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Complaint by Canada Report of the Panel (Continued)
IV.334 Canada argued that given
that beef containing residues of antimicrobial growth promoters
and other veterinary drugs was widely available in the EC market,
it would not be appropriate, in determining the "likeness"
of Canadian and EC beef, to limit the comparison of beef produced
with growth promoting hormones to beef from cattle that were raised
without the use of antimicrobial growth promoters and other veterinary
drugs. Canada had shown (see paragraph 4.259) that the use
of antimicrobial growth promoters and other veterinary drugs in
the European Communities resulted in the presence of residues
in beef sold there. The presence of antibiotic and sulphonamide
residues, as well as other residues in meat, had been confirmed
in the Communication from the EC Commission to the EC Council.
The European Communities themselves, in their grading system
of beef, did not distinguish between beef produced with and without
growth hormones, or between beef with residues of antimicrobial
growth promoters and other veterinary drugs and that without.
IV.335 Canada submitted that
given the other residues present in beef produced in the European Communities,
Canadian beef produced with the six growth promoting hormones
at issue was a "like product" within the meaning of
Article III:4 of the GATT as compared to beef produced in
the European Communities; and that Canadian beef had been accorded
treatment that was less favourable than EC beef, in contravention
of Article III:4 of the GATT.
IV.336 The European Communities
argued that the measures at issue had their domestic counterpart
in the prohibition on the administration of the same types of
hormones to animals reared in the European Communities and in
the prohibition on the marketing of those animals and of meat
from those animals. The measures applied to domestic products
had identical scope and were subject to the same exceptions as
the measures applied to the imported products. The only difference
between the measures applied to domestic products and those applied
to imported products was that while the former were applied at
the stage of production and sale, the latter were enforced at
the point of importation. Furthermore, the measures applied to
both domestic and imported products as "products",
even if their scope was defined in terms of processes and production
methods ("PPMs") rather than in terms of product characteristics.
The present case was to be distinguished from the situation considered
by the panel report on "US - Restrictions on Imports of Tuna
I", in which the panel had reasoned that the Note ad Article III
covered only those measures which were "applied to products
as such". Yet, according to the panel, the US internal regulations
"could not possibly affect tuna "as a product".251
In contrast, in the present case the reason for prohibiting the
importation of animals which had been treated with certain hormones,
and of meat from those animals (as well as their domestic production
and sale) was precisely that this treatment, unlike the PPMs for
fishing tuna prescribed by the US regulations, modified the physical
characteristics and biological composition of the products.
IV.337 The European Communities
disagreed with the Canadian interpretation of "like products".
In the EC view, a determination of "likeness" must
be exclusively based on objective criteria related to the characteristics
of the products. The purpose of a regulatory distinction between
"like products" might only become relevant in deciding
whether a measure which was inconsistent with Article III:4
could be justified under any of the general exceptions provided
for under Article XX of the GATT. The European Communities
contended that the purpose of the measures at issue was not to
afford protection to domestic production but to protect human
and animal health, as well as the interests of consumers and,
therefore, would not, in conformity with the Canada's own test,
infringe Article III:4. Although two products need not
be identical in order to be "like" for the purposes
of Article III, previous panel reports had taken a consistently
narrow approach when interpreting this term. In "EC - Measures
on Animal Feed Proteins", the panel had rejected a claim
by the United States to the effect that all products used for
the purpose of adding proteins to animal feeds were "like".
The panel noted, inter alia, that the products concerned
had different protein contents and different origins (vegetal,
animal or synthetic).252 More recently, the panel report on "Japan
- Taxes on Alcoholic Beverages", a case concerning the application
of Article III:2, had concluded that:
IV.338 The European Communities
reaffirmed its views that meat from animals to which had been
administered any of the six hormones at issue for growth promotion
had substantially different properties, composition and appearance
than meat from animals to which those hormones had not been administered
or to which they had been administered only for therapeutic purposes.
Moreover, meat from treated animals was perceived by EC consumers
as a distinct product. For these reasons, animals treated with
hormones for growth promotion, and meat from those animals, could
not, in light of the criteria used by previous panel reports,
be considered as "like" to other animals, and meat from
those animals, for the purposes of Article III:4.
