C-272/80
ECLI:EU:C:1981:312
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JUDGMENT OF 17. 12. 1981 — CASE 272/80
In Case 272/80
REFERENCE to the Court under Article 177 of the EEC Treaty by the Sixth Chamber of the Gerechtshof (Regional Court of Appeal), The Hague, for a preliminary ruling in the criminal proceedings pending before that court against
FRANS-NEDERLANDSE MAATSCHAPPIJ VOOR BIOLOGISCHE PRODUCTEN BV, whose registered office is at 54 Oudorpweg, Rotterdam,
on the interpretation of Article 30 of the EEC Treaty in the light of the Netherlands Law of 1962 relating to plant protection products,
T H E COURT
composed of: J. Mertens de Wilmars, President, G. Bosco, O. Due and A. Touffait (Presidents of Chambers), P. Pescatore, Lord Mackenzie Stuart, A. O'Keeffe, T. Koopmans, U. Everling, A. Chloros and F. Grévisse, Judges,
Advocate General: S. Rozès Registrar: A. Van Houtte
gives the following
JUDGMENT
Facts
The facts of the case, the procedure and Court], Rotterdam, the private limited the written observations may be company Frans-Nederlandse Maat- summarized as follows: schappij voor Biologische Producten BV was fined the sum of HFL 1 000 for an offence contrary to the Bestrijdings- I — Facts and procedure middelenwet [Law relating to plant protection products], 1962. During the 1. By judgment of 4 December 1979 of proceedings before the Arron- the Arrondissementsrechtbank [District dissementsrechtbank it was found that
FRANS-NEDERLANDSE MAATSCHAPPIJ VOOR BIOLOGISCHE PRODUCTEN
the défendant company had, on 16 time, it did not restrict trade to the least February 1978, through the intermediary extent possible. Moreover, the exam- of a representative, sold or delivered, or ination to which the product must be both, in the Netherlands, to the company subjected in the Netherlands for the Noord-Nederlandse Bottelmaatschappij purpose of obtaining approval involved BV, a certain quantity of a product costs which were completely dispro- called "Fumicot Fumispore", a plant portionate to the turnover which could protection product within the meaning of be achieved in the Netherlands. Article 1 of the above-mentioned Law, which is designed in particular for use in the food-processing industry but did not appear to have been approved in the Netherlands in accordance with the 3. The product in question Bestrijdingsmiddelenwet since its packaging did not indicate its name or its approval number. The product was used by the company Noord-Nederlandse Bottelmaatschappij BV to fumigate and It appears from the Plant Health Index disinfect a sugar silo so as to eliminate for Insecticides, Fungicides and any traces of mould. Herbicides . . . , laid down by the French Association for Technical and Agri- cultural Coordination, that it is a product under the name "Fumicot Auto- comburant Fumispore", marketed by LCB (Chemical and Biological 2. The defendant company lodged an Laboratory), La Salle, France. The appeal against that sentence, claiming product contains an active substance, in particular that the prohibition laid parahydroxyphenyl-salicylamide, and is down in Article 2 of the Bestrijdings- packed in a container comparable to a middelenwet restricting the importation soft-drinks carton. and marketing in the Netherlands of the product in question constituted a quantitative restriction or a measure having equivalent effect prohibited by Article 30 of the EEC Treaty. Counsel According to the Plant Health Index: for the company stated that the product in question was imported from France where it was lawfully marketed after it had been approved in accordance with "This substance, better known in phar- the relevant French legislation which macology under the name of 'Driol', sought to protect exactly the same exists in the form of a fine powder, not interests, namely those of public health, readily soluble in water, purplish grey as the Netherlands legislation, and to the and with a faintly acrid smell. It has been like extent. In those conditions, a found to have fungicidal properties in requirement that the product in question regard to numerous fungi or moulds in should, on importation into the storage premises (Pénicillium, Netherlands, be the subject of a fresh Cladosporium, Altenaria, Rhizopus . . . ) . approval was not necessary in order to When used it is mixed with a smoke- satisfy an overriding requirement nor did Droducer which disperses and suspends it it justify an exception to the fundamental at a rate of concentration of 5%. right of the free movement of goods. Application: disinfection of premises used Nor, furthermore, did it constitute the f or the manufacture and storage of food most suitable means since, at the same products (0.15g/m 3)."
