the legislation item being viewed this may include:

  • the original print PDF of the as adopted version that was used for the EU Official Journal
  • lists of changes made by and/or affecting this legislation item
  • all formats of all associated documents
  • correction slips
  • links to related legislation and further information resources
Close

Timeline of Changes

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.

Close

More Resources

Use this menu to access essential accompanying documents and information for this legislation item. Dependent on the legislation item being viewed this may include:

  • the original print PDF of the as adopted version that was used for the print copy
  • correction slips

Click 'View More' or select 'More Resources' tab for additional information including:

  • lists of changes made by and/or affecting this legislation item
  • confers power and blanket amendment details
  • all formats of all associated documents
  • links to related legislation and further information resources