Commission Regulation (EC) No 2229/2004 of 3 December 2004 laying down further detailed rules for the implementation of the fourth stage of the programme of work referred to in Article 8(2) of Council Directive 91/414/EECText with EEA relevance
2229/2004 • 32004R2229
Legal Acts - Regulations
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24.12.2004
EN
Official Journal of the European Union
L 379/13
COMMISSION REGULATION (EC) No 2229/2004
of 3 December 2004
laying down further detailed rules for the implementation of the fourth stage of the programme of work referred to in Article 8(2) of Council Directive 91/414/EEC
(Text with EEA relevance)
THE COMMISSION OF THE EUROPEAN COMMUNITIES,
Having regard to the Treaty establishing the European Community,
Having regard to Council Directive 91/414/EEC of 15 July 1991 concerning the placing of plant protection products on the market (1), and in particular the second subparagraph of Article 8(2) thereof,
Whereas:
(1)
Directive 91/414/EEC provides for the Commission to undertake a programme of work within a period of 12 years (the programme of work) following the notification of that Directive for the gradual examination of active substances on the market two years after the date of notification of that Directive.
(2)
Commission Regulation (EEC) No 3600/92 of 11 December 1992 laying down the detailed rules for the implementation of the first stage of the programme of work referred to in Article 8(2) of Council Directive 91/414/EEC concerning the placing of plant protection products on the market (2) provides for the first stage of the programme of work and is still ongoing.
(3)
Commission Regulation (EC) No 451/2000 of 28 February 2000 laying down the detailed rules for the implementation of the second and third stages of the work programme referred to in Article 8(2) of Council Directive 91/414/EEC (3) provides for the second stage of the programme of works and is also ongoing.
(4)
Regulation (EC) No 451/2000 also provides for a third stage of the programme of works for an additional number of active substances not covered by the first and second stages of the programme. Commission Regulation (EC) No 1490/2002 of 14 August 2002 laying down further detailed rules for the implementation of the third stage of the programme of work referred to in Article 8(2) of Council Directive 91/414/EEC and amending Regulation (EC) No 451/2002 (4) also provides for the third stage of the programme of works. The third stage is also ongoing.
(5)
Commission Regulation (EC) No 1112/2002 of 20 June 2002 laying down the detailed rules for the implementation of the fourth stage of the programme of work referred to in Article 8(2) of Council Directive 91/414/EEC (5) provides for the fourth stage of work and is ongoing. Producers wishing to support the inclusion of the active substances covered by that stage in Annex I to Directive 91/414/EEC have undertaken to provide the necessary information.
(6)
By reason of the accession of the Czech Republic, Estonia, Cyprus, Latvia, Lithuania, Hungary, Malta, Poland, Slovenia and Slovakia, it is necessary to provide the opportunity for producers in those new Member States to notify their interest to participate in stage four of the programme of work for all substances covered under that stage. It is also appropriate to organise the review of substances that were on the market in a new Member State before 1 May 2004 and which are not included in stages one to four of the programme of work.
(7)
The procedures established in this Regulation should not prejudice procedures and actions to be undertaken in the framework of other Community legislation, in particular under Council Directive 79/117/EEC of 21 December 1978 prohibiting the placing on the market and use of plant protection products containing certain active substances (6), where information becomes available to the Commission showing that its requirements may be satisfied.
(8)
Regulation (EC) No 178/2002 of the European Parliament and of the Council of 28 January 2002 laying down the general principles and requirements of food law, establishing the European Food Safety Authority and laying down procedures in matters of food safety (7) created the European Food Safety Authority (EFSA) to ensure that the Community has access to high-quality, independent and efficient scientific and technical support in order to achieve a high level of health protection in relation to legislation concerning safety of food and feed. It is therefore appropriate to provide that the EFSA should have a role in the programme of work on active substances.
(9)
The relationships between producers, Member States, the Commission and the EFSA and the obligations on each of them for the implementation of the programme of work should be laid down, taking into account experience gained during the first and second stages of the programme of work, the objective of separating risk assessment from risk management and the need to organise the work in the most efficient way.
(10)
Close cooperation between producers, Member States, the Commission and the EFSA and a scrupulous respect of time limits laid down is necessary to ensure the efficiency of the programme of work. Strict time limits for all elements of the fourth stage of that programme should be set in order to ensure its finalisation within an acceptable time period. For certain active substances where the dossier requirements are limited, a short deadline for submission of the dossier is appropriate in order to allow the opportunity for further information to be provided within the overall time-frame for completion of the review programme.
(11)
In order to avoid duplication of work, and in particular experiments involving vertebrate animals, producers should be encouraged to submit collective dossiers.
(12)
It is necessary to define the obligations of producers with regard to the formats, time periods and national authorities and the EFSA for the information to be submitted. Many of the active substances covered by stage four of the programme of work are produced in small volume for specialist purposes. Some are important in organic or other low input farming systems and may be expected to constitute a low risk in terms of human and environmental protection.
(13)
The Commission identified in its progress Report to the European Parliament and the Council — Evaluation of the active substances of plant protection products (submitted in accordance with Article 8(2) of Council Directive 91/414/EEC on the placing of plant protection products on the market) (8) the need for special measures to be adopted in relation to low-risk compounds.
(14)
A modified approach is required for this stage of the programme of work to reduce the risk that large numbers of active substances will be withdrawn for economic reasons alone. For certain groups of active substances it is, therefore, appropriate that the format and requirements for the information to be submitted are different from those developed for active substances in the previous three stages of the programme of work.
(15)
In the interests of consistency of Community legislation it is necessary to ensure that the measures provided for in this Regulation are coherent with measures taken under Directive 98/8/EC of the European Parliament and of the Council of 16 February 1998 concerning the placing of biocidal products on the market (9).
(16)
The notification and submission of a dossier should not be a prerequisite for the possibility, after inclusion of the active substance in Annex I to Directive 91/414/EEC, to place plant protection products on the market subject to the provisions of Article 13 of that Directive. Therefore persons who have not submitted notifications should be able to be informed at all stages of the evaluation process of the possible further requirements for continued marketing of plant protection products containing an active substance under evaluation.