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This product is used mainly in the food The details of the approval procedure industry in bakeries, premises used for are laid down in the above-mentioned cheese-making and dairies. decree. Approval is granted for a maximum period of 10 years and may be made subject to conditions relating to In France, it was the subject of sales use and safety. Finally, there is a approval No 74 00 949, the grant of procedure by which an appeal may be which was most recently extended by brought against a decision to refuse or approval dated 17 July 1980. On the withdraw the approval. other hand, no approval of the product has been issued in the Netherlands. A request to that effect was, however, On the other hand, the competent auth- made on 3 May 1967. orities are under no duty to have regard to analyses, examinations and tests carried out in other Member States where the product is approved. 4. The relevant national laws
5. In France, Law No 525 of In the Netherlands the importation and 2 November 1943 relating to the organ- marketing of plant protection products ization and control of anti-parasitic such as the product in question are products for agricultural use (in the governed by the Bestrijdingsmiddelenwet version now in force) prohibits the and by its implementing decrees. Article importation, sale, marketing or distri- 2 (1) of that Law provides: bution (even free), of such products, which doubtless include Fumicot Fumispore, without prior approval "It shall be an offence to sell, to store or (Articles 1 and 1 bis). Approval is to use a plant protection product where granted once it has been established that it is not shown that the said product has the products are effective and harmless been approved pursuant to this Law." to public health, users and plants and animals. Products in respect of which a request for approval is made must Approval is granted by a decision of the undergo physical, chemical or biological Minister for Agriculture and Fisheries or tests in the laboratories and departments by the Minister for Public Health and of the Ministry of Industrial and Environmental Hygiene, once it has been Scientific Development and decisions are established that the product is fit for the taken by the Minister for Agriculture use for which it is intended, does not and Rural Development, acting on a give rise to any harmful effect and that proposal from an approvals committee its content of active substances does not (Article 3). exceed that necessary for the purpose which it is designed to achieve (Article 3). Applications for approval are Provisional sales approvals of four years' addressed to the Plant Protection duration may, also be granted and the Products Approvals Committee and approvals (which are renewable) are involve the payment of a fixed amount granted for a maximum period of 10 for their examination (Article 4 of the years. There is a right of appeal for Decree relating to the approval of Plant aggrieved parties. The packaging or Protection Products of 28 November labelling of products which have been 1980). approved must clearly state the
FRANS-NEDERLANDSE MAATSCHAPPIJ VOOR BIOLOGISCHE PRODUCTEN
composition and name of the product Adviser at the Ministry of Foreign and the fact that it has been approved, as Affairs; on 23 March 1981 by the well as precautionary measures and Government of the Italian Republic, counter-indications. represented by Arnaldo Squillante, Head of the Department of Diplomatic Legal As the Commission states in its replies to Affairs, Treaties and Legislative Matters, the Court dated 12 June 1981, the and by Pier Giorgio Ferri, State French legislation is comparable to and Advocate; on the same date by the seeks to protect the same interests of United Kingdom, represented by Mrs G. public health as the Netherlands Dagtoglou, Treasury Solicitor's Depart- legislation with certain minimal ment. differences.
6. By judgment of 29 October 1980, 8. Upon hearing the report of the registered at the Court on 10 December Judge-Rapporteur and the views of the 1980, the Gerechtshof [Regional Court Advocate General, the Court decided to of Appeal], The Hague, referred the open the oral procedure and to invite the following question to the Court: Commission to reply in writing to certain questions before the hearing. "Is the scheme of the Netherlands Law of 1962 relating to plant protection products compatible with Article 30 of the EEC Treaty in so far as that Law prohibits the marketing in the II — Written observations sub- Netherlands of a product originating in mitted to the Court pur- another Member State in which that suant to Article 20 of the product has been lawfully marketed and Protocol on the Statute of in which it meets the legislative the Court of Justice of the requirements which protect the same EEC overriding requirements of public health as the Netherlands Law?" 1. Observations of the appellant in the 7. In accordance with Article 20 of the main proceedings Protocol in the Statute of the Court of Justice of the EEC, written observations were submitted on 19 February 1981 by The appellant in the main proceedings the Commission of the European states that the system of the Netherlands Communities, represented by its Legal Law relating to plant protection products Adviser, Rolf Wägenbaur, acting as constitutes, in respect of all those Agent, assisted by Thomas Van Rijn, a products intended to be used on the member of its Legal Department; on 6 Netherlands market, an identical March 1981 by the appellant in the main obstacle to their approval. The Law proceedings, the company Frans-Neder- makes no reference to Community law landse Maatschappij voor Biologische and, for the purposes of its application, it Producten BV, represented by W. L. is of no consequence that a product orig- Nouwen; on 13 March 1981 by the inating in another Member State has Netherlands Government, represented by been lawfully marketed there and that it M. F. Italianer, Secretary-General of the also satisfies in that country legislation Ministry of Foreign Affairs; on 19 designed to guarantee the same March 1981 by the Danish Government, requirements of protection of public represented by Laurids Mikaelsen, Legal health as the Netherlands Law.