IV.339 The European Communities
added that meat from animals treated with any of the hormones
at issue for growth promotion was different from meat from untreated
animals or from animals treated for therapeutical purposes in
several ways. First, the precise mode of action of the prohibited
hormones was not yet understood. It could not be excluded, on
the basis of the available scientific evidence, that they might
act as genotoxic agents that induced permanent genetic mutations
in those animals to which they were administered. The presence
of residues which were potentially genotoxic rendered the meat
unfit for human consumption. Meat which from the sanitary point
of view was not allowed to be consumed and hormone-free meat could
not under any circumstance be defined to be "like" for
the purposes of Article III:4 of GATT. In addition, trenbolone,
zeranol and MGA were not naturally produced by animals. Thus,
meat from animals to which these hormones had been administered
contained residues of hormones which were not found in meat from
other animals, including animals treated for therapeutic purposes,
to which only natural hormones could be administered. In addition,
meat from animals treated with these hormones contained metabolites
from these hormones which did not appear in meat from other animals.
IV.340 The European Communities
further maintained that meat from animals to which any of the
three natural hormones had been administered for growth promotion
contained a level of residues which was in excess of the level
that it would otherwise contain. Moreover, as admitted by Canada,
the residues might be present in different proportions from those
found in nature, for example higher levels of male hormones in
female animals and vice-versa.254 Furthermore, meat from animals
treated with these hormones was more likely to contain an unusually
high level of residues than meat from untreated animals, in particular
where the hormones had been administered combined in "cocktails"
or in disregard of good animal husbandry practices. Obviously,
this risk was dominated or reduced when the hormones were administered
for therapeutic purposes under veterinary control.
IV.341 In addition, carcasses
from animals treated with hormones might differ in fat content,
fat composition, water content and connective tissue from those
of untreated animals. Combinations of androgens and oestrogens,
and androgens alone, decreased fat content and increased water
content, whereas combinations of progestagens and oestrogens increased
fat content, particularly in male animals. The use of trenbolone
and oestrogen decreased the amount of connective tissue and unsaturated
fatty acid in muscle. Cocktails of progestagens and oestrogens
altered the relative proportions of saturated and unsaturated
fat in treated carcases. In general, anabolic steroids had a
"partitioning" effect, resulting in the deposition in
carcasses of about 8 per cent more protein and 12 per
cent less fat.255
IV.342 The European Communities
argued that even if animals treated with hormones for growth promotion,
and meat thereof, and other animals, and meat thereof, were found
to be "like products", its measures would still be consistent
with Article III:4 because they afforded identical treatment
to imported products and to domestic like products. The European Communities
recalled that Canada had advanced two types of arguments in order
to justify its claim that beef from animals treated with any of
the sixth growth promoting hormones and other beef were "like":
(ii) that EC meat from untreated
animals contained residues of antimicrobial growth promoters and
other veterinary drugs.
IV.343 The European Communities
argued that the first of these two arguments was flawed. In the
first place, it did not account for the presence of residues of
the three synthetic hormones in meat from treated animals. These
residues were not found in meat from untreated animals and were
readily distinguishable from the residues of the three natural
hormones. Second, the fact that the residues from administered
hormones could not be easily distinguished from the residues of
those hormones naturally produced by animals did not mean that
there were no differences between the two types of meat. There
were substantial differences between them. The technical difficulties
to identify the origin of the residues had rendered it necessary
for the European Communities to require from importers a
certification that animals had not been treated, instead of conducting
inspection of meat at its borders, but it did not make the two
types of meat "like".
IV.344 The second argument was
equally misguided. As the European Communities had demonstrated,
hormones and antimicrobial growth promoters and other veterinary
drugs were different substances and posed different risks to human
health. Consequently, meat which contained residues of antimicrobial
growth promoters and other veterinary drugs was not "like"
meat which contained residues of administered growth promoting
hormones.
IV.345 The European Communities
disagreed with the Canadian interpretation of Article III:4.
The wording of Article III:4 called for a comparison between
the treatment given to "the products of the territory
of any contracting party imported into the territory of any other
contracting party ..." and the treatment accorded to "like
products of national origin ...", and not between
the treatment given to "any imported product"
and the treatment accorded to "any domestic like product".
