X
XLinkedinWhatsAppTelegramTelegram
0
Read this article in:

Statement by the EU on ractopamine

Following vote at the Codex Alimentarius, the European Union reaffirms its position that an international standard for ractopamine is not justified.

9 July 2012
X
XLinkedinWhatsAppTelegramTelegram
0

Following vote at the Codex Alimentarius, the European Union reaffirms its position that an international standard for ractopamine is not justified.

The European Union remains strongly opposed to the adoption of maximum residue limits (MRLs) for the growth promoting substance, ractopamine, in pigs and cattle as there remain outstanding safety concerns.

The European Union's risk assessment body, the European Food Safety Authority, has concluded that there is insufficient data upon which to make a proposal for MRLs for ractopamine and that thereby risks to human health cannot be ruled out. Given its outstanding safety concerns, the European Union's current legislation will remain in place.

The European Union, together with other European countries, numbering close to 45 countries, was supported by an overwhelming number of some of the world's most populous nations, namely: China, the Russian Federation, India, Turkey, Iran, Egypt, Kenya, Zimbabwe and others. These countries indicated that they too will maintain their positions and not approve the use of this growth promoting substance.

The European Union believes that the decision-making process that led to this result is regrettable. The decision was taken on the basis of a single vote difference. As an international organisation seeking to harmonise standards across the globe, Codex should respect consensus-based decision-making, one of the fundamental principles of the organisation. It is clear that for standards to be universally applicable, they also need to be universally accepted. The European Commission represented EU interests at the 35th session of the annual Codex Alimentarius Commission which is taking place from 2-7 July 2012 in Rome. Bringing together 185 member countries, Codex's aim was to adopt internationally accepted standards on food safety and food quality.

Friday July 6, 2012/ European Commission/ European Union.
http://europa.eu/

Article Comments

This area is not intended to be a place to consult authors about their articles, but rather a place for open discussion among pig333.com users.
Leave a new Comment

Access restricted to 333 users. In order to post a comment you must be logged in.

You are not subscribed to this list Swine News

Swine industry news in your email

Log in and sign up on the list

Related articles

UN food safety body sets limits on ractopamine

09-Jul-2012
The Commission set the limits for the amount of ractopamine allowed in the tissues of pigs and cattle at 10 micrograms per kilogram of pig or cattle muscle, 40 micrograms per kilogram in liver and 90 micrograms per kilogram of the animals' kidneys.

EU - EFSA evaluates safety of Ractopamine in feed

08-Apr-2009
EFSA’s FEEDAP Panel has just published an opinion on the safety of ractopamine, a growth promoter used in animal feed in some countries outside the EU. EFSA’s FEEDAP Panel found weaknesses in the data underlying the JECFA assessment which would undermine any proposal for a maximum residue level for ractopamine. The Panel found that the study on cardiovascular effects in humans cannot be taken as a basis to derive an Acceptable Daily Intake (ADI) of 0-1 micrograms per kilogramme of body weight per day as proposed by JECFA. EFSA consulted the Community Reference Laboratory responsible for beta-agonists and the European Medicines Agency (EMEA) and included the results of this process in its final opinion.