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The appellant in the main proceedings "To the extent to which the Law of 1962 contends that the absence of harmon- relating to plant protection products ization within the Community, under duplicates, as regards its application and Article 100 of the Treaty, of the its objective, the French legislation to conditions governing the approval of which the product in question is subject, plant protection products does not justify the system established by the said Law is the existence of systems which are not binding under the law of the incompatible with Article 30 et seq.
It European Economic Community which states that that view is founded on is in force." reasoning a contrario which is based without qualification on the judgment in Case 148/78 Ratti [1979] ECR 1629, 2. Observations of the Commission and which, in view of the judgments of the Court of 20 February 1979 in Case 120/78 Rewe [1979] ECR 649 and of 26 The Commission states that, in all the June 1980 in Case 788/79 Gilli and Member States with the exception of Andres [1980] ECR 2071, is far too Ireland, the marketing of plant
broad. In its opinion those judgments protection products is subject to the only permit a derogation, by virtue of grant of prior approval, subject to sub- Article 36 of the EEC Treaty, from the stantive conditions which the prohibition laid down in Article 30 Commission considers to be comparable. where the subsisting obstacle to trade is It is generally required that the products strictly necessary to protect the interests should present no danger to the health enumerated in Article 36. of humans and animals or an unreasonable danger to the environment This restriction upon recourse to Article and that they should be effective (with 36 of the EEC Treaty also applies where the exception of Luxembourg and the the matter is not governed by a directive United Kingdom as regards the latter based on Article 100 of the Treaty. point). The administrative provisions for the implementation of national laws Since the product satisfies French vary, according to the Commission, to a legislation which protects the same large extent in their scope.
The requirements of public health, Article 36 Commission observes that the conditions may no longer be invoked in relation to laid down in these provisions are the application of Article 30 to the generally neither mandatory nor product in question. complete. In general, however, Member States have gradually made their national As to the extent to which relevant provisions conform to the recommen- legislation in the Member State where dations of the Council of Europe relating the product is first placed on the market to the detailed rules governing the also covers the overriding considerations approval and registration of plant mentioned in Article 36, the appellant in protection products.
But what is different the main proceedings argues that that is the application of those provisions question must be decided by the court of which varies according to agricultural or the Member State in which the product ecological conditions and the scientific is marketed again and where national evaluation of the information supplied. legislation imposes restrictions on the marketing of the product. So far as Community law is concerned, Therefore, the defendant company the Commission goes on to refer to its proposes that the following reply should proposal for a Council directive be given to the preliminary question: concerning the placing of EEC-accepted
FRANS-NEDERLANDSE MAATSCHAPPIJ VOOR BIOLOGISCHE PRODUCTEN
plant protection products on the market Member States to recognize or validate and the establishment, in collaboration approvals granted by other Member with experts from the Member States, in States even where, as in the present case, draft form of a number of uniform two Member States have rules inspired principles based to a large extent on the by the same concerns in regard to the recommendations of the Council of protection of public health. Europe.