The ordinary meaning of Article III:4 did not require that
a comparison be made on an import-by-import basis, but a comparison
of the treatment given to all imported products as a whole vis-a-vis
all domestic like products as a whole. In the EC view, the object
and purpose of Article III had been made explicit in the
general principle set forth in the first paragraph of that Article,
which stated that internal taxes and regulations "should
not be applied to imported or domestic products so as to afford
protection to domestic production". Article III:4 gave effect
to this principle with respect to internal regulations, other
than tax regulations and mixing regulations, and should be interpreted
in conformity with it. Where an internal regulation laid down
different requirements for imported and domestic products, it
might be assumed that domestic production was "protected"
if any imported product received "less favourable treatment".256
IV.346 The European Communities
argued that the situation was different where, as in the present
case, the internal regulation did not distinguish between imported
and domestic products but between different types of like products,
irrespective of their origin. The mere fact that an internal
regulation accorded more favourable treatment to certain types
of like products vis-a-vis other types of like products did not
necessarily mean that domestic production of the like product
as whole was protected. For that, it would be necessary that
those types of like product which were accorded more favourable
treatment were inherently or at least predominantly domestic and/or
that the types which received less favourable treatment were inherently
or at least predominantly imported. This view was supported in
the panel report on "US - Measures affecting Alcoholic and
Malt Beverages", which stated that:
IV.347 Although in the EC view
the panel report on "US - Measures affecting Alcoholic and
Malt Beverages" erred by ascribing the analysis of the effects
of a measure to the determination whether two products were "like"
and not exclusively on the characteristics of the products, this
panel report confirmed that Article III:4 was not infringed
unless a regulatory distinction between like products had the
effect of protecting domestic production.
IV.348 With reference to the
EC argument that the perception of European consumers was a relevant
factor in determining the "likeness" of a product, Canada
submitted that this factor was irrelevant. The public authorities
of WTO Members had a responsibility to educate the public and
to make them aware of scientific facts. If the Panel were to
allow "public perception" to become a factor in a "like
product" determination, it would open the door to misapprehensions
concerning scientific facts becoming the basis of a justification
in the WTO for the adoption of discriminatory measures. Such
an interpretation would obviously remove any incentive whatsoever
for public authorities in the European Communities to make their
populations aware of the scientific facts in respect of the six
hormones at issue.
IV.349 Canada observed that the
1987 panel report in "Japan - Customs Duties, Taxes and Labelling
Practices on Imported Wines and Alcoholic Beverages"258 dealt
with the issue of the relevance of consumer preferences in a "like
product" determination for purposes of GATT Article III:2.
The 1987 finding, which was cited with approval by the recent
panel on the same subject matter259 was that "... the traditional
Japanese consumer habits with regard to shochu provided no reason
for not considering vodka to be a 'like' product. ... "
Thus, in the context of Article III:2, two panels had expressly
rejected the relevance of consumer perception in a "like
product" determination. Canada submitted that consumer
perception was equally irrelevant in the context of GATT Article III:4.
IV.350 Canada pointed out that
the issue of whether regulatory differentiation of "like
products" could be justified under Article III:4 was
discussed by the panel report on "United States - Standards
for Reformulated and Conventional Gasoline".260 Having found
that "chemically-identical imported and domestic gasoline
are like products under Article III:4",261 the panel had
to deal with the US argument "that the requirements of Article III:4
[were] met because imported gasoline [was] treated similarly to
gasoline from similarly situated domestic parties - domestic
refiners with limited 1990 operations and blenders".262 The
panel rejected this argument.263 According to Canada, although the
facts in this case were different, it was useful to quote the
Panel's caution in response to the US attempt to justify regulatory
differentiation:
Thus Canada submitted that regulatory
differentiation by the European Communities between beef from
cattle to which the six hormones at issue had been administered
for growth promoting purposes and other beef, i.e., like
products, placed the Canadian beef at issue at a competitive disadvantage
and as such was inconsistent with Article III:4. IV.351 In any event, even arguendo accepting the EC reliance on the panel report in "United States -Measures Affecting Alcoholic and Malt Beverages", Canada submitted that the panel report did not support the EC proposition. The European Communities ignored the following paragraph in the same report that directly contradicted their argument:
IV.352 Canada therefore submitted
that Canadian beef and EC beef were "like products"
within the meaning of GATT Article III:4 and the European
Communities could not, consistent with that provision, ban the
importation of Canadian beef produced with the six hormones at
issue.
IV.353 The European Communities
recalled its previous arguments on Article III and disagreed
with Canada's contention that meat treated with hormones and hormone-free
meat were like because they "contain comparable residues".