(17)
In order to ensure that all relevant information on the potentially dangerous effects of an active substance or its residues are considered, technical or scientific information submitted within the relevant time limits by any person should also be taken into consideration in the evaluations.
(18)
Where cooperation with notifiers ceases, it is impossible to continue further evaluation efficiently and therefore the evaluation of an active substance should be terminated unless a Member State takes over.
(19)
The task of evaluation should be distributed among the competent authorities of the Member States. Therefore, for each active substance a rapporteur Member State should be designated. Where appropriate the rapporteur Member State should assess the completeness checklist provided by the notifier, and examine and evaluate the information submitted. It should present to the EFSA the results of the evaluation and make a recommendation to the Commission concerning the decision to be taken with regard to the active substance concerned. For certain groups of active substances it is appropriate that the rapporteur Member States closely cooperate with other rapporteur Member States for that group. For each group it is appropriate to identify a lead rapporteur to coordinate such cooperation.
(20)
Rapporteur Member States should send draft assessment reports of their evaluations of active substances to the EFSA. The draft assessment reports should be peer reviewed by the EFSA before they are submitted to the Commission.
(21)
In case of an apparent imbalance in the responsibilities borne by the Member States as rapporteur in the evaluation and assessment, it should be possible to replace the Member State originally designated as rapporteur for a particular active substance by another Member State.
(22)
To ensure the proper resourcing of this stage of the programme of work, a fee should be paid to the Member States for the handling and evaluation of dossiers and draft assessment reports.
(23)
The EFSA has been consulted on the proposed measures.
(24)
The measures provided for in this Regulation are in accordance with the opinion of the Standing Committee on the Food Chain and Animal Health,
HAS ADOPTED THIS REGULATION:
CHAPTER I
SUBJECT MATTER AND SCOPE, DEFINITIONS AND THE DESIGNATED MEMBER STATE AUTHORITY
Article 1
Subject matter and scope
1. This Regulation lays down:
(a)
further detailed rules for the implementation of the fourth stage of the programme of work referred to in the second subparagraph of Article 8(2) of Directive 91/414/EEC (the programme of work) with respect to the continued evaluation of the active substances notified under Regulation (EC) No 1112/2002;
(b)
rules covering the active substances that were on the market before 1 May 2004 in the Czech Republic, Estonia, Cyprus, Latvia, Lithuania, Hungary, Malta, Poland, Slovenia and Slovakia and which are not included in stages one to three of the programme of work and which are not covered by Regulation (EC) No 1112/2002.
2. Article 6(2) and (3) and the second paragraph of Article 6(4) of Directive 91/414/EEC shall not apply to active substances listed in Annex I to this Regulation as long as the procedures provided for in this Regulation with regard to such substances have not been finalised.
3. This Regulation shall apply without prejudice to:
(a)
reviews by Member States of active substances listed in Annex I to this Regulation in particular pursuant to renewals of authorisations in accordance with Article 4(4) of Directive 91/414/EEC;
(b)
reviews by the Commission in accordance with Article 5(5) of Directive 91/414/EEC;
(c)
assessments carried out under Directive 79/117/EEC.
Article 2
Definitions
For the purpose of this Regulation, the definitions set out in Article 2 of Directive 91/414/EEC and Article 2 of Regulation (EC) No 1112/2002 shall apply.
The following definitions shall also apply:
(a)
‘notifier’ means the natural or legal person who has submitted a notification in accordance with:
(i)
Regulation (EC) No 1112/2002, as listed in Annex II to this Regulation, or
(ii)
Article 4 of this Regulation;
(b)
‘rapporteur Member State’ means the rapporteur Member State for the active substance as set out in Annex I.
(c)
‘summary dossier’ means a dossier containing the information required under Article 10(2), where summaries are given of the results of the tests and studies referred to in that paragraph.
(d)
‘complete dossier’ means a dossier containing the information required under Article 10(3), where the results of the tests and study reports referred to in the summary dossier are given in full.
Article 3
Designated Member State authority
1. Each Member State shall designate an authority or authorities to carry out the obligations of the Member States as defined in this Regulation.
2. The national authorities listed in Annex III shall coordinate and ensure all necessary contacts with notifiers, other Member States, the Commission and the European Food Safety Authority (EFSA) in accordance with this Regulation.
Each Member State shall give the details concerning the designated coordinating national authority to the Commission, the EFSA and the designated coordinating national authority of each other Member State and inform them of any modifications thereof.
CHAPTER II
NOTIFICATIONS BY PRODUCERS IN NEW MEMBER STATES OF ACTIVE SUBSTANCES
Article 4
Notifications by producers in new Member States
1. Any producer in a new Member State referred to in Article 1(1)(b) of this Regulation wishing to secure the inclusion in Annex I to Directive 91/414/EEC of an active substance listed in Annex I to this Regulation shall notify the details set out in Annex V of this Regulation to the Commission, other notifiers for that substance and the rapporteur Member State at the latest three months from the date of entry into force of this Regulation.
2. Any producer making a notification under paragraph 1 shall fulfil the obligations of producers or notifiers set out in this Regulation for the active substance notified.
3. Where a producer in a new Member State has not submitted a notification for an active substance listed in Annex I to this Regulation, in accordance with paragraph 1, it shall only be permitted to participate in the programme of work collectively with one or more notifiers of the active substance, including a Member State which has notified in accordance with paragraph 4 of this Article.
4. Where no notification has been received for an active substance listed in Annex I to this Regulation, a new Member State may declare its interest in supporting the inclusion of that active substance in Annex I to Directive 91/414/EEC by notifying the Commission and the rapporteur Member State.
That notification must be submitted as soon as possible, and no later than three months from the date the Commission has informed the Member States that no notification has been submitted for that active substance.
A Member State submitting such a notification shall thereafter be treated as the producer for the purposes of the evaluation of the active substance concerned.
5. The Commission shall decide, as provided for in the fourth subparagraph of Article 8(2) of Directive 91/414/EEC, not to include in Annex I to that Directive active substances referred to in Annex I to this Regulation for which no notification has been submitted in accordance with paragraphs 1 or 4 of this Article. The Decision shall state the reasons for the non-inclusion.