The Commission proposes in its obser- The Commission maintains that its vations with regard to the meaning of viewpoint remains valid even in the light the preliminary question that the of the judgment of 16 December 1980 in question should be reformulated so as to Case 27/80 Fietje [1980] ECR 3839, place the problem of the interpretation of particularly since in the field of Article 30 of the EEC Treaty in the consumer information, which was at context of the facts of the case. issue in that case, it is possible to be more flexible than in questions of public The Commission considers moreover health. Not only the public, but also the that the problem falls to be examined in State which is responsible for ensuring the context of the implications of the the health of its citizens, must be certain decision of the Court in Case 120/78 that a plant protection product does not referred to above and of subsequent pose any threat to health. The decisions. The Commission states that, Commission's view is that there is according to well-etablished case-law, in undoubtedly a presumption to that effect the absence of common rules governing if the product is a product approved in the production and marketing of another Member State following a pesticides, it is for the Member States to procedure and as a result of examin- regulate within their respective territories ations which are probably, but may not all matters concerning the production always be, equivalent. But the and marketing of those products, even if Commission points out that a that amounts to a measure having an presumption does not amount to a effect equivalent to a quantitative certainty. Therefore the Commission restriction on imports within the meaning goes on to state that as long as the of Article 30 of the Treaty. The interpret- question of the recognition of approvals ation of the Court, in Cases 120/78 and (granted according to mutually agreed 788/79 mentioned above, according to criteria) has not been resolved at which products lawfully produced and Community level, there can be no marketed in another Member State must question of inferring that recognition be capable of being imported and from the application of Article 30. marketed freely in the other States is limited to Article 30 and thus leaves open, in the Commission's view, the possibility that national restrictions may If however there should be an inclination in exceptional cases be justified by one to make the answer depend upon or more of the considerations mentioned whether or not there are equivalent in Article 36 of the Treaty. conditions for the approval of plant protection products, the Commission points out that it must be borne in mind Moreover, the Commission acknow- that "it is for the national court to make ledges that the prohibition of the impor- the findings of fact" in that respect "in tation and marketing of plant protection order to establish whether or not there is products without prior approval by the such equivalence" ( j u d g m e n t in Case importing Member State is justified by 27/80 mentioned above, paragraph 2 of the absence of Community rules obliging the decision). The Commission states
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that if it is not thought sufficient to concerned with the placing on the verify the provisions laid down by laws market and the use of plant protection and regulations but that it is also products. The resulting obstacles to necessary to take into account examin- intra-Community trade are, in the view ations and analyses actually carried out of the Netherlands Government, in respect of each product, the national necessary by reason of the overriding court might easily find that task beyond requirements relating inter alia to the it, in view of the complexity of the protection of health and life of humans matter. and animals, the preservation of plant life, or the protection of the
The Commission concludes by stating environment, and must be validated that the solution which it proposes may under Article 36 of the Treaty provided be inferred from the judgment recently such national measures are justified and delivered by the Court in Case 53/80 do not give rise to unreasonable (judgment of 5 February 1981, Officier consequences. van Justitie v Koninklijke Kaasfabrìek Eyssen BV[1981] ECR 409). The Netherlands Government considers that a national control is wholly justified In the result, the Commission proposes in order to enable a Member State to that the following reply should be given adopt provisions which are more precise to the preliminary question: and better suited to the climatic and "Articles 30 and 36 of the EEC Treaty geographical conditions which differ are to be understood as meaning that fundamentally from one country to rules of a Member State prohibiting, in another.
This cannot be guaranteed by the absence of the approval required in the original approval alone. the interests of public health, the marketing of a product originating in The Netherlands Government adds that another Member State do not come the fact that a proposal for a Council within the prohibition of measures directive concerning the placing of EEC- having an effect equivalent to accepted plant protection products on quantitative restrictions even if that the market (Official Journal 1976, C product is lawfully marketed in the 212, p. 3), which was submitted by the Member State of origin and has there Commission to the Council on 4 August obtained the required approval." 1976, has not yet been adopted, is an indication that the Member States consider that the conditions governing
3. Observations of the Netherlands the use of plant protection products Government inevitably vary too widely from one State to another. The Netherlands Government underlines the need to adopt legislative measures to As regards the inspection and analysis of ensure the mandatory protection of the those products, operations which it human, animal and plant environment considers necessary, the Netherlands against the harmful effects of plant Government observes that a Member protection products. State must have at its disposal the The Netherlands Government does not relevant information which, however, is in any way deny that a national system not available when a plant protection of approval for plant protection products product, which has been approved in does indirectly impede the importation of another Member State, may, without any those products but it considers that as further requirement, be sold in another long as no Community rules in the Member State.