It ignored the potential hazards which these residues posed to
human and animal health. It was the position of the European Communities
that these two types of meat were not like because hormone-treated
meat might cause cancer. Indeed, meat containing residues of
exogenously administered hormones was not different from meat
infected with a disease. The 1987 panel report on "Japan
- Customs Duties, Taxes and Labelling Practices on Imported Wines
and Alcoholic Beverages" referred to "traditional Japanese
consumer habits". The wish of the EC consumers to eat hormone-free
meat was not a habit and was not traditional. It evolved from
a number of examples reported in the European Communities
and elsewhere (e.g. Puerto Rico and the United States) of
the hazards arising from the use of these hormones, which had
been scientifically documented.
(b) Article XI
IV.354 Canada claimed
that, in the alternative, the EC import prohibition infringed
GATT Article XI, but noted that this claim should only be
considered by the Panel if it decided that Article III of
GATT did not apply in this case. Article XI of GATT set
out the obligations of Members with respect to the general elimination
of quantitative restrictions. Article XI:2 provided for
limited exceptions to the general prohibition of Article XI:1,
none of which were applicable in this case. Thus the European Communities
were prohibited from banning the import of beef produced with
growth hormones and had infringed Article XI of the GATT.
IV.355 The European Communities
responded that the measures at issue were internal regulations
within the scope of Article III of GATT. Therefore, Article XI
of GATT did not apply.
(c) Article XX
IV.356 Canada claimed
that Article XX of the GATT did not justify the infringement
demonstrated above of Article III or Article XI.
IV.357 The European Communities
submitted that in case the Panel were to find that measures infringed
Article III:4, they satisfied the requirements of the SPS
Agreement and, consequently, must be presumed to be in accordance
with GATT, and in particular with the provisions of Article XX(b).
5. Nullification and impairment
IV.358 Canada claimed
that the inconsistency of the EC measures with the SPS Agreement
and the GATT, or in the alternative with the TBT Agreement, established
a prima facie case of nullification or impairment pursuant
to GATT Article XXIII:1(a) and Article 3.8 of the DSU.266
However, even if the Panel were to decide that the EC measures
were consistent with the WTO Agreement, the application of the
EC measures nullified or impaired benefits accruing to Canada
under the WTO Agreement, within the meaning of Article XXIII:1(b)
of the GATT 1994. Article XXIII:1(b) had been interpreted
in GATT 1947 practice to mean even if a measure was not inconsistent
with a provision of the GATT, it might be challenged as nullifying
or impairing benefits. Article 26(1) of the DSU made it
clear that complaints concerning non-violation nullification and
impairment could be made within the new framework of the WTO Agreement.
Traditionally, three conditions were required by GATT 1947
panels for determining whether a case of "non-violation"
nullification or impairment existed. These conditions were:
(ii) the subsequent introduction
of a government measure that upset the competitive relationship
between the bound product with regard to like or directly competitive
imported products; and
(iii) that the measure at issue
could not have been reasonably anticipated at the time of the
negotiation of the tariff concession.267
IV.359 In the present case, all
of the relevant tariff items were subject to tariff concessions
by the European Communities.268 These concessions included
Canadian access to a tariff rate quota of 11,500 tonnes,
with an in quota rate of 20 per cent, for high quality, fresh,
chilled or frozen beef allocated to Canada and the United States
(the "Hilton beef quota"). 269
IV.360 The Hilton beef quota
had originally been granted by the European Economic Community
during the Tokyo Round Multilateral Trade Negotiations (contained
in the European Economic Community schedule of concessions
annexed to the Geneva (1979) Protocol), prior to the events which
ultimately led to the EC hormone ban. The Hilton beef quota originally
was a 10,000 tonne levy free tariff quota.270 When the Hilton
beef quota was established, the European Community had adopted
regulations which excluded Canadian high quality beef from its
scope, which had led to the establishment of a panel at the request
of Canada. The panel had ruled in Canada's favour, and this report
had been adopted by the GATT Council in March 1981.271 The European
Community subsequently amended its regulations to allow Canadian
high quality beef access under the Hilton beef quota. As a result
of the Uruguay Round Trade Negotiations, the European Communities
converted the Hilton beef quota to the tariff rate quota as indicated
above. Subsequently, in the Article XXIV negotiations of
1995, due to the accession of Finland, Sweden and Austria to the
European Communities, the European Communities increased the Hilton
beef quota to 11,500 tonnes.272
IV.361 Thus, the first requirement
of the traditional analysis of GATT 1947 panels had been met.
