ALINORM 03/26/1 - codex - BSN
ALINORM 03/26/1 - codex - BSN
ALINORM 03/26/1 - codex - BSN
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18 REP12/CAC<br />
disruption to trade. They highlighted their concerns on the long delay to adopt the MRLs based on nonscientific<br />
factors and stressed the need for Codex to base its decisions on science, in view of the status of<br />
Codex standards under the WTO SPS Agreement. They recalled that failure to adopt the MRLs for<br />
ractopamine could negatively impact on food security as the establishment of MRLs for ractopamine would<br />
allow the safe use of new technologies to meet the increasing demand for food production foreseen by FAO.<br />
One delegation pointed out that <strong>26</strong> countries were using ractopamine without problems and that no technical<br />
barriers to trade or food safety alerts through INFOSAN had been reported due to its use.<br />
101. The JECFA Secretariat clarified that ractopamine had been evaluated on several occasions and an ADI<br />
had been established and MRLs proposed that are compatible with consumer safety. Additional residue<br />
studies in pig lungs had been evaluated based on request of the Commission and the report was published<br />
and considered at the 34 th CAC. If safety concerns were brought forth regarding ractopamine, these needed to<br />
be supported by data.<br />
102. After an extensive debate, which had essentially reproduced the discussion that took place at the 34 th<br />
CAC about the three main options on the way to proceed (i.e. continue to hold the draft MRLs at Step 8;<br />
discontinue work on the draft MRLs; and vote on the adoption of the draft MRLs) and their rationale, a large<br />
number of delegations and two observers continued to request the floor. Therefore, the Chairperson proposed,<br />
in view of time constraints, to interrupt the general discussion and to focus on how to move forward.<br />
1<strong>03</strong>. The Chairperson noted that the Commission had not found consensus and noted that as per Rule XII.2<br />
of the Rules of the Procedure of the Codex Alimentarius Commission, the Commission should make every<br />
effort to reach consensus on the adoption or amendment of standards by consensus. The Chairperson noted<br />
that the Procedural Manual provided sufficient guidance through the Working Principles for Risk Analysis for<br />
Application in the Framework of the Codex Alimentarius Commission, the Risk Analysis Principles Applied<br />
by the CCRVDF and the Statements of Principles Concerning the Role of Science in the Codex Decision-<br />
Making Process and the Extent to which other Factors are Taken into Account.<br />
104. The Delegation of Ghana was of the view that, according to Rule XII.2 “consensus” was not a must<br />
but rather a preference for Codex. Therefore, the Delegation called for a roll-call-vote on the adoption of the<br />
draft MRLs for ractopamine as, in their view, all seven “Measures to Facilitate Consensus” had been<br />
explored.<br />
105. The Chairperson raised the question whether every effort had been made to reach consensus before<br />
proceeding with such a vote, as required by the Rule XII.2<br />
106. Delegations were split among:<br />
(i) those who considered that not all measures had been exhausted and, in particular, the following<br />
required further efforts:<br />
- Refraining from submitting proposals in the step process where the scientific basis is not well<br />
established on current data and, where necessary, carry out further studies in order to clarify<br />
controversial issues.<br />
- Providing that matters are not progressed from step to step until all relevant concerns are taken<br />
into account and adequate compromises worked out.<br />
- Emphasizing to Committees and their Chairpersons that matters should not be passed on to the<br />
Commission until such time as consensus has been achieved at the technical level.<br />
In their view, not all scientific evidence had been fully explored; the CCRVDF had prematurely<br />
forwarded the draft MRLs to the Commission without having achieved consensus at the technical level.<br />
(ii) those who considered that all efforts to reach consensus had been made. They were of the view<br />
that: JECFA had clarified that all relevant data had been considered in their recommendations; that<br />
the CCRVDF had in fact considered all relevant concerns and those concerns that were not<br />
addressed were not scientific concerns; and that the Chairperson of the CCRVDF had followed the<br />
Guidelines to the Chairperson of Codex Committees to achieve consensus at the technical level but<br />
no consensus could be found.