Member States shall withdraw authorisations of plant protection products containing such active substances within the period prescribed in the Decision.
CHAPTER III
CONDITIONS FOR THE SUBMISSION OF DOSSIERS OF ACTIVE SUBSTANCES AND SUBMISSION OF INFORMATION BY THIRD PARTIES
Article 5
Submission of dossiers by more than one notifier
1. Where for any active substance listed in Annex I there is more than one notifier, the notifiers concerned shall take all reasonable steps to submit the dossier for such substance collectively.
Where the dossier is not submitted by all such notifiers, it shall contain details of the efforts made and the reasons why certain notifiers have not participated in the submission of the dossier.
2. Where an active substance has been notified by more than one notifier, those notifiers shall, for each study involving vertebrate animals, give details of the attempts made to avoid duplication of testing and give, if applicable, the reasons for conducting a duplicate study.
Article 6
Submission of dossiers to the rapporteur Member State
1. The notifier shall submit the dossier for the active substance (the dossier) to the rapporteur Member State.
2. The dossier shall include the following:
(a)
a copy of the notification; in the case of a collective notification made by more than one producer as referred to in Article 5(1), it shall include:
(i)
a copy of the notifications made in accordance with Article 4 or 5 of Regulation (EC) No 1112/2002 or Article 4 of this Regulation;
(ii)
the name of the person designated by the producers concerned as being responsible for the collective notification who will act as a contact point during the procedure;
(b)
a limited range of representative uses of the active substance, in respect of which the data submitted by the notifier in the dossier shall demonstrate that for one or more preparations, the requirements set out in Article 5 of Directive 91/414/EEC for inclusion of the active substance in Annex I to that Directive may be met.
3. When requested by the rapporteur Member State as provided for in Article 20(2) to circulate the updated summary dossier or where relevant the updated complete dossier or parts thereof the notifier shall do this at the latest one month from the date of receipt of such a request.
Article 7
Dossiers for active substances submitted under Directive 98/8/EC
By derogation from Articles 5 and 6, where an active substance has been notified under Directive 98/8/EC the notifier may submit:
(a)
a copy of the dossier submitted under Directive 98/8/EC;
(b)
any additional information referred to in Annexes II and III to Directive 91/414/EEC necessary to justify the inclusion of the active substance in Annex I to that Directive by reference to uses falling within the scope of that Directive.
Article 8
Loading citations...Dossiers for active substances submitted under Regulation (EC) No 1490/2002
Where a dossier has been submitted under Regulation (EC) No 1490/2002, the person who submitted that dossier may submit, together with the further dossier submitted under this Regulation:
(a)
a reference to the dossier submitted under Regulation (EC) No 1490/2002;
(b)
any additional information referred to in Annexes II and III to Directive 91/414/EEC necessary to justify the inclusion of the active substance in Annex I to that Directive by reference to uses falling within the scope of this Regulation.
Article 9
Specific conditions for submissions of dossiers for active substances listed in Part A of Annex I
1. Where the dossier concerns an active substance listed in Part A of Annex I, in addition to the information required under Article 5 and Article 6(2), the notifier shall submit the following information concerning the active substance and the plant protection product (where applicable):
(a)
all available information on possible risks to human and animal health and the environment including that available from searching the literature and identifying the data bases searched and search terms used;
(b)
available assessment reports from any OECD country;
(c)
for any ongoing tests and studies not yet fully completed, information on those tests and studies and a projected date of completion.
2. The dossier shall physically contain the individual test and study reports containing all the information referred to in paragraph 1.
3. Each Member State shall specify the number of copies of the dossier to be submitted by the notifier when it is acting as a rapporteur and when it receives copies under Article 20(2).
The format of the dossier shall take account of the recommendations made in accordance with the procedure referred to in Article 19 of Directive 91/414/EEC.
Article 10
Specific conditions for submissions of dossiers for active substances listed in Parts B to G of Annex I
1. Where the dossier concerns an active substance listed in Part B to G of Annex I, the notifier shall submit a dossier and a summary dossier.
2. The notifier(s) shall include in the summarydossier:
(a)
the information required under Article 5 and Article 6(2) of this Regulation;
(b)
for each point of Annex II (Part A or Part B as appropriate) to Directive 91/414/EEC and for each point of Annex III (Part A or Part B as appropriate) to that Directive, the summaries and results of tests and studies and the name of the person or institute that has carried out those tests and studies;
(c)
a checklist to be filled in by the notifier, demonstrating that the dossier is complete in accordance with Article 18 of this Regulation.
The tests and studies as referred to in paragraph 2(b) of this Article shall be those relevant to the assessment of the criteria referred to in Article 5 of Directive 91/414/EEC for one or more preparations for the uses taking into account the fact that data gaps in the dossier as regards the information required under Annex II of Directive 91/414/EEC, resulting from the proposed limited range of representative uses of the active substance, may lead to restrictions in the inclusion in Annex I of Directive 91/414/EEC.
3. The complete dossier shall physically contain the individual test and study reports concerning all the information referred to in point (b) and the second subparagraph of paragraph 2.
4. Each Member State shall specify the number of copies and the format of the summary and the complete dossiers to be submitted by the notifiers.
In defining the format of the complete and summary dossiers Member States shall take account of the recommendations made in accordance with the procedure referred to in Article 19 of Directive 91/414/EEC.
Article 11
Submission of information by third parties
Any natural or legal person wishing to submit relevant information which may contribute to the evaluation of an active substance listed in Annex I, in particular with regard to the potentially dangerous effects of that substance or its residues on human and animal health and on the environment, shall do so by the relevant time limit set out in Article 12.
Such information shall be submitted to the rapporteur Member State and the EFSA. When requested by the rapporteur Member State such person shall also submit that information to the other Member States at the latest one month from the date of receipt of such a request.
Article 12
Time limits for submission of dossiers
The notifier(s) shall submit the dossier to the relevant rapporteur Member State by:
(a)
30 June 2005 at the latest for the active substances listed in Part A of Annex I;
(b)
30 November 2005 at the latest for the active substances listed in Parts B to G of Annex I.
Article 13
Non-submission of dossiers
1. Where the notifier does not submit the dossier or any part thereof within the relevant time limit set out in Article 12, the rapporteur Member State shall inform the Commission and the EFSA within two months of the date of expiry of the time limit, giving any justification for the delay provided by the notifiers.