Second, the introduction of the EC measures had upset the competitive
relationship between Canadian and EC beef. Third, at the time
when Canada had won access to the Hilton beef quota, it could
not have reasonably foreseen the introduction of the EC measures.
Therefore, Canada claimed that benefits accruing to it under
the WTO Agreement had been nullified or impaired.
IV.362 The European Communities
responded that Canada failed to meet the minimum requirements
provided for in Article 26 of the DSU as regarded a detailed
justification of any non-violation complaints. In the present
case, Canada's claim of non-violation nullification and impairment
was unwarranted for the following reasons:
(ii) in any event, the measures
could have reasonably been anticipated by Canada at the time when,
according to Canada, the benefits accrued; and
(iii) Canada had not provided
any justification for its claim that the competitive relationship
between domestic and imported products had been upset by the adoption
of the measures. In fact, the consistency of the measures with
the WTO Agreements cited by Canada presupposed that the measures
were not capable of having such an effect.
IV.363 The European Communities
argued that the so-called "Hilton beef quota" granted
by the European Economic Community during the Tokyo Round
had been withdrawn during the Uruguay Round negotiations and replaced
by a new package of concessions on the same product. These new
concessions had become binding upon the European Communities
long after the introduction of the measures at issue. Thus, Canada
could not claim that these new concessions had been nullified
or impaired by the measures at issue.273
IV.364 During the Uruguay Round,
the European Communities had replaced this tariff quota by
an entirely new package of concessions, but it had done so in
the context of the new Agreement on Agriculture. Under the Agreement
on Agriculture, Members had agreed to achieve specific binding
commitments in the areas of market access, domestic support and
market competition. The concessions outlined below must therefore
be seen as new concessions negotiated in the context of a new
Agreement:
IV.365 This new package of concessions
on imports of beef was substantially different from, and more
"valuable" than, the Tokyo Round concessions on the
same product. It represented a new concession which had replaced
the Tokyo Round concession on the same product and was part of
a new "balance of concessions" achieved by the parties
during the Uruguay Round. The additional benefits obtained by
Canada must be regarded as the counterpart for Canada's own concessions,
including the renouncement by Canada to any outstanding nonviolation
rights with respect to the Tokyo Round tariff quota, which was
implicit in Canada's consent to the replacement of the old concession
by the new package of concessions.
IV.366 In the EC view, the present
case was to be distinguished from the case considered by the panel
on EC Oilseeds. In that case, the panel had found that
on the occasion of Article XXIV:6 negotiations following
the successive enlargements of the Community, the concessions
at issue had not been "modified" but rather "extended"
to the new EC member States. For this reason, the panel had concluded
that, despite the formal modification of the schedules of concessions,
the original "balance of concessions" had not been altered.
Hence the expectations created when the concessions had been
originally granted continued to be protected.274 However, the European
Communities argued that the present case differed from the EC Oilseeds
case in two fundamental respects. Firstly, in the present case
the Uruguay Round tariff concessions on beef were substantially
different from the preexisting concessions on the same product
since they were market access concessions as envisaged in Article 4
of the Agreement on Agriculture, a new Agreement. Secondly, the
new concessions on beef were granted as part of a negotiated exchange
of concessions; in the EC Oilseeds case, only
one party was required to make concessions. The findings of the
EC Oilseeds panel were therefore inapplicable
to the present case.
IV.367 The European Communities
argued that in any case, the measures at issue could have reasonably
been anticipated by Canada already at the time of the Tokyo Round.
Because there existed no international standards, guidelines
or recommendations on the use of hormones as growth promoters
in 1979, Canada could not reasonably assume that the European
Economic Community would not take any measures in order to restrict
their use to animals or meat from animals. Sanitary concerns
about the use of hormones as growth promoters predated the Tokyo
Round. When the Hilton beef quota had been negotiated, Canada
was aware that the safety of using hormones as growth promoters
was questioned in some scientific circles as well as by consumer
organizations and the general public. Canada was also aware that,
prompted by those concerns, a majority of EC member States, as
well as other countries, had already taken steps to restrict the
use of hormones.
IV.368 The European Communities
claimed that Canada had not advanced any justification whatsoever
for its claim that the EC measures had upset the competitive relationship
between domestic products and imports. In this regard, the Canadian
submission failed to meet the minimum requirements provided for
in Article 26 of the DSU. Unlike "violation" cases,
in "non-violation" cases there was no presumption of
"nullification and impairment". The burden of proving
that the measures at issue had in fact upset the competitive relationship
between domestic and imported products lay with Canada.
IV.369 Canada claimed
that the Hilton beef quota was not the subject of explicit negotiations
between Canada and the European Communities during the Uruguay
Round. In the agricultural area the Uruguay Round had made a
clear distinction between tariff rate quotas that confirmed pre-existing
access rights and new access rights.275 The current tariff rate
quota was listed in the Schedule of the European Communities under
the heading of "Current Access Quotas".276 Thus the Hilton
beef quota clearly fell within the category of quotas under which
existing market access opportunities were maintained. Canada
argued that even if scientific concerns could have been anticipated
in 1979, Canada could hardly have foreseen that the European Communities
would adopt the most trade-restrictive measures imaginable, i.e.,
a total ban on the importation of beef from cattle to which any
of the six hormones at issue had been administered for growth
promoting purposes. Furthermore, of the EC member States that
banned the use of growth promoting hormones before the EC ban
came into effect, at least one , Denmark, and possibly others
as well, did not prohibit the importation of beef produced with
the hormones at issue. Canada had submitted detailed information
on the devastating impact of the EC measures at issue on its beef
exports to the European Communities (paragraph 4.28).277
Therefore, Canada submitted that the European Communities had
nullified or impaired Canada's rights within the meaning of Article XXIII:1(b)
of the GATT.
IV.370 The European Communities
responded that Canada failed to meet the minimum requirements
provided for in Article 26 of the DSU as regards a detailed
justification in support of any nonviolation complaint.
No justification whatsoever was advanced for the claim that the
EC measures had upset the competitive relationship between domestic
production and imports. As for Canada's argument that the quota
of 11,500 tonnes allocated to the United States and Canada was
a current access quota and, hence, "falls under the category
of quotas under which existing market opportunities were maintained",
the European Communities noted that the term "current
access" was a term used during the Uruguay Round negotiations
for the purpose of drawing up market access commitments, in the
context of the Guidelines which had been developed for agriculture
negotiations. Such guidelines had become obsolete once the Uruguay
Round Schedules were finalized and the Final Act was signed.
In fact, the provisions of the Agreement on Agriculture contained
no reference to "current access" as a specific kind
of commitment, but only referred to "market access commitments"
(Article 4.1). The European Communities, therefore,
reiterated that the quota contained in the Uruguay Round Schedule
was part of a whole new balance of concessions, in the context
of a wholly new agreement, the Agreement on Agriculture. With
regard to the pretended nullification or impairment of benefits
accruing to Canada, the European Communities argued that
previous to the Uruguay Round, the only GATT commitment that the
European Communities had with respect to the tariff lines
concerned was the Tokyo Round commitments on high quality beef
tariff quotas, including the 10,000 quota to which Canada successively
gained access. No commitment existed for any beef outside of
high quality meat. Claims advanced by Canada concerning nullification
or impairment of benefits as regarded commitments on the tariff
lines mentioned above were, therefore, incorrect. At the time
of the negotiation of these concessions, the measures at issue
were already in existence. TO CONTINUE WITH EC MEASURES CONCERNING MEAT AND MEAT PRODUCTS (HORMONES) COMPLAINT BY CANADA
251 Panel report on "US - Restrictions on Imports of Tuna I", DS21/R (unadopted), 3 September 1991, 39S/155, 193-195, paras. 5.8-5.14. 252 Panel report on "EC - Animal Feed Proteins", para4.2. The other Panel report dealing with a regulatory measure discriminating between non-identical products is the Panel report on "US - Measures affecting Alcoholic and Malt Beverages". In this case, the panel found that low alcohol and high alcohol beer were "similar" in terms of physical characteristics but were not "like" for the purposes of Article III:4 because the distinction was not applied so as to afford protection to domestic production, BISD 39/206, pp.93-295, paras. 5.70-5.77. 253 Panel report on "Japan - Taxes on Alcoholic Beverages", para. 6.23. 254 The European Communities noted that, at para. 130 of its first submission to the Panel, Canada admitted that "for the purposes of growth promotion, animals are administered those hormones in which they are deficient. Generally, for growth promotion purposes, males are given oestrogens and gestagens, and females are given androgens". 255 1995 EC Scientific Conference Proceedings, pp.74-75 and 242. 256 Hence the "no-balancing" principle established by previous Panel reports which have dealt with formally discriminatory internal regulations. See panel report on "United States - Section 337 of the Tariff Act of 1930", adopted on 7 November 1989, 36S/345, 387, at para.5.14; and panel report on "US - Standards for Reformulated Gasoline", WT/DS2/R, paras. 6.14-6.15. 257 Panel report on "US - Measures affecting Alcoholic and Malt Beverages", para. 5.73 . 258 BISD 34S/83, para. 5.7. 259 "Japan - Taxes on Alcoholic Beverages", WT/DS8/R; WT/DS10/R; WT/DS11/R, para.6.23, footnote 103. 260 WT/DS2/R, 29 January 1996. 261 Ibid., para. 6.9. 262 Ibid., para. 6.11. The report explains further:
263 Ibid., see also paras. 6.13-6.16. 264 Ibid., para. 6.12. The panel report in "United States - Standards for Reformulated and Conventional Gasoline" was the subject of an appeal. The appeal, however, dealt only with issues related to Article XX and did not concern the Panel's conclusions regarding Article III:4. The report of the Appellate Body is contained in WT/DS2/AB/R, 29 April 1996. 265 Panel report on "US - Measures Affecting Alcoholic and Malt Beverages", BISD 39/206, para. 5.72. 266 Previous GATT 1947 panels had determined that a prima facie case of nullification and impairment is established where there is an infringement of obligations under the GATT. The DSU codifies this in Article 3.8 which provides that where obligations under an agreement such as the GATT or the TBT Agreement are infringed, the action is considered prima facie to constitute a case of nullification or impairment. 267 See "EC - Payments and Subsidies Paid to Processors and Producers of Oilseeds and Related Animal-Feed Proteins", report of the panel adopted on 25 January 1990, BISD 37S/86, paras. 142-154. 268 Uruguay Round Schedule LXXX - European Communities, Part I Most Favoured-Nation Tariff, Section I -Agricultural Products, Section I A Tariffs and Section I B Tariff Quotas, as subsequently modified. Tariff items covered by the EC beef and veal regime are:
269 Schedule CXL - European Communities, Part I Most-Favoured-Nation Tariff, Section I - Agricultural Products, Section I B Tariff Quotas. 270 "European Economic Community - Imports of Beef" from Canada, BISD 28S/92. 271 Ibid.. 272 Therefore, Canada maintained the increase in the Hilton beef quota did not amount to a rebalancing of concessions between Canada and the European Communities. See "EC - Payments and Subsidies Paid to Processors and Producers of Oilseeds and Related Animal-Feed Proteins", report of the panel adopted on 25 January 1990, BISD 37S/86, para. 145. 273 The European Communities explained that as regarded Canada, the concessions granted by the European Economic Community during the Tokyo Round negotiations with respect to imports of beef consisted of a 10,000 ton tariff quota for high quality beef with an in-quota rate of 20 per cent. In addition, imports within this quota were free from the variable levy applied at the time by the European Economic Community. No other tariff concessions had been granted by the European Economic Community with respect to imports of beef. Accordingly, imports of beef outside the quota were subject to customs duties and agricultural levies at the rate autonomously established by the European Economic Community. 274 Panel report on "EC - Payments and Subsidies Paid to Processors and Producers of Oilseeds and Related Animal Feed Proteins", adopted 25 January 1990, BISD 37S/86. 275 GATT Press Release NUR 080, 14 December 1993, on the Final Act of the Uruguay Round, p.9. 276 Schedule CXL of the European Communities (Schedule LXXX at the end of the Uruguay Round), Section I - B Tariff Quotas. 277 At the second meeting of the Parties with the panel, Canada produced a table which set forth eleven tariff lines of the European Communities (020610; 02061010; 02062210; 02062910; 02061091; 02062290; 02061099; 02062100; 02062999; 02109049; 16025090; 16029069) with regard to beef products which were bound prior to the Uruguay Round and the trade figures for each of these tariff lines from 1984 through 1995. |
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