Decision 1999/879 - 1999/879/EC: Council Decision of 17 December 1999 concerning the placing on the market and administration of bovine somatotrophin (BST)

Please note

This page contains a limited version of this dossier in the EU Monitor.

1.

Current status

This decision has been published on December 23, 1999, entered into force on January  1, 2000 and should have been implemented in national regulation on December 23, 1999 at the latest.

2.

Key information

official title

1999/879/EC: Council Decision of 17 December 1999 concerning the placing on the market and administration of bovine somatotrophin (BST) and repealing Decision 90/218/EEC
 
Legal instrument Decision
Number legal act Decision 1999/879
Original proposal COM(1999)544 EN
CELEX number i 31999D0879

3.

Key dates

Document 17-12-1999
Publication in Official Journal 23-12-1999; Special edition in Slovenian: Chapter 03 Volume 028,Special edition in Maltese: Chapter 03 Volume 028,Special edition in Latvian: Chapter 03 Volume 028,OJ L 331, 23.12.1999,Special edition in Lithuanian: Chapter 03 Volume 028,Special edition in Bulgarian: Chapter 03 Volume 030,Special edition in Croatian: Chapter 03 Volume 060,Special edition in Czech: Chapter 03 Volume 028,Special edition in Estonian: Chapter 03 Volume 028,Special edition in Polish: Chapter 03 Volume 028,Special edition in Hungarian: Chapter 03 Volume 028,Special edition in Slovak: Chapter 03 Volume 028,Special edition in Romanian: Chapter 03 Volume 030
Effect 23-12-1999; Takes effect Date notif.
01-01-2000; Takes effect See Art 5
End of validity 31-12-9999
Notification 23-12-1999; {titleAndReference.draft.disclaimer.new|http://publications.europa.eu/resource/authority/fd_365/titleAndReference.draft.disclaimer.new}

4.

Legislative text

Avis juridique important

|

5.

31999D0879

1999/879/EC: Council Decision of 17 December 1999 concerning the placing on the market and administration of bovine somatotrophin (BST) and repealing Decision 90/218/EEC

Official Journal L 331 , 23/12/1999 P. 0071 - 0072

COUNCIL DECISION

of 17 December 1999

concerning the placing on the market and administration of bovine somatotrophin (BST) and repealing Decision 90/218/EEC

(1999/879/EC)

THE COUNCIL OF THE EUROPEAN UNION,

Having regard to the Treaty establishing the European Community, and in particular Article 37 thereof,

Having regard to the proposal from the Commission,

Having regard to the opinion of the European Parliament(1),

Having regard to the opinion of the Economic and Social Committee(2),

Whereas:

  • (1) 
    Council Decision 90/218/EEC of 25 April 1990 concerning the placing on the market and administration of bovine somatotrophin (BST)(3), provides in Article 1 that Member States are to ensure that, until 31 December 1999, the placing on the market of bovine somatotrophin for the purposes of its marketing and the administration thereof on their territory to dairy cows by any means whatsoever will not be authorised;
  • (2) 
    By virtue of Article 2(2) of that Decision, the Council instructed the Commission to entrust a Working Party of independent scientists, in collaboration with Member States, with the task of assessing the effects of using BST, taking account of the opinion of the Committee for Veterinary Medicinal Products, in particular as regards the impact of the use of this product on the cases of mastitis;
  • (3) 
    Article 2(1) of that Decision allowed the Member States to carry out limited practical tests on the use of bovine somatotrophin, under the control of an official veterinarian, in order to obtain any other scientific data that may be taken into account by the Council when it takes a final decision. The Commission has not received any information on such tests and in view of the prohibition laid down in this Decision there is no need to continue authorising further such tests;
  • (4) 
    The Protocol on protection and welfare of animals annexed to the Treaty calls on the Community and the Member States, when formulating and implementing the Community's agricultural policy, to pay full regard to the health and welfare requirements of animals;
  • (5) 
    By Decision 78/923/EEC(4), the Community has approved the European Convention for the Protection of Animals Kept for Farming Purposes (hereinafter called "the Convention") and has deposited its instrument of approval; all Member States have also ratified this Convention;
  • (6) 
    Council Directive 98/58/EC of 20 April 1998 concerning the protection of animals kept for farming purposes(5) states in point 18 of the Annex that no other substance, with exception of those given for therapeutic or prophylactic purposes, are to be administered to an animal unless it has been demonstrated by scientific studies of animal welfare or established experience that the effect of the substance is not detrimental to the health or welfare of the animal;
  • (7) 
    BST is not produced to be used in cattle for therapeutic purposes, but only to enhance milk production;
  • (8) 
    The Scientific Committee on Animal Health and Animal Welfare (SCAWAH) adopted on 10 March 1999 its report on Animal Welfare Aspects of the Use of bovine somatotrophin and stated that BST increases the risk of clinical mastitis as well as the duration of treatment of mastitis, that it increases the incidence of foot and leg disorders and that it can affect adversely reproduction as well as induce severe reactions at the injection site;
  • (9) 
    It is important for the health and productivity of dairy cattle that they are subjected to minimum stress which may lead to increase in diseases such as mastitis, foot lesions and reactions to injection site...

More

This text has been adopted from EUR-Lex.

6.

Original proposal

 

7.

Sources and disclaimer

For further information you may want to consult the following sources that have been used to compile this dossier:

This dossier is compiled each night drawing from aforementioned sources through automated processes. We have invested a great deal in optimising the programming underlying these processes. However, we cannot guarantee the sources we draw our information from nor the resulting dossier are without fault.

 

8.

Full version

This page is also available in a full version containing the summary of legislation, the legal context, de Europese rechtsgrond, other dossiers related to the dossier at hand and finally the related cases of the European Court of Justice.

The full version is available for registered users of the EU Monitor by ANP and PDC Informatie Architectuur.

9.

EU Monitor

The EU Monitor enables its users to keep track of the European process of lawmaking, focusing on the relevant dossiers. It automatically signals developments in your chosen topics of interest. Apologies to unregistered users, we can no longer add new users.This service will discontinue in the near future.