OPINION OF ADVOCATE GENERAL
JÄÄSKINEN
delivered on 15 July 2010 (1)
Case C‑77/09
Gowan Comércio Internacional e Serviços Lda
v
Ministero della Salute
Reference for a preliminary ruling from the Tribunale amministrativo regionale del Lazio (Italy)
(Plant protection products – Active substance fenarimol – Directive 91/414/EEC – Inclusion in Annex I – Conditions and limitations – Directive 2006/134/EEC – Validity)
I – Introduction
1. In the present case the Tribunale amministrativo regionale del Lazio (Regional Administrative Court for Lazio, Italy) asks the Court to rule on the validity of Directive 2006/134/EC. (2)
2. Directive 2006/134 amended Directive 91/414/EEC, (3) which requires the Member States to ensure that plant protection products (in particular, herbicides, pesticides and fungicides intended for the treatment of plants) are not placed on the market and used in their territory unless they have authorised the product in question in accordance with the provisions of that Directive. A plant protection product may be authorised only if its active substances are listed in Annex I to Directive 91/414.
3. Directive 2006/134 added fenarimol to Annex I to Directive 91/414, subject to certain conditions.
4. In essence, the referring court is uncertain as to whether the validity of Directive 2006/134 may be affected by any difference between the Directive and a preparatory document relating to it, in the present case a report drawn up by the Member State which was designated to assess the effects of the active substance in question.
II – The legal context
A – Directive 91/414
5. Directive 91/414 lays down the Community scheme for the authorisation and withdrawal of authorisation to place plant protection products on the market.
6. Article 4 of Directive 91/414 provides that ‘Member States shall ensure that a plant protection product is not authorised unless … its active substances are listed in Annex I’.
7. Article 5(1) and (2) of Directive 91/414 lays down the conditions for the inclusion of an active substance in Annex I in the following terms:
‘1. In the light of current scientific and technical knowledge, an active substance shall be included in Annex I for an initial period not exceeding 10 years, if it may be expected that plant protection products containing the active substance will fulfil the following conditions:
(a) their residues, consequent on application consistent with good plant protection practice, do not have any harmful effects on human or animal health or on groundwater or any unacceptable influence on the environment, and the said residues, in so far as they are of toxicological or environmental significance, can be measured by methods in general use;
(b) their use, consequent on application consistent with good plant protection practice, does not have any harmful effects on human or animal health or any unacceptable influence on the environment as provided for in Article 4(1)(b)(iv) and (v).
2. For inclusion of an active substance in Annex I, the following shall be taken into particular account:
(a) where relevant, an acceptable daily intake (ADI) for man;
(b) an acceptable operator exposure level if necessary;
(c) where relevant, an estimate of its fate and distribution in the environment as well as its impact on non-target species.’
8. Article 5(4) of Directive 91/414 provides:
‘Inclusion of an active substance in Annex I may be subject to requirements such as:
…
– restrictions arising from evaluation of the information referred to in Article 6, taking account of the agricultural, plant health and environmental (including climatic) conditions in question,
…
– manner of use.’
9. Article 6 of Directive 91/414 is worded as follows:
‘1. Inclusion of an active substance in Annex I shall be decided in accordance with the procedure laid down in Article 19.
...’
10. Article 8 of Directive 91/414 relates to transitional measures and derogations. The second and fourth subparagraphs of paragraph 2 provide as follows:
‘After the adoption of this Directive, the Commission shall commence a programme of work for the gradual examination of these active substances … . This programme may require interested parties to submit all requisite data to the Commission and the Member States within a period provided for in the programme. A Regulation, adopted according to the procedure laid down in Article 19, will set out all the provisions necessary for the implementation of the programme.
…
… it may, following examination by the Committee referred to in Article 19 of such active substance, be decided by the procedure laid down in that Article that the substance can be included in Annex I and under which conditions, or, in cases where the requirements of Article 5 are not satisfied or the requisite information and data have not been submitted within the prescribed period, that such active substance will not be included in Annex I. The Member States shall ensure that the relevant authorisations are granted, withdrawn or varied, as appropriate, within a prescribed period.’
11. Article 19 of Directive 91/414 (4) provides that the Commission is to be assisted by a regulatory committee, the Standing Committee on the Food Chain and Animal Health (‘the Committee’).
