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Risk Assessment, Science and Deliberation: Managing Regulatory Diversity under the SPS Agreement?
Published online by Cambridge University Press: 20 January 2017
Abstract
The adoption by WTO Members of measures relating to the protection of health and life of animals, plants and humans is regulated by the WTO Sanitary and Phytosanitary (SPS)Agreement. A fundamental question in the application of this agreement concerns the distinction to be drawn between legitimate regulation and unlawful restriction of trade. This distinction can be difficult to discern, particularly since different communities have different levels of tolerance for risk, which leads to varying national regulatory decisions. This paper critically examines the approach taken to this question in rulings of the WTO dispute settlement panels and Appellate Body, highlighting and analysing three emergent issues:the role attributed to science, the two stage review process adopted and the application of the principle of mutual recognition. The importance of deliberative decision-making inthis context is emphasised, as is the need for recognition and acceptance of the regulatory diversity that this will bring.
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References
1 US- Continued Suspension of Obligations in the EC-Hormones Dispute Report of the Appellate Body WT/DS320/AB/R, adopted 14 November 2008 DSR 2008:X 3507; Canada-Continued Suspension of Obligations in the EC-Hormones Dispute Report of the Appellate Body, WT/DS320/AB/R, adopted 14 November 2008 (references below are to the US Appellate Body Report); Australia – MeasuresAffecting the Importation of Apples from New Zealand, Report of the Appellate Body, WT/DS367/AB/R, 29 November 2010. The implications of this review process will be discussed below.
2 Lawrence Busch, Robin Grove-White, Sheila Jasanoff, David Winickoff, Brian Wynne “Amicus Curiae Brief: Submitted to the Dispute Settlement Panel of the World Trade Organisation in the case of EC: Measures Affecting the Approval and Marketing of Biotech Products” 30 April 2004, at 20.
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9 Article 2.2 SPS. In EC-Biotech the panel observed that there are three prongs to Article 2.2 SPS (measures (i) cannot go beyond what is ‘necessary’, (ii) must be based upon science, and (iii) must be supported by ‘sufficient’ scientific evidence) however on the facts the panel did not examine the question of ‘necessity’, focussing instead upon the questions of the nature and suffi ciency of scientifi c evidence; it is these which have subsequently prompted the greatest discussion. Measures affecting the Approval and marketing of Biotech Products, Report of the Panel WT/DS291–3/R, 29 September 2006, at para. 7.3394. On the potential interpretation of ‘necessity’ see further Scott, Commentary on the Sanitary and Phytosanitary Measures Agreement, supra note 8, at p.85.
10 Note (2) to the SPS Agreement explains that: “… there is a scientifi c justifi cation if, on the basis of an examination and evaluation of available scientifi c information in conformity with the relevant provisions of this Agreement, a Member determines that the relevant international standards, guidelines or recommendations are not sufficient to achieve its appropriate level of sanitary or phytosanitary protection.”
11 Article 5.1 SPS
12 Article 5.2 SPS.
13 Article 5.3 SPS.
14 Article 5.5 SPS.
15 A note to Article 5.6 SPS clarifies that “a measure is not more traderestrictive than required unless there is another measure, reasonably available taking into account technical and economic feasibility, that achieves the appropriate level of sanitary or phytosanitary protection and is significantly less restrictive to trade”.
16 While Annex A.4 SPS provides a definition this relates to the nature of the substantive risks to be evaluated, rather than the process itself: “the evaluation of the likelihood of entry, establishment or spread of a pest or disease within the territory of an importing Member … and of the associated potential biological and economic consequences; or the evaluation of the potential for adverse effects on human or animal health arising from the presence of additives, contaminants, toxins or disease causing organisms in food, beverages or feedstuffs.”
17 European Communities-Measures Concerning Meat and Meat Products (Hormones), Panel Report, WT/DS26/R/USA, WT/DS248/R/ Canada adopted 18 August 1997, at US Panel Report, paras. 8.94– 8.95, Canada Panel report, paras. 8.97–8.98. US- Continued Suspension Panel Report,WT/DS320/R at para. 6.99, Panel Report Canada – Continued Suspension WT/DS321/R at para. 6.91.