The Netherlands matter have been adopted Member States Government also considers it worthwhile are free, as regards their own territory, to emphasize that any restrictions on use to adopt rules governing all matters which may have been imposed in the
FRANS-NEDERLANDSE MAATSCHAPPIJ VOOR BIOLOGISCHE PRODUCTEN
Member State which granted the original Denkavit [1979] ECR 3369 and its approval have no legal status in any judgment of 20 May 1976 in Case other Member State. 104/76 Centrafarm [1976] ECR The Netherlands Government finds that 613.); there is an analogy between the national (ii) obstacles may be tolerated to the systems of approval and registration for extent to which the national plant protection products and those provisions are indispensable from the governing medicinal preparations. In the point of view of the protection of case of medicinal preparations a system public health, the fairness of of approval and registration is generally commercial transactions and considered to be acceptable and just. The consumer protection, as is indicated Netherlands Government poses the by the judgments of the Court of 20 question whether such a system is not February 1979 in Case 120/78 Rewe even more necessary in the case of plant (mentioned above), of 26 June 1980 protection products and observes that in in Case 788/79 Gilli (mentioned fact all Member States have a national above), and of 19 February 1981 in
system of approval and registration. Case 130/80 Kelderman [1981] ECR The Netherlands Government concludes 527. that, in view of the problems in regard to the composition of those products, their The Danish Government, too, considers continuing development and their that pesticides may involve, by their very widespread use, and in the absence of nature, risks to plants, animals or man Community harmonization in this and, in the broad sense, to the sphere, a system of prior national environment. As the present case shows, approval in each Member State remains a such considerations and concerns are at flexible and effective system for the the basis of the legislative provisions protection of public health and can be adopted by the Member States.
It is thus applied in a way which does not give rise possible, according to the Danish to discrimination and does not Government, for national laws to pursue, unnecessarily impede trade between in the general interest, certain ends Member States. which may justify exceptions to the The Netherlands Government therefore general rules of the Treaty concerning proposes that the Netherlands legislation the free movement of goods. should be declared to be compatible with Article 30 et seq. of the EEC Treaty. The Danish Government considers that Member States must be free to lay down legislative provisions which are essential
4. Observations of the Danish for achieving the objective of the Government protection of public health. According to The Danish Government submits in the the Danish Government, it is therefore first place that it is clear from the not unreasonable to require that a case-law of the Court that: product which is intended to be used as a plant protection product and is approved (i) the prohibition laid down by Article for that purpose in another Member 30 of the EEC Treaty also extends, State, should also be made subject to by analogy with the solutions approval in conformity with the adopted by the Court with regard to legislation of the importing State. veterinary inspections, to systematic procedures for the approval of plant The Danish Government is of the protection products imported from opinion that the measures in question other Member States. (In this respect imposed by the Netherlands legislation it cites the judgment of the Court of cannot be considered as discriminatory 5 October 1977 in Case 5/77 in their effect or as having been inspired
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by considerations having no connection The rule of Community law in question with the aims of Article 36 of the Treaty. would thus be diverted far from its true purpose and would wrongly assume the The Danish Government proposes function of an instrument for promoting therefore that the Court should reply to the standardization of the national the question submitted to it by stating systems according to a reasoning and that "the application of national spirit completely alien to the Treaty. legislation relating to the use of plant protection products such as those The Italian Government observes that if mentioned in the judgment making the such an interpretation were accepted it reference to the Court, is not would follow that machinery other than incompatible with the rules of the EEC that provided for by the Treaty (Article Treaty relating to the free movement of 100) could be used to standardize goods and that that is also the case even national rules affecting free trade within if the product has been lawfully the common market. marketed in the Member State of origin The Italian Government does not and satisfies analogous legislative consider that the relevant provisions of requirements in that country". the Netherlands legislation constitute an impenetrable barrier to the placing on
5. Observations of the Government of the the market of foreign products or that Italian Republic they may be equated with a restriction on imports within the meaning of Article The Italian Government considers that 30 of the Treaty, particularly since they the problems raised by this case concern do not discriminate between national and the application of Article 36 of the foreign products. Treaty. It maintains that Article 36 confers upon the Member States a power If, on the other hand, the imported in regard to the protection of the product were exempted from the interests mentioned in that article, even if obligations imposed by the national that involves having recourse to means public health legislation which continues which constitute a hindrance to intra- to apply to national products, the Italian Community trade, provided that such Government's view is that the opposite means are necessary for the purposes of effect would be achieved, namely that of