B – Regulation (EEC) No 3600/92
12. The procedure to be followed under Article 8(2) of Directive 91/414 for the inclusion in Annex I to Directive 91/414 of certain active substances contained in plant protection products, is laid down by Regulation (EEC) No 3600/92. (5) The procedure begins with notification to the Commission which the producer must give pursuant to Article 4 of that Regulation.
13. It is clear from the preamble to Regulation No 3600/92 that the work of assessing active substances must be distributed among the competent authorities of the Member State and that a rapporteur Member State must be designated for each active substance.
14. In the present case, the producer of fenarimol, DowElanco Europe, notified the Commission, following which the latter adopted Regulation (EC) No 933/1994, pursuant to Article 5(2) of Regulation No 3600/92. (6) It appears from Regulation No 933/1994 that the Member State which was designated as rapporteur Member State is the United Kingdom of Great Britain and Northern Ireland.
15. Article 7 of Regulation No 3600/92 sets out in detail the obligations of the rapporteur Member State and the Commission respectively and the procedure to be followed. The rapporteur Member State must send the Commission a report on its assessment and a recommendation (paragraph 1). The Commission, for its part, must refer the dossier and the report to the committee for examination (paragraph 3) and then, where appropriate, submit a draft directive or a draft decision to the committee (second subparagraph of paragraph 3).
16. Furthermore, if additional trials or additional information are required, Article 8 of Regulation No 3600/92 lays down the obligations of the rapporteur Member State and the Commission respectively and the procedure to be followed.
C – Directive 2006/134
17. Directive 2006/134 included fenarimol in Annex I to Directive 91/414 for the period from 1 January 2007 to 30 June 2008 and laid down the restrictions on the use of that active substance. (7)
18. Recitals 2 to 8 of the preamble to Directive 2006/134 summarise the circumstances leading to its adoption and state the reasons for certain key decisions made by the Directive, particularly with regard to the restrictions on permitted uses (recitals 5 and 6), reduction of the period of inclusion (recital 8) and the need to obtain additional information (recital 10).
19. With regard to fenarimol, the Annex to Directive 2006/134 provides that its use as a fungicide is authorised only on certain crops (tomatoes, peppers in greenhouses, aubergines, cucumbers in greenhouses, melons, ornamentals, nursery trees and perennial plants). The annex also specifies the maximum rates for each crop. In addition, the annex prohibits certain uses of fenarimol (air application, knapsack and hand-held applications by amateur users, home gardening). Finally, the Member States must ensure that all appropriate measures are taken to mitigate risks and that particular attention is paid to the protection of aquatic organisms, earthworms, birds and mammals and to the protection of operators and workers.
III – The main proceedings and the question referred
20. On 28 July 1993 DowElanco Europe notified the Commission of its interest in having fenarimol included in Annex I to Directive 91/414. After taking over the business of DowElanco Europe, the Portuguese-law company Gowan Comércio International e Serviços Lda (‘Gowan’) continued the procedure for the inclusion of fenarimol in its own name.
21. Following the adoption of Directive 2006/134, Italy withdrew, by ministerial decision of 8 June 2007, the authorisations issued to Gowan for marketing plant protection products containing fenarimol.
22. By ministerial decision of 17 October 2007, fenarimol was placed on the list of active substances authorised in Italy, shown in Annex I to legislative decree no 194 of 17 March 1995.
23. The referring court observes that the decision of 8 June 2007 was partly revoked by a decision, the date of which is not given, in order to reinstate provisionally certain fenarimol-based products among those authorised in Italy, in accordance with legislative decree no 194, as amended on 17 October 2007 in the light of Directive 2006/134.
24. Gowan challenged the last two decisions by bringing an action for annulment before the Tribunale amministrativo regionale del Lazio.
25. In that action, Gowan claims that Directive 2006/134 was unlawful. In essence, it submits that the severe restrictions on the use of fenarimol are not justified by the scientific studies carried out in the course of the assessment procedure.
26. According to Gowan, the conditions for the inclusion of fenarimol in Annex I to Directive 91/414 restrict its use for a period of 18 months to certain crops of marginal importance by comparison with those which have hitherto constituted its main market (vines, apples, pears, peaches, water melons, courgettes, non-greenhouse peppers and strawberries).
27. The referring court finds that the scientific assessment procedure led to positive conclusions and that the Commission originally proposed to include fenarimol in Annex I of Directive 91/414 without any restriction.