2. On the basis of the information submitted by the rapporteur Member State in accordance with paragraph 1, the Commission shall determine whether the notifier has demonstrated that the delay in the submission of the dossier was caused by force majeure.
In that case, it shall establish a new time limit for the submission of a dossier fulfilling the relevant requirements of Articles 5, 6, 9, and 10 of this Regulation in accordance with the procedure referred to in Article 19 of Directive 91/414/EEC.
3. The Commission shall decide, as provided for in the fourth subparagraph of Article 8(2) of Directive 91/414/EEC, not to include in Annex I to that Directive an active substance for which no dossier has been submitted within the time limit provided for in Article 12 of this Regulation or the second subparagraph of paragraph 2 of this Article. The Decision shall state the reasons for the non-inclusion.
Member States shall withdraw authorisations of plant protection products containing such active substances within the period prescribed in the Decision.
Article 14
Replacement or withdrawal of notifier
1. If a notifier decides to end its participation in the programme of work for an active substance, it shall immediately inform the rapporteur Member State, the Commission, the EFSA and all other notifiers of the active substance concerned of its decision, giving the reasons.
Where a notifier ends its participation or fails to fulfil its obligations under this Regulation, the procedures provided for in Articles 15 to 24 shall be terminated as regards its dossier.
2. If a notifier agrees with another producer that the notifier shall be replaced for the purposes of further participation in the programme of work under this Regulation, the notifier and such other producer shall inform the rapporteur Member State, the Commission and the EFSA by a common declaration agreeing that such other producer shall replace the original notifier in carrying out the notifier’s duties pursuant to the relevant provisions of Articles 4, 5, 6, 9, 10, 12 and 24. They shall ensure that the other notifiers for the substance concerned are informed at the same time.
The other producer in this case shall be jointly liable with the original notifier for any fees remaining payable in relation to the notifier's application under the regime established by Member States pursuant to Article 30.
3. If all notifiers for an active substance end their participation in the programme of work a Member State may choose to act as notifier for the purposes of further participation in the programme of work.
Any Member State wishing to act as a notifier shall inform the rapporteur Member State, the Commission and the EFSA at the latest one month from the date of being informed that all notifiers have decided to end their participation and shall replace the original notifier in carrying out the notifier’s duties pursuant to the relevant provisions of Articles 4, 5, 6, 9, 10, 12 and 24.
4. All information submitted shall remain available to the rapporteur Member States, the Commission and EFSA
CHAPTER IV
EVALUATIONS OF DOSSIERS
Article 15
General Conditions for evaluations of dossiers
1. Without prejudice to Article 18 the rapporteur Member State shall evaluate all dossiers submitted to it.
2. Without prejudice to Article 7 of Directive 91/414/EEC, the rapporteur Member State shall not accept the submission of new studies during the evaluation except as provided for in Article 9 (1)(c) of this Regulation.
However, the rapporteur Member State may request the notifier to submit further data which are necessary to clarify the dossier. When doing so the rapporteur Member State shall set a time limit within which the information shall be provided. The time limit shall not affect the time limit for the submission of the draft assessment report by the rapporteur Member State to the EFSA as provided for in Article 21(1) or Article 22(1).
3. The rapporteur Member State may, from the start of the evaluation of the dossier:
(a)
consult with experts from the EFSA;
(b)
request additional technical or scientific information from other Member States to assist in the evaluation.
4. Notifiers may seek specific advice from the rapporteur Member State.
Article 16
Cooperation between Member States
1. The rapporteur Member States shall cooperate in the evaluation within each group set out in Annex I and shall organise such cooperation in the most effective and efficient way.
2. The rapporteur Member State identified within each group in Annex I as the ‘lead rapporteur’ shall take a lead in organising that cooperation and in organising the provision of advice to notifiers where it concerns matters of general interest to the other Member States concerned.
Article 17
Specific condition for evaluations of active substances listed in Part A of Annex I
Where possible and where it does not affect the time limit for the submission of the draft assessment report as provided for in Article 21(1), the rapporteur Member State shall evaluate further information identified under Article 9(1)(c) subsequently provided by the notifier.
Article 18
Completeness check of dossiers for substances listed in Parts B to G of Annex I
1. The rapporteur Member State shall assess the checklists provided by the notifiers in accordance with Article 10(2)(c).
2. The rapporteur Member State shall at the latest three months from the date of receipt of all dossiers for an active substance report to the Commission on the completeness of the dossiers.
3. For those active substances for which one or more dossiers are considered to be complete, the rapporteur Member State shall perform the evaluation as referred to in Articles 15 and 19, unless the Commission informs the rapporteur Member State, within two months of the date of receipt of the report of the rapporteur Member State on completeness, that it does not consider the dossier to be complete.
4. For those active substances for which a rapporteur Member State or the Commission consider that no dossier is complete within the meaning of Articles 5, 6 and 10, the Commission shall, within three months from the date of the receipt of the report of the rapporteur Member State on completeness, refer such a report to the Standing Committee for the Food Chain and Animal Health.
In accordance with the procedure referred to in Article 19 of Directive 91/414/EEC it shall be decided whether a dossier is to be considered complete within the meaning of Articles 5, 6 and 10.
5. The Commission shall decide, as provided for in the fourth subparagraph of Article 8 (2) of Directive 91/414/EEC, not to include in Annex I to Directive 91/414/EEC an active substance for which no complete dossier has been submitted within the time limit provided for in Article 12 of this Regulation or the second sub-paragraph of Article 13 (2).
Article 19
Specific conditions for evaluations of dossiers for substances listed in Parts B to G of Annex I
1. Where active substances listed in Part D of Annex I to this Regulation have been evaluated under Directive 98/8/EC those evaluations shall be taken into account, where relevant, for the purposes of this Regulation
2. Where active substances have been evaluated under a former stage of the programme of work referred to in Article 8(2) of Directive 91/414/EEC those evaluations shall be taken into account, where relevant, for the purposes of this Regulation.
