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EPA Review Annex Documents - DFID

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Specific provisions<br />

While the final and interim agreements share a considerable amount of common language,<br />

they differ significantly in the range and scope of their specific provisions. Broadly, where<br />

specific provisions have been agreed, the language tends to be rather vague and noncommittal,<br />

the final agreement between the EC and CARIFORUM is testament to this point<br />

(ECLAC, 2008). At the same time, there are some notable instances where specific<br />

provisions, for example related to equivalence or regional harmonisation are given more<br />

prominence and/or make firmer commitments.<br />

Competent Authority<br />

The EU’s approach to the control of food safety in imports of food and feed from Third<br />

Countries has increasingly relied on the recognition of an approved component authority in<br />

the exporting country. Such a system has been in place for some time in the case of food of<br />

animal origin and for phytosanitary controls (European Commission, 2006). While, imports of<br />

many foods of non-animal origin are not subject to controls by an approved component<br />

authority, it is evident that Regulation (EC) 882/2004 puts greater emphasis on the ability of<br />

Third Countries to demonstrate that their food controls are equivalent to those in the EU and<br />

provides for the inspection of these systems by the European Commission. This suggests<br />

that component authorities in Third Countries will play an increasing role for exports to the<br />

EU of all food and feed products.<br />

All of the final or interim agreements make reference to a designated competent authority for<br />

the implementation of SPS measures, that the parties are required to specify and<br />

communicate to each other. The component authority is charged with the implementation of<br />

the measures defined in the <strong>EPA</strong>, as they apply to SPS measures.<br />

Regionalisation<br />

Article 6 of the SPS Agreement specifies that WTO Members must adapt their SPS<br />

measures to reflect the area from which a product is originated and/or to which it is destined,<br />

whether a country in its entirety or only part of a country. Specifically, they must recognise<br />

the concepts of pest- or disease-free areas and areas of low pest- or disease-prevalence<br />

and adapt their SPS measures accordingly. This requirement is typically referred to as<br />

‘regionalisation’.<br />

In assessing the characteristics of a particular region, WTO Members must take into account<br />

the level of prevalence of specific diseases or pests, the existence of eradication or control<br />

programmes and appropriate criteria or guidelines developed by relevant international<br />

organisations. In 2008, the SPS Committee adopted guidelines to facilitate the recognition<br />

of pest- or disease-free areas. 163 Critically, under the SPS Agreement the onus is on<br />

exporting countries to provide the necessary evidence in order to demonstrate objectively to<br />

importing countries that particular regions are free of pertinent pests or diseases and are<br />

likely to remain that way. Importing countries must be permitted reasonable access to<br />

undertake inspections, testing and the like to confirm conditions in the area.<br />

A number of the interim agreements, namely between the EU and Ghana, Cote d’ Ivoire,<br />

Central Africa and SADC, make reference to the concept of regionalisation, although<br />

referring to it as ‘zoning’. For example, Article 60 Part 4 of the SADC interim agreement<br />

specifies:<br />

163 Document G/SPS/48.<br />

238

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