28. As the Tribunale amministrativo regionale del Lazio was uncertain as to whether Directive 2006/134 is lawful, it decided to stay the proceedings and to refer the following question to the Court for a preliminary ruling:
‘In view of the fact that the conclusion of the technical and scientific assessment carried out by the rapporteur State appears to be that the risk arising from the use of fenarimol is acceptable, is Directive 2006/134, which significantly limited such use, valid?’
IV – Summary of the parties’ observations
29. Written observations have been lodged by the applicant in the main proceedings, the German and Greek Governments and the Commission. All, with the exception of the German Government, were represented at the hearing of 29 April 2010.
30. With the exception of the applicant in the main proceedings, all the parties represented took the view that Directive 2006/134 is valid.
V – Admissibility
31. The German Government and the Commission expressed doubts concerning the admissibility of the reference for a preliminary ruling on the ground that it is imprecise and unclear.
32. On that point, it has consistently been held that the need to provide an interpretation of Community law which will be of use to the national court makes it necessary that the national court should define the factual and legislative context of the questions which it is asking or, at the very least, explain the factual circumstances on which those questions are based. (8)
33. The information provided in orders for reference must not only enable the Court to reply usefully but must also give the governments of the Member States and other interested parties the opportunity to submit observations pursuant to Article 23 of the Statute of the Court of Justice. It is the Court’s duty to ensure that that opportunity is safeguarded, bearing in mind that under that provision only the orders for reference are notified to the interested parties. (9)
34. In the present case, the order for reference contains sufficient detail to enable the governments of the Member States and the other parties to submit observations. It is also clear from the observations submitted by the German and Greek Governments, and by the Commission, that those Governments and the Commission have been able to make a useful contribution on the question put by the referring court.
35. For my part, it seems to me that the Court may consider that it has sufficient information in the order for reference and in the observations which have been submitted to enable the Court to give a useful reply to the question before it.
36. However, there is another question relating to the admissibility of the present reference for a preliminary ruling which should be examined. That question is whether Gowan is still entitled to claim before the national courts that Directive 2006/134 is unlawful in view of the fact that Gowan did not bring an action for the annulment of the Directive before the Court of First Instance within the time lime prescribed in Article 230 EC, when it may still have had the right to do so. (10)
37. According to the judgment in TWD Textilwerke Deggendorf, a natural or legal person cannot, in principle, bring an indirect challenge to the validity of an act of a Community institution by means of a reference for a preliminary ruling if that person would have been entitled to do so directly on the basis of Article 230 EC. (11)
38. The limitation of the right to challenge a Community act by means of a reference for a preliminary ruling is intended to safeguard legal certainty by preventing Community measures which involve legal effects from being called into question indefinitely. Otherwise any person would be able to overcome the definitive nature which the decision assumes once the time limit for bringing an action under the fourth paragraph of Article 230 EC has expired. (12)
39. However, it is clear from the settled case-law that a person can be prevented from claiming before a national court that a Community measure is illegal and challenging its validity indirectly on the basis of Article 234 EC only if his right to bring an action for annulment under Article 230 EC is undoubtedly admissible. (13)
40. Consequently, as the question referred relates to a directive, it is necessary to ascertain whether an action brought by Gowan against Directive 2006/134 would undoubtedly have been admissible on the ground that its provisions concerned Gowan directly and individually. (14)
41. In my opinion, that is not the case here.
42. First of all, it must be observed that, in the TWD Textilwerke Deggendorf case, the undertaking in question was the subject of compliance measures. That case-law was applied to certain regulations when the Court stated that, in certain circumstances, a regulation could be a challengeable act, with the result that a reference for a preliminary ruling could be inadmissible. (15)
43. However, the situation is different with regard to directives. In the Eurotunnel case the Court made it clear that a directive could not be treated in the same way. (16)
44. Although it is true that, in the specific context of Directive 91/414, the Court of First Instance recently found that an action for annulment brought by a notifying undertaking against a directive adopted on the basis of that notification was admissible, (17) that does not mean that the applicant in the main proceedings in the present case undoubtedly has standing to bring such an action, and there are three series of reasons for this. First, the abovementioned judgment was given only in 2009, but the applicant in the main proceedings ought to have brought its action at the beginning of 2007, that is to say, long before the judgment was delivered. In addition, the Court of Justice has not had an opportunity to give a ruling on the General Court’s decision. Finally, taking account of the wording of the Treaty and its general system, which make no provision, even indirectly, for the possibility of such an action, I think the principle of legal certainty precludes such a restriction of admissibility by judge-made law. Therefore Gowan would not undoubtedly have had standing to bring an action against Directive 2006/134.