3. The rapporteur Member State shall evaluate and report only on those active substances for which at least one dossier has been determined to be complete in accordance with Articles 5, 6, and 10. For dossiers concerning the same active substance not determined to be complete, it shall check whether the identity and impurities of the active substance in those dossiers are comparable to the identity and impurities of the active substance in the dossiers considered complete. It shall record its views on this point in the draft assessment report.
The rapporteur Member State shall take into consideration the information available on potentially dangerous effects in the other dossiers submitted by any notifier or by any third party in accordance with Article 11.
Article 20
General conditions for draft Assessment Reports
1. The draft assessment report shall be submitted as far as possible in the format recommended in accordance with the procedure referred to in Article 19 of Directive 91/414/EEC.
2. The rapporteur Member State shall request the notifiers to submit an updated summary dossier to the EFSA, the other Member States and on request to the Commission at the same time as the rapporteur's draft assessment report is sent to the EFSA.
The Member States, the Commission or the EFSA may request through the rapporteur Member State that notifiers also send them an updated complete dossier or parts thereof. The notifier shall provide any such updated dossier by the date specified in the request.
Article 21
Specific conditions for draft Assessment Reports and Recommendations to the Commission for active substances listed in Part A of Annex I
1. The rapporteur Member State shall send the draft assessment report to the EFSA as quickly as possible, and 12 months from the date of expiry of the time limit provided for in Article 12(a) at the latest.
2. The rapporteur Member State shall include in the draft assessment report a reference to each test or study concerning each point of Annex II (Part A or Part B as appropriate) to Directive 91/414/EEC and for each point of Annex III (Part A or Part B as appropriate) to that Directive relied on for the assessment.
That reference shall be made in the form of a list of test and study reports including the title, the author(s), the date of the study or test report and the date of publication, the standard to which the test or study was conducted, the holder’s name, and if any, the claim made by the holder or notifier for data protection.
3. At the same time as the rapporteur Member State sends its assessment report to the EFSA as provided for in paragraph 1, it shall make a recommendation to the Commission:
(a)
either to include the active substance in Annex I to Directive 91/414/EEC stating where appropriate the proposed conditions for inclusion; such conditions:
(i)
may include the time limit for such inclusion:
(ii)
shall state whether any information is required, whether such additional information is included in the tests and studies referred to in Article 9(1)(c) of this Regulation and if so, the probable timetable for the provision of such information; or
(b)
not to include the active substance in Annex I to Directive 91/414/EEC, stating the proposed reasons for the non-inclusion.
4. In addition to the conditions for inclusion proposed under paragraph 2(a) of this Article, the rapporteur Member State may indicate if it has identified, for the proposed limited range of representative uses mentioned in the dossier, any information missing from the dossier which may be required by Member States as confirmatory information when they come to grant authorisations under Article 4 of Directive 91/414/EEC for plant protection products containing that active substance.
Article 22
Specific conditions for draft Assessment Reports and Recommendations to the Commission for active substances listed in Parts B to G of Annex I
1. The rapporteur Member State shall send a draft assessment report to the EFSA as quickly as possible, and at the latest 12 months from the date the dossier was determined to be complete in accordance with Article 18(2).
2. The rapporteur Member State shall include in the draft assessment report a reference to each test or study concerning each point of Annex II (Part A or Part B as appropriate) to Directive 91/414/EEC and for each point of Annex III (Part A or Part B as appropriate) to that Directive relied on for the assessment.
That reference shall be made in the form of a list of test and study reports including the title, the author(s), the date of the study or test report and the date of publication, the standard to which the test or study was conducted, the holder’s name and, if any, the claim made by the holder or notifier for data protection.
3. At the same time as the rapporteur Member State sends its assessment report to the EFSA as provided for in paragraph 1, it shall make a recommendation to the Commission:
(a)
either to include the active substance in Annex I to Directive 91/414/EEC, stating the reasons for the inclusion;
(b)
or not to include the active substance in Annex I to Directive 91/414/EEC, stating the reasons for the non-inclusion.
Article 23
Replacement of rapporteur Member State
1. A rapporteur Member State shall inform the Commission and the EFSA as soon as it becomes clear that it will be unable to comply with the time limits set out in Articles 21(1) and 22(1) for the submission of the draft assessment report to the EFSA and give the reasons for the delay.
2. It may be decided to replace a rapporteur Member State for a particular active substance by another Member State where:
(a)
during the assessment and evaluation provided for in Articles 15, 16, 17 and 19 it becomes apparent that there is an imbalance in the responsibilities borne and the work to be done or actually done by the Member States as rapporteurs; or
(b)
it is clear that a Member State is unable to fulfil its obligations under this Regulation.
Such replacement shall be decided in accordance with the procedure referred to in Article 19 of Directive 91/414/EEC.
3. Where it has been decided to replace a rapporteur Member State the original rapporteur Member State shall immediately after such a decision has been taken inform the notifiers concerned and shall transfer to the newly designated rapporteur Member State all correspondence and information which it has received as rapporteur Member State for the active substance concerned.
The original Member State shall return to the notifier the part of the fee referred to in Article 30 which has not been used. The newly designated rapporteur Member State may require the payment of a further fee in accordance with Article 30.
Article 24
Evaluation by the EFSA
1. The EFSA shall, within 30 days of the date of receipt of the draft assessment report as provided for in Article 21(1) or Article 22(1) of this Regulation, check that it clearly complies with the format recommended in accordance with the procedure referred to in Article 19 of Directive 91/414/EEC.
In exceptional cases where the draft assessment report clearly does not fulfil those requirements the Commission shall agree with the EFSA and the rapporteur Member State on a period for resubmission of an amended report which shall not exceed three months.
2. The EFSA shall circulate the draft assessment report to the other Member States and to the Commission and may organise a consultation of experts including the rapporteur Member State.
3. The EFSA may consult some or all of the notifiers of active substances referred to in Annex I on the draft assessment report or parts thereof on the relevant active substances.
4. Without prejudice to Article 7 of Directive 91/414/EEC, submission of new studies shall not be accepted by the EFSA after receipt of the draft assessment report referred to in paragraph 1 of this Article.