protection. In exercising that prerogative creating a privilege and consequently, an each Member State may act with unjustified disturbance of the equilibrium complete independence and may of the market. consider, according to the case, that a As a result, the Italian Government product is dangerous to health or, on the proposes that the Court should give the contrary, harmless and therefore following reply to the question raised by exempted from any restriction. the Netherlands court: In the view of the Italian Government, it "(a) A Member State is empowered to is inconceivable that the exercise by one prohibit, by means of its own rules, Member State of an option open to it the placing on the market of a could bind other Member States of the product considered as dangerous to
Community. If that were in fact the case public health, even if that the other States would be deprived of the prohibition affects an imported power which is conferred upon them by product approved under the public Article 36 and would be required to align health legislation of the country of their public health legislation with the origin; legislation of the State which had adopted the most liberal provisions on (b) The existence of a national rule of this point. law laying down, for a series of
FRANS-NEDERLANDSE MAATSCHAPPIJ VOOR BIOLOGISCHE PRODUCTEN
products, including plant protection In the view of the United Kingdom, products, regardless of their origin, practical difficulties in finding out, first, be it national or foreign, the whether the laws of the exporting State requirement of a prior examination give equivalent protection, and secondly, by the public health authority and whether those laws have been properly of a statement on the packaging applied to the imported product, make indicating that approval has been the measures to be adopted by the granted for the product to be put importing State necessary and pro- on the market, does not constitute a portional to the risk to public health quantitative restriction on imports." from the imported product.
The United Kingdom considers, 6. Observations of the United Kingdom therefore, that, in view of those problems and the absence of harmonization in this field, the full exercise of the Member The arguments of the United Kingdom States' powers remains unaffected, as is are in similar vein to those of the stated in the Opinion of Mr Advocate Netherlands, Danish and Italian General Mayras in Case 244/78 Union Governments. It agrees that the problem Laitière Normande [1979] ECR 2663. raised by this case is the proper interpret- ation of Article 36 of the Treaty and the The United Kingdom concludes by scope of the powers reserved by the stating that it would be particularly Treaty to the Member States to protect concerned at the possibility of seeing the health of their citizens. Member States exposed to serious disease hazards if the interpretation, The United Kingdom observes that sought by the appellant in the main Article 36 enables a Member State to proceedings, of what constitutes restrict imports to protect public health permissible prohibitions or restrictions on within its frontiers and to restrict exports imports in this sphere were accepted. to protect public health elsewhere in the Community. III — O r a l p r o c e d u r e According to the United Kingdom the criteria justifying the restrictive measures should be: At the sitting on 1 July 1981 oral argument was presented by the following: A. Bos, acting as Agent, with 1. whether they are imposed for the Mr Van der Kolk, appearing as expert, protection of public health; and for the Netherlands Government; L. Mikaelsen, acting as Agent for the 2. whether they are compatible with Danish Government; and R. Wägenbaur, Article 36 and fall within the limits set a member of the Legal Department of by the decisions of the Court. the Commission of the European Communities, acting as Agent, assisted by T. Van Rijn, with M. Hudson, The United Kingdom states, moreover, appearing as expert, for the Commission that parallel or similar requirements in of the European Communities. any two Member States may not of themselves provide the same degree of The Advocate General delivered her protection for public health in both opinion at the sitting on 14 October States. 1981.
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Decision
1 By judgment of 29 October 1980, which was received by the Court on 10 December 1980, the Gerechtshof [Regional Court of Appeal], The Hague, referred to the Court for a preliminary ruling under Article 177 of the EEC Treaty a question relating to the interpretation of Articles 30 and 36 of the EEC Treaty so as to enable it to determine whether the Netherlands legislation relating to the approval of plant protection products is compatible with Community law.
2 This question was raised in the course of an appeal against the sentence, imposed at first instance, fining Frans-Nederlandse Maatschaapij voor Biologische Produkten BV for an offence contrary to the first paragraph of Article 2 of the Bestrijdingsmiddelenwet [Law relating to plant protection products], 1962, which prohibits the sale, storage or use as a plant protection product of a product which has not been approved pursuant to that Law.
3 The company concerned had imported, sold or supplied in the Netherlands a quantity of a plant protection product called "Fumicot Fumispore", containing as an active substance a toxic product, parahydroxyphenyl-sali- cylamide. That plant protection product had already been lawfully marketed in France but had not received the approval which is required in the Netherlands in accordance with the above-mentioned Law.
4 The system of approval in force in the Netherlands was established by the Law of 1962 in order to protect public health. That system prohibits, in principle, the use of such products without prior approval. The conditions for approval relate to the composition, effectiveness and harmlessness of those products as well as to the information for users set out on their packaging. The costs relating to laboratory examinations were, under the legislation in force at the time of the alleged offences, to be borne by the applicant.
FRANS-NEDERLANDSE MAATSCHAPPIJ VOOR BIOLOGISCHE PRODUCTEN
5 The company concerned has contended that the system of approval in question is incompatible with the provisions of Community law prohibiting quantitative restrictions on imports and measures having equivalent effect, and that therefore a prosecution brought under that system cannot be well founded.
6 To enable it to decide this issue, the Gerechtshof has referred the following question to the Court:
"Is the scheme of the Netherlands Law of 1962 relating to plant protection products compatible with Article 30 of the EEC Treaty in so far as that Law prohibits the marketing in the Netherlands of a product originating in another Member State in which that product has been lawfully marketed and in which it meets the legislative requirements which protect the same overriding requirements of public health as the Netherlands Law?"
7 The Commission maintains that so long as no recognition of approvals in the field of plant protection products has been established at Community level, Member States are free to prohibit, in the interests of public health, the importation and marketing of such products originating in another Member State in which they have been lawfully marketed.
8 The Danish, Italian and Netherlands Governments and the United Kingdom emphasize the dangers which those products are capable of causing to health and the environment in general and draw attention to the differences in controls which result in particular from the diversity of climatic conditions. Without denying that such national rules may constitute an obstacle to trade between Member States, they consider that rules of that kind are lawful under the exception provided for by Article 36 of the EEC Treaty in the case of the overriding considerations of the protection of public health.
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9 Whilst it is not for the Court, in proceedings brought under Article 177 of the EEC Treaty, to pronounce upon the compatibility of rules of national law with provisions of Community law, it does have jurisdiction to provide the national court with all material concerning the interpretation of Community law which will enable that court to judge whether those rules are compatible with the rule of Community law in question. The question should therefore be construed as asking, essentially, whether, and if so to what extent, the system and the detailed procedures governing the approval of plant protection products are justified in the light of the requirements of Articles 30 and 36 of the EEC Treaty.
10 Although the question, as put to the Court, merely concerns the interpre- tation of Article 30 of the Treaty, it is necessary, for the purpose of answering it, to consider the system which emerges from the general rule laid down by that article in conjunction with the derogation from it contained in Article 36 of the Treaty.
1 1 Under Article 30 of the EEC Treaty quantitative restrictions on imports as well as all measures having equivalent effect between Member States are prohibited. That general rule, however, includes a reference, in particular, to Article 36, according to which the provisions of Articles 30 to 34 are not to preclude prohibitions or restrictions on imports which are justified inter alia on grounds of "the protection of health and life of humans, animals or plants". The last sentence of Article 36 states, however, that "such prohibitions or restrictions shall, however, not constitute a means of arbitrary discrimination or a disguised restriction on trade between Member States."
12 It should be noted that, at the time of the alleged offences, there were no common or harmonized rules relating to the production or marketing of plant protection products. In the absence of harmonization, it was therefore for the Member States to decide what degree of protection of the health and life of humans they intended to assure and in particular how strict the checks to be carried out were to be (judgment of the Court of 20 May 1976 in Case 104/75 De Peijper [1976] ECR 613 at p. 635), having regard however to the fact that their freedom of action is itself restricted by the Treaty.