45. It follows that the question referred seems to me admissible.
VI – Analysis of the merits
A – Interpretation of the question referred
46. In the question referred, the referring court states that Directive 2006/134 significantly limited the use of fenarimol. The referring court wishes to know whether the Directive is valid, taking account of the fact that the technical and scientific assessment carried out by the rapporteur Member State appears to find that the risk arising from the use of fenarimol is acceptable.
47. First of all, I note that the question, which concerns the validity of a Community measure, is worded in a rather general way, without specifying the rule of law or the legal principle which may have been infringed.
48. In references for a preliminary ruling concerning validity, the questions and possible grounds of invalidity are often worded in a rather precise way by the referring court in the question itself. (18) Where that has not been the case, it has nevertheless been possible to clarify the question in the light of the order for reference itself. (19)
49. However, that is not the case here. The referring court has decided to put the question in rather general terms. To clarify the question, it might be possible to seek clues in the reasoning of the order for reference itself, but that is hardly more specific.
50. I would point out that Article 234 EC establishes the framework for close cooperation between the national courts and the Court of Justice, based on the division of jurisdiction between them. In the framework of that cooperation, the right to determine the questions to be submitted to the Court of Justice devolves upon the national courts alone and it is not for the parties to the proceedings before the Court of Justice to limit or extend the questions.
51. With regard to assessing the validity of an act, the situation is to a certain degree parallel with an action for annulment. As the Court has observed, requests for preliminary rulings on validity, like actions for annulment, constitute means for reviewing the legality of acts of the community institutions. (20) An action for annulment which does not indicate exactly the reasons why the contested act should be annulled is inadmissible. In the same way, a reference for a preliminary ruling concerning validity must be ruled inadmissible if the grounds of invalidity do not appear from the question or, alternatively, the decision. It is not for the Court to ascertain of its own motion any reason which could affect the validity of an act. (21)
52. With regard to the question concerning the validity of an act and the possibility of rewording the question, the Court should, in my opinion, abide by the question and refrain from expanding it. There are two sets of arguments in favour of that approach.
53. First, in an action for annulment it is for the applicant itself to choose and to formulate its complaints in its own way. A reference for a preliminary ruling, on the other hand, is a form of cooperation between the national court and the Court of Justice, and the parties to the main proceedings do not determine the procedure. The decision to refer a question is a matter for the national court alone. That court must also formulate the question and it is not for the Court of Justice, save in exceptional cases, to consider whether the decision is well-founded or to reword it, having regard to the rules of cooperation. With all the more reason it is not for the parties to expand the question formulated by the referring court.
54. Second, the preliminary ruling procedure is of the nature of an interlocutory matter in relation to the main proceedings, where the parties are able to argue in accordance with the principle that both parties should have the opportunity to state their case. In addition, unlike an action for annulment before the General Court, where two successive exchanges of pleadings are provided for (application and defence, then reply and rejoinder), a reference for a preliminary ruling from the Court of Justice is limited to a single statement of case by each party, lodged simultaneously, and the parties cannot submit written observations on the statements of the others. Furthermore, a hearing in an action for annulment is almost automatic before the General Court, but it is not for a reference for a preliminary ruling from the Court of Justice. (22)
55. In those circumstances, it is clear that the wording of the order for reference itself remains the keystone of cooperation. It is the document on the basis of which, first, the Member States decide whether or not to submit written observations and, second, each party to the procedure before the Court of Justice prepares its submissions. If it were generally accepted that the parties presenting written observations could take control of the procedure and thereby reword the questions referred to the Court in order to put forward other grounds of invalidity, that would open the way to changing the nature of the reference for a preliminary ruling into a covert action for annulment, at the risk of seriously disrupting the procedure before the Court. (23)
56. In view of those considerations, it is necessary to concentrate on the two factors giving rise to the doubts concerning the validity of Directive 2006/134 mentioned by the referring court in the order for reference, namely, first, the question of the relation between the report of the rapporteur Member State and Directive 2006/134 and, second, the fact that that directive makes the use of fenarimol subject to various conditions.