However, the rapporteur Member State, with the agreement of the EFSA, may request the notifiers to submit within specified time limits further data considered by the rapporteur Member State or the EFSA necessary to clarify the dossier.
5. The EFSA shall make available at specific request or keep available for consultation by any person the following:
(a)
the draft assessment report, except the elements thereof which have been accepted as confidential in accordance with Article 14 of Directive 91/414/EEC;
(b)
the list of any data required for the evaluation of the possible inclusion of the active substance in Annex I to Directive 91/414/EEC, as finalised by the EFSA.
6. The EFSA shall evaluate the draft assessment report and submit its evaluation to the Commission on whether the active substance may be expected to meet the requirements of Article 5(1) of Directive 91/414/EEC at the latest one year from the date on which it has received both the dossier from the notifier, under Article 15(3) of this Regulation, and also the draft assessment report checked for compliance in accordance with paragraph 1 of this Article.
Where appropriate, the EFSA shall give its evaluation of the available options claimed to meet the requirements of Article 5(1) of Directive 91/414/EEC and any data requirements identified.
The Commission and the EFSA shall agree on a schedule for the submission of the evaluation in order to facilitate the planning of the work. The Commission and the EFSA shall also agree on the format of the evaluation.
CHAPTER V
PRESENTATION OF A DRAFT DIRECTIVE OR DRAFT DECISION CONCERNING ACTIVE SUBSTANCES AND FINALISED REVIEW REPORT
Article 25
Presentation of a draft Directive or draft Decision
1. The Commission shall present a draft review report at the latest four months from the date of receipt of the EFSA evaluation provided for in Article 24(6)
2. Without prejudice to any proposal it may submit with a view to amending the Annex to Directive 79/117/EEC, and on the basis of the finalised review report provided for in Article 26 of this Regulation, the Commission shall present to the Standing Committee on the Food Chain and Animal Health:
(a)
a draft Directive to include the active substance in Annex I to Directive 91/414/EEC stating where appropriate the conditions for inclusion; such conditions may include the time limit for such inclusion; or
(b)
a draft Decision addressed to the Member States pursuant to the fourth subparagraph of Article 8(2) of Directive 91/414/EEC, not to include that active substance in Annex I to Directive 91/414/EEC, stating the reasons for the non-inclusion and requiring the Member States to withdraw the authorisations of plant protection products containing the active substance.
The Directive or Decision shall be adopted in accordance with the procedure referred to in Article 19 of Directive 91/414/EEC.
3. In addition to the conditions for inclusion proposed under paragraph 2(a), the Commission may indicate if it has identified any information missing from the dossier which may be required by Member States when they come to grant authorisations under Article 4 of Directive 91/414/EEC.
Article 26
Finalised review report
The conclusions of the Standing Committee on the Food Chain and Animal Health, excluding any parts which refer to confidential information contained in the dossiers and determined as such in accordance with Article 14 of Directive 91/414/EEC, shall be made publicly available.
CHAPTER VI
SUSPENSION OF TIME LIMITS, MEASURES TO BE TAKEN BY MEMBER STATES AND INTERIM PROGRESS REPORTS
Article 27
Suspension of time limits
Where, in respect of an active substance listed in Annex I to this Regulation, the Commission presents a proposal for a total prohibition by way of a draft Council act based on Article 6(3) of Directive 79/117/EEC, the time limits provided for in this Regulation shall be suspended while the Council considers that proposal.
Where the Council adopts an amendment to the Annex to Directive 79/117/EEC requiring the total prohibition of that active substance, the procedure under this Regulation shall be terminated for that active substance.
Article 28
Measures taken by Member States
Any Member State which, on the basis of information contained in the dossiers referred to in Articles 5 to 10 or in the draft assessment report concerning an active substance referred to in Articles 19 to 22, intends taking action to withdraw that active substance from the market or to restrict severely the use of a plant protection product containing that active substance, shall, as soon as possible, inform the Commission, the EFSA, the other Member States and the notifiers giving the reasons for its intended action.
Article 29
Interim progress report
All Member States shall submit to the Commission and the EFSA a report of their progress on the evaluation of the active substances for which they are rapporteur. Such report shall be submitted by:
(a)
30 November 2005 for the active substances listed in Part A of Annex I;
(b)
30 November 2006 for the active substances listed in Parts B to G of Annex I.
CHAPTER VII
FEES AND OTHER CHARGES
Article 30
Fees
1. For active substances listed in Annex I Member States may establish a regime obliging the notifiers to pay a fee or charge for the administrative treatment and the evaluation of dossiers.
The income from such fees or charges shall be used to finance exclusively those costs actually incurred by the rapporteur Member State or to finance general activities of the Member States resulting from their obligations under Articles 15 to 24.
2. Member States shall establish the amount of the fee or charge referred to in paragraph 1 in a transparent manner so that it does not exceed the real cost of the examination and administrative treatment of a dossier or the general activities of the Member States resulting from their obligations under Articles 15 to 24.
However, Member States may provide for a scale of fixed charges based on average costs for the calculation of the total fee.
3. The fee or charge shall be paid in accordance with the procedure to be established by the authorities in each Member State as listed in Annex IV.
Article 31
Other charges, taxes, levies or fees
Article 30 shall be without prejudice to Member States' rights to maintain or introduce, to the extent permitted under Community law, charges, taxes, levies or fees with regard to authorisation, placing on the market, use and control of active substances and plant protection products other than the fee or charge provided for in that Article.
CHAPTER VIII
TEMPORARY AND FINAL PROVISIONS
Article 32
Temporary measures
If necessary and on a case-by-case basis, the Commission may take appropriate temporary measures as provided for by the third subparagraph of Article 8(2) of Directive 91/414/EEC for uses for which additional technical evidence has been provided demonstrating the essential need for further use of the active substance and that there is no efficient alternative.
Article 33
Entry into force
This Regulation shall enter into force on the seventh day following its publication in the Official Journal of the European Union.
This Regulation shall be binding in its entirety and directly applicable in all Member States.
Done at Brussels, 3 December 2004.