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19 EC-Measures Concerning Meat and Meat Products (Hormones), Report of the Appellate Body WT/DS26/AB/R, WT/DS248/AB/R adopted 13 February 1998, DSR 1998:I, 135 at para. 181.
20 Supra note 1 at para. 542.
21 Supra note 19 at para. 115.
22 Ibid. at para. 180
23 Ibid. at para. 117.
24 Ibid. at para. 187.
25 Fisher, Risk Regulation and Administrative Constitutionalism, supra note 3 at p. 189.
26 Australia-Measures Affecting Importation of Salmon, Panel Report, WT/DS18/R, adopted 12 June 1998.
27 Australia-Measures Affecting Importation of Salmon, Report of the Appellate Body, WT/DS18/AB/R, adopted 20 October 1998.
28 Japan-Measures Affecting the Importation of Apples, Report of the Appellate Body, WT/DS245/AB/R, adopted 10 December 2003, DSR 2003: IX, 4391 paras. 162 and 163, referring to Japan-Measures Affecting Agricultural Products II, Report of the Appellate Body WT/DS76/AB/R, adopted 19 March 1999, DSR 1999:I, 277.
29 Japan-Apples, Appellate Body Report, ibid. at para. 164, again referring to Japan–Agricultural Products II, ibid. at para. 84.
30 Continued Suspension, supra note 1.
31 Ibid. at para. 590.
32 Ibid. at para. 591.
33 US-Continued Suspension Appellate Body Report, supra note1 at para. 542.
34 Ibid. at para. 685. “A WTO Member that adopts an SPS measure resulting in a higher level of protection than would be achieved by measures based on international standards must nevertheless ensure that its SPS measure complies with the other requirements of the SPS Agreement, in particular Article 5”.
35 Ibid. at para 592.
36 Ibid.
37 Ibid.
38 See below.
39 Australia-Apples, supra note 1.
40 Australia's Appellant's submission para 76, quoted at para. 22, Appellate Body Report, ibid. (emphasis in original).
41 Australia-Apples, Appellate Body Report ibid. at para. 220.
42 Ibid. at para. 222.
43 Ibid. at para. 224.
44 US-Continued Suspension Appellate Body Report, supra note 1.
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58 US-Continued Suspension Appellate Body Report, supra note 1 at para. 590, emphasis added.
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62 See text accompanying note 8.
63 Such justification can only be on the grounds of a specifi ed (exhaustive) list of objectives (including human animal or plant health) (Article 36 TFEU) or, for “indistinctly applicable” measures only (those which apply to both imported and domestically produced products without distinction) by reference to a “mandatory requirement”, that is an over-riding public policy objective or value (demonstrably of particular signifi cance to the regulating state.) See Case 120/78 Rewe Zentral AG v. Bundesmonopolverwaltung für Branntwein (Cassis de Dijon) [1979] ECR 649. See further Barnard, Catherine, EU Substantive Law, 3rd Ed. (Oxford: Oxford University Press 2010).Google Scholar
64 This is not to suggest that the Appellate Body could or should follow the ECJ's example in its interpretative approach. The Appellate Body does not have the same interpretative role as the ECJ (and the WTO does not have the same objectives as the EU) and questions would arise relating to the AB's (lack of) mandate were it to seek to apply an activist interpretative approach.
65 Fisher, Risk Regulation and Administrative Constitutionalism, supra note 3, at 178–9.
66 See Opinion of Advocate General Tesauro in Case C-292/92 Hunermund v. Landesapthekerkammer [1993] ECR I-6787; Opinion of Advocate General Maduro in Case C-158/04 Alfa Vita Vassilopoulos (Trofo Super-Markets) [2006] I-8135, paras 43–45.
67 See Reid, Emily, “Regulatory Autonomy in the EU and WTO: Defining and Defending its Limits”, 44 Journal of World Trade (2010), pp. 977 et sqq.Google Scholar