B – The relation between the report of the rapporteur Member State and Directive 2006/134
57. The referring court indicates that the fact that the report of the rapporteur Member State may not be consistent with the directive adopted may be a ground of invalidity.
58. In that connection it must be observed that it is clear from Regulation No 3600/92, and in particular Articles 7 and 8, that the adoption of any act by the Commission following an assessment (or by the Council, as the case may be) is preceded by a series of exchanges between different agencies.
59. With regard to the role of the rapporteur Member State in the present case, the applicant in the main proceedings and the Commission produced, on request by the Court, the report of the rapporteur Member State of March 1996, together with three addenda to the report dated August 2000, February 2001 and October 2003 respectively.
60. The Commission points out that, in that first report, it was not proposed to include fenarimol in Annex I to Directive 91/414, but to defer a decision as certain data were not available concerning its residues and its ecotoxic valency, that is to say, the risks to aquatic organisms.
61. The Commission also claims that the reports were submitted for evaluation by the other Member States. In the course of that examination by national experts, which took place between 1997 and 2004, the other Member States proposed modifications and additions to the reports.
62. According to the Commission, from November 2000 the report was discussed by two working groups. The ‘evaluation’ working group examined the substance of the report from a technical and scientific viewpoint with the object, in particular, of determining the level of risk on the basis of scientific data (risk assessment). The ‘legislation’ working group is responsible for preparing the draft directive on inclusion, taking account, where necessary, of a broader assessment of risk management in the event of scientific uncertainty. The ‘legislation’ working group must take into account political and social considerations. It establishes the level of scientific uncertainty acceptable to society and evaluates the possibility of managing and containing the risk which has been recognised (risk management).
63. In the present case, the activities of the working groups continued from 2000 to 2004 in relation to the technical and scientific assessment alone. Even before they began, a number of Member States had presented contributions in the form of addenda in the course of the joint assessment.
64. According to the Commission, the first version of the draft directive was not presented until 2004. However, between 27 July 2004 and 13 September 2006 the Commission prepared no less than eight different versions of the directive, three of which were discussed by the ‘legislation’ working group and one was submitted for a vote by the committee.
65. The applicant in the main proceedings and the Commission have presented somewhat differing accounts of the process of adoption of the directive in question. Accordingly the Court has three different versions of events – those of Gowan and the Commission, and the version in the preamble to the directive. In the context of a reference for a preliminary ruling, it is certainly not necessary to examine those different versions in detail. (24)
66. So far as the question referred is concerned, the national court does not make it clear how the alleged difference between the report and the directive may affect the validity of the latter. Furthermore, the national court does not specify to which of the three reports it is referring.
67. On that point, it must be observed that a direct correlation between a report prepared by the rapporteur Member State and the act adopted by the Commission cannot be established.
68. The report of the rapporteur Member State and the addenda are used as the starting point for discussions with the Member States’ experts and when the inclusion of active substances is considered by the ‘evaluation’ and ‘legislation’ working groups. The first draft of a directive is drawn up by the Commission only on completion of that complex process.
69. By virtue of a fundamental rule of the Treaty, the Commission may at any time modify its draft or replace it with a new draft taking account of comments, as was the case here. With regard to legislative proposals, Article 293(2) TFEU expresses that rule.
70. In the process of adopting any directive pursuant to Directive 91/414, the Commission has a discretion in at least two respects, that is to say, it assesses the risks and carries out a political evaluation of their acceptability.
71. Risk assessment is a fairly objective exercise provided that an established and undisputed methodology exists, but where there is none (as in the present case for fenarimol) opinions are necessarily expressed in the exercise of a discretion. (25) An assessment of the risks revealed by analysis necessarily entails choices of a political and social nature which are for the Commission to make.
72. In any case, this is a field characterised by complex evaluations and a broad discretion. It is a field in which the Court should censure decisions only in the event of a manifest error of fact or of law or a misuse of power. As the General Court has observed, if the Commission is to be able to pursue effectively the objective assigned to it, account being taken of the complex technical assessments which it must undertake, it must be recognised as enjoying a broad discretion. (26)
73. In the present case, it is not possible to go into detail in view of the brevity of the question referred on that point. Furthermore, there are differences in the accounts of the facts given by the applicant in the main proceedings and the Commission with regard to the stages which preceded the adoption of the Directive. The very nature of the preliminary ruling procedure before the Court does not seem to me to permit the clarification of factual questions of that kind. In those circumstances, no more can be said.