For the Commission
Markos KYPRIANOU
Member of the Commission
(1) OJ L 230, 19.8.1991, p. 1. Directive as last amended by Commission Directive 2004/71/EC (OJ L 309, 6.10.2004, p. 6).
(2) OJ L 366, 15.12.1992, p. 10. Regulation as last amended by Regulation (EC) No 2266/2000 (OJ L 259, 13.10.2000, p. 27).
(3) OJ L 55, 29.2.2000, p. 25. Regulation as last amended by Regulation (EC) No 1044/2003 (OJ L 151, 19.6.2003, p. 32).
(4) OJ L 224, 21.8.2002, p. 23. Regulation as amended by Regulation (EC) No 1744/2004 (OJ L 311, 8.10.2004, p. 23).
(5) OJ L 168, 27.6.2002, p. 14.
(6) OJ L 33, 8.2.1979, p. 36. Directive as last amended by Regulation (EC) No 850/2004 (OJ L 158, 30.4.2004, p. 7).
(7) OJ L 31, 1.2.2002, p. 1. Regulation as last amended by Regulation (EC) No 1642/2003 (L 245, 29.9.2003, p. 4).
(8) COM(2001) 444 final.
(9) OJ L 123, 24.4.1998, p. 1. Directive as last amended by Regulation (EC) No 1882/2003 (OJ L 284, 31.10.2003, p. 1).
ANNEX I
List of active substances (column A), rapporteur Member States (column B) and notifying producers (code identification) (column C) (1)
PART A
GROUP 1
LEAD RAPPORTEUR: IRELAND
Active substance
Rapporteur Member State
Notifier
(A)
(B)
(C)
Acetic acid
Germany
PAB-SE
PUN-DK
TEM-DE
Amino acids/Gamma Aminobutyric acid
Germany
AGR-ES
Amino acids/L-Glutamic acid
Germany
AGR-ES
Amino acids/L-Tryptophan
Germany
VAL-IT
Ammonium carbonate
Ireland
ABC-GB
Potassium hydrogen carbonate
Ireland
PPP-FR
Sodium hydrogen carbonate
Ireland
CLM-NL
SLY-FR
Casein
Czech Republic
3-phenyl-2-propenal (Cinnamaldehyde)
Poland
Ethoxyquin
Germany
XED-FR
Fatty acids/Decanoic acid
Ireland
PBI-GB
Fatty acids/Fatty acid methyl ester (CAS 85566-26-3)
Ireland
OLE-BE
Fatty acids/Fatty acid potassium salt
Ireland
FBL-DE
IAB-ES
NEU-DE
Fatty acids/Fatty acid potassium salt (CAS 7740-09-7)
Ireland
DKI-NL
Fatty acids/Fatty acid potassium salt (CAS 10124-65-9)
Ireland
ERO-IT
Fatty acids/Fatty acid potassium salt (CAS 13429-27-1, 2624-31-9, 593-29-3, 143-18-0, 3414-89-9, 38660-45-6, 18080-76-7)
Ireland
DXN-DK
Fatty acids/Fatty acid potassium salt (CAS 18175-44-5, 143-18-0, 3414-89-9)
Ireland
DXN-DK
Fatty acids/Fatty acid potassium salt (CAS 61788-65-6)
Ireland
TBE-ES
Fatty acids/Fatty acid potassium salt (CAS 61790-44-1)
Ireland
VAL-IT
Fatty acids/Fatty acid potassium salt (CAS 61790-44-1, 70969-43-6)
Ireland
STG-GB
Fatty acids/Fatty acid potassium salt (CAS 67701-09-1)
Ireland
CRU-IT
Fatty acids/Heptanoic acid
Ireland
DKI-NL
Fatty acids/Octanoic acid
Ireland
PBI-GB
Fatty acids/Oleic acid
Ireland
ALF-ES
Fatty acids/Pelargonic acid
Ireland
ERO-IT
NEU-DE
Fatty acids/potassium salt — decanoic acid (CAS 334-48-5)
Ireland
NSC-GB
Fatty acids/potassium salt — caprylic acid (CAS 124-07-2)
Ireland
ADC-DE
Fatty acids/potassium salt — lauric acid (CAS 143-07-7)
Ireland
NSC-GB
Fatty acids/potassium salt — oleic acid (CAS 112-80-1)
Ireland
NSC-GB
Fatty acids/potassium salt — oleic acid (CAS 112-80-1, 1310-58-3)
Ireland
BCS-DE
Fatty acids/potassium salt — oleic acid (CAS 142-18-0)
Ireland
SBS-IT
Fatty acids/potassium salt — oleic acid (CAS 143-18-0)
Ireland
VIO-GR
STG-GB
Fatty acids/potassium salt — pelargonic acid(CAS 112-05-0)
Ireland
NSC-GB
Fatty acids/potassium salt — tall oil fatty acid (CAS 61790-12-3)
Ireland
ADC-DE
Fatty acids/tall oil fatty acids (CAS 61790-12-3)
Ireland
ACP-FR
Fatty acids/Isobutyric acid
Poland
Fatty acids/Isovaleric acid
Poland
Fatty acids/Lauric acid
Ireland
Fatty acids/Valeric acid
Poland
Fatty acids/Potassium salt of natural oil acids
Poland
Formic acid
Germany
KIR-NL
Iron pyrophosphate
Slovenia
Maltodextrin
Germany
BCP-GB
Milk albumin
Czech Republic
Resins
Czech Republic
Sodium metabisulphite
Germany
ESS-IT
FRB-BE
Urea
(see also Group 6.2.)
Greece
FOC-GB
OMX-GB
Wheat gluten
Finland
ESA-NL
Propolis
Poland
GROUP 2
Group 2.1.