FRANS-NEDERLANDSE MAATSCHAPPIJ VOOR BIOLOGISCHE PRODUCTEN
1 3 In that respect, it is not disputed that the national rules in question are intended to protect public health and that they therefore come within the exception provided for by Article 36. The measures of control applied by the Netherlands authorities, in particular as regards the approval of the product, may not therefore be challenged in principle. However, that leaves open the question whether the detailed procedures governing approvals, as indicated by the national court, may possibly constitute a disguised restriction, within the meaning of the last sentence of Article 36, on trade between Member States, in view, on the one hand, of the dangerous nature of the product and, on the other hand, of the fact that it has been the subject of a procedure for approval in the Member State where it has been lawfully marketed.
1 4 Whilst a Member State is free to require a product of the type in question, which has already received approval in another Member State, to undergo a fresh procedure of examination and approval, the authorities of the Member States are nevertheless required to assist in bringing about a relaxation of the controls existing in intra-Community trade. It follows that they are not entitled unnecessarily to require technical or chemical analyses or laboratory tests where those analyses and tests have already been carried out in another Member State and their results are available to those authorities, or may at their request be placed at their disposal.
15 For the same reasons, a Member State operating an approvals procedure must ensure that no unnecessary control expenses are incurred if the practical effects of the control carried out in the Member State of origin satisfy the requirements of the protection of public health in the importing Member State. On the other hand, the mere fact that those expenses weigh more heavily on a trader marketing small quantities of an approved product than on his competitor who markets much greater quantities, does not justify the conclusion that such expenses constitute arbitrary discrimination or a disguised restriction within the meaning of Article 36.
16 The reply to be given to the question submitted to the Court must therefore be that it follows from Article 30 in conjunction with Article 36 of the Treaty that a Member State is not prohibited from requiring plant protection
JUDGMENT OF 17. 12. 1981 — CASE 272/80
products to be subject to prior approval, even if those products have already- been approved in another Member State. The authorities of the importing State are however riot entitled unnecessarily to require technical or chemical analyses or laboratory tests when the same analyses and tests have already- been carried out in another Member State and their results are available to those authorities or may at their request be placed at their disposal.
17 It is for the national court to examine, in the light of the foregoing considerations, whether, and if so to what extent, the procedures governing approvals laid down by the national legislation are justified under Article 36.
Costs
18 The costs incurred by the Governments of Denmark, Italy and the Netherlands, by the United Kingdom and by the Commission of the European Communities, which have submitted observations to the Court, are not recoverable. As the proceedings are, so far as the parties to the main proceedings are concerned, in the nature of a step in the proceedings pending before the national court, the decision on costs is a matter for that court.
On those grounds,
THE COURT,
in answer to the question referred to it by the Gerechtshof, The Hague, by judgment of 29 October 1980, registered at the Court on 10 December 1980, hereby rules :
It follows from Article 30 in conjunction with Article 36 of the Treaty that a Member State is not prohibited from requiring plant protection products to be subject to prior approval, even if those products have already been approved in another Member State. The authorities of the importing State are however not entitled unnecessarily to require
FRANS-NEDERLANDSE MAATSCHAPPIJ VOOR BIOLOGISCHE PRODUCTEN
technical or chemical analyses or laboratory tests when the same analyses or tests have already been carried out in another Member State and their results are available to those authorities or may at their request be placed at their disposal.
Mertens de Wilmars Bosco Due Touffait Pescatore Mackenzie Stuart O'Keeffe Koopmans Everling Chloros Grévisse
Delivered in open court in Luxembourg on 17 December 1981.
A. Van Houtte J. Mertens de Wilmars Registrar President
OPINION OF MRS ADVOCATE GENERAL ROZES DELIVERED O N 14 OCTOBER 1981 '
Mr President, a fungicide called "Fumicot Fumispore" Members of the Court, to a company in Groningen which used it to disinfect its sugar silo. This product is intended to eliminate any trace of This reference for a preliminary ruling mouldiness remaining in the air in which concerns once again the interpret- premises used for the production and ation of Articles 30 and 36 of the Treaty storage of foodstuffs and is used mainly arises out of criminal proceedings in dairies, in premises used for making brought in the Netherlands against cheese and in bakeries. Frans-Nederlandse Maatschappij voor Biologische Producten BV, an importer The disinfectant has been approved in of French plant protection products. France, where it is manufactured, in accordance with the rules in force (Law I — (a) That company is being pros- No 525 of 2 November 1943, as ecuted for having sold in February 1978 amended, relating to the organization 1 — Translated from the French.