74. The conclusion that must be drawn from the foregoing is that any document drawn up by the rapporteur Member State in connection with Regulation No 3600/92 is a document which is necessary and useful for the preparation of the Commission’s opinion, but it is not in itself decisive or determining. It is merely a preparatory document. The act in question could be rendered invalid only by flagrant inconsistency between, on the one hand, a report based on an undisputed methodology leaving no room for scientific uncertainty and, on the other hand, the Commission’s opinion.
75. However, the file does not reveal any such inconsistency which would be capable of calling into question the validity of Directive 2006/134.
C – Use of fenarimol subject to conditions laid down by Directive 2006/134
76. The referring court is doubtful as to the validity of Directive 2006/134 also on the ground that it significantly limited the use of fenarimol. However, the court does not specify which conditions in particular are likely to affect the validity of the Directive. Therefore my analysis will be in general terms.
77. It must be noted that, according to Article 5 of Directive 914/14, various conditions may be imposed when an active substance is included in Annex I of the Directive.
78. With regard to the conditions laid down by Directive 2006/134 for fenarimol, it must be borne in mind that the general principle of proportionality requires that measures adopted by Community institutions do not exceed the limits of what is appropriate and necessary in order to attain the legitimate objectives pursued by the legislation in question; when there is a choice between several appropriate measures, recourse must be had to the least onerous, and the disadvantages caused must not be disproportionate to the aims pursued. (27)
79. It follows from this that, within the context of judicial review of the application of such a principle, having regard to the broad discretion enjoyed by the Commission in adopting Directive 2006/134, the legality of that measure can be affected only if the measure is manifestly inappropriate having regard to the objective which the Commission sought to pursue. (28)
80. With regard to the statement of reasons of Directive 2006/134, reference must be made to the following matters set out in its preamble.
81. On the basis of the various examinations that were carried out, the Commission considers that plant protection products containing fenarimol may be expected to satisfy the requirements laid down in Article 5(1)(a) and (b) of Directive 91/414/EEC, with regard to the uses which were examined and detailed in the Commission review report, provided that adequate risk mitigation measures are applied. (29)
82. The Commission points out, however, that fenarimol is a hazardous substance. Therefore its use should not be authorised without restriction. The Commission refers to concerns about its intrinsic toxic effects, including potential endocrine disrupting properties and to the fact that there is at present no scientific consensus on the exact extent of the risk. Applying the precautionary principle, and taking into account the current state of scientific knowledge, the Commission decided to impose risk mitigation measures in order to achieve the high level of protection of human and animal health and the environment chosen in the European Community. (30)
83. For that purpose, inclusion in Annex I to Directive 91/414 is limited to the proposed uses of fenarimol that have been actually assessed within the Community evaluation and which were considered to comply with the conditions of Directive 91/414. Consequently other uses, which were not or only partially covered by this assessment, must first be subject to a complete assessment, before their inclusion in Annex I to Directive 91/414 can be considered. (31)
84. Furthermore, with regard to the period of inclusion, the Commission considers it appropriate to limit the period to 18 months. According to the Commission, this further reduces any risk by ensuring a priority re-assessment of the substance. (32)
85. It seems to me that these passages in the preamble to Directive 2006/134 prove that the Commission carried out an overall assessment of the advantages and disadvantages of the system to be put in place and that, in any case, the system was not manifestly inappropriate in the light of the objectives pursued.
86. In addition, the substantive conditions and the time restrictions imposed in relation to fenarimol do not seem at all exceptional by comparison with those adopted on the same day by different directives for certain other active substances such as methamidophos, procymidone, flusilazole, carbendazim and dinocap. (33)
87. Therefore the fact that Directive 2006/134 includes conditions such as those provided for in the present case in accordance with Article 5 of Directive 91/414 does not in itself affect its validity.
VII – Conclusion
88. I therefore propose that the Court give the following reply to the Tribunale amministrativo regionale del Lazio:
Examination of the question which has been referred reveals nothing which would justify the conclusion that Commission Directive 2006/134/EC of 11 December 2006, amending Council Directive 91/414/EEC to include fenarimol as active substance, was not validly adopted.