LEAD RAPPORTEUR: FRANCE
Active substance
Rapporteur Member State
Notifier
(A)
(B)
(C)
1-Naphthylacetamide
France
ALF-ES
AMV-GB
CFP-FR
GLO-BE
GOB-IT
HOC-GB
HRM-BE
LUX-NL
PRO-ES
SHC-FR
SPU-DE
Naphthylacetic acid
France
AIF-IT
ALF-ES
AMV-GB
CFP-FR
FIN-GB
GLO-BE
GOB-IT
HOC-GB
HRM-BE
LUX-NL
PRO-ES
RHZ-NL
SHC-FR
VAL-IT
2-Naphthyloxyacetamide
France
BCS-FR
2-Naphthyloxyacetic acid
France
AIF-IT
ASP-NL
HAS-GR
HOC-GB
SHC-FR
6-Benzyladenine
France
ALF-ES
CAL-FR
FIN-GB
GLO-BE
GOB-IT
HOC-GB
HRM-BE
NLI-AT
SUM-FR
VAL-IT
Azadirachtin
Germany
AGI-IT
ALF-ES
CAP-FR
CRU-IT
FBL-DE
IAB-ES
MAS-BE
NDC-SE
PBC-ES
PRO-ES
SIP-IT
TRF-DE
VAL-IT
Cis-Zeatin
Italy
VAL-IT
Folic acid
France
AMI-IT
CHE-DK
ISA-IT
Indolylacetic acid
France
ALF-ES
GOB-IT
RHZ-NL
Indolylbutyric acid
France
ALF-ES
BCS-FR
CRT-GB
GOB-IT
GTL-GB
HOC-GB
RHZ-NL
Gibberellic acid
Hungary
AIF-IT
ALF-ES
ALT-FR
CEQ-ES
FIN-GB
GLO-BE
HRM-BE
NLI-AT
PRO-ES
SUM-FR
VAL-IT
Gibberellin
Hungary
ALF-ES
FIN-GB
GLO-BE
GOB-IT
HRM-BE
NLI-AT
SUM-FR
Nicotine
United Kingdom
JAH-GB
PBC-ES
UPL-GB
Pyrethrins
Italy
ALF-ES
BRA-GB
CAP-FR
FBL-DE
MGK-GB
ORI-GB
PBC-ES
PBK-AT
PYC-FR
SAM-FR
SBS-IT
Rotenone
France
FBL-DE
IBT-IT
SAP-FR
SBS-IT
SFS-FR
Group 2.2.
LEAD RAPPORTEUR: UNITED KINGDOM
Active substance
Rapporteur Member State
Notifier
(A)
(B)
(C)
Citronellol
(see also Group 6.1)
United Kingdom
ACP-FR
Citrus extract Notified as Bactericide
United Kingdom
ALF-ES
Citrus extract/grapefruit extract
United Kingdom
Citrus extract/Grapefruit seed extract
Notified as Disinfectant
United Kingdom
BOB-DK
Conifer needle powder
Latvia
Garlic extract
Notified as repellant
Poland
ALF-ES-016
CRU-IT-005
ECY-GB-001
IAB-ES-001
PBC-ES-004
SBS-IT-003
SIP-IT-002
TRD-FR-001
VAL-IT-011
Garlic pulp
Poland
Extract from Equisetum
Latvia
Lecithin
Italy
DUS-DE
FBL-DE
PBC-ES
Marigold extract
Spain
ALF-ES
Mimosa Tenuiflora extract
Spain
ALF-ES
Mustard powder
Latvia
Pepper
Notified as repellant
United Kingdom
BOO-GB
PBI-GB
Plant oils/Black currant bud oil
Notified as repellant
Sweden
IAS-SE
Plant oils/Citronella oil
United Kingdom
BAR-GB
PBI-GB
Plant oils/Clove oil
Notified as repellant
United Kingdom
IAS-SE
XED-FR
Plant oils/Etheric oil (Eugenol)
Notified as repellant
Sweden
DEN-NL
DKI-NL
Plant oils/Eucalyptus oil
Sweden
CFP-FR
SIP-IT
Plant oils/Gaiac Wood oil
Spain
IAS-SE
Plant oils/Garlic oil
United Kingdom
DEN-NL
GSO-GB
Plant oils/Lemongrass oil
Notified as repellant
United Kingdom
IAS-SE
Plant oils/Marjoram oil
Notified as repellant
United Kingdom
DEN-NL
Plant oils/Olive oil
United Kingdom
DKI-NL
Plant oils/Orange oil
Notified as repellant
United Kingdom
GSO-GB
Plant oils/Pinus oil
Sweden
ACP-FR
DKI-NL
IBT-IT
MIB-NL
SPU-DE
Plant oils/Rape seed oil
Spain
CEL-DE
CRU-IT
DKI-NL
FBL-DE
NEU-DE
NOV-FR
PBI-GB
VIT-GB
Plant oils/Soya oil
Notified as repellant
Sweden
DEN-NL
DKI-NL
PBC-ES
Plant oils/Spear mint oil
Sweden
XED-FR
Plant oils/Sunflower oil
Spain
DKI-NL
PBI-GB
TRD-FR
Plant oils/Thyme oil
Notified as repellant
Sweden
DEN-NL
Plant oils/Ylang-Ylang oil
Notified as repellant
Sweden
IAS-SE
Quassia
Italy
AGE-IT
CAP-FR
FBL-DE
TRF-DE
ALF-ES
Sea-algae extract
Italy
ASU-DE
LGO-FR
OGT-IE
VAL-IT
Seaweed
Italy
ASF-IT
OGT-IE
VAL-IT
ALF-ES
ESA-NL
BAL-IE
AGC-FR
Extract from plant Red oak, Pronikly pear cactus, Fragrant sumac, Red mangrove
Poland
Extract from Menta piperata
Poland
Extract from tea tree
Latvia
GROUP 3
LEAD RAPPORTEUR: DENMARK
Active substance
Rapporteur Member State
Notifier
(A)
(B)
(C)
Chitosan
Denmark
ALF-ES
CLM-NL
IDB-ES
Gelatine
Denmark
MIB-NL
Hydrolysed proteins
(see also Group 6.2)
Greece
SIC-IT
GROUP 4
LEAD RAPPORTEUR: UNITED KINGDOM
Active substance
Rapporteur Member State
Notifier
(A)
(B)
(C)
1-Decanol
Italy
CRO-GB
OLE-BE
JSC-GB
Aluminium sulphate
Spain
FER-GB
GSO-GB
Calcium chloride
Spain
FBL-DE
Calcium hydroxide
Spain
PZD-NL
Carbon monoxide
United Kingdom
Carbon dioxide
Notified as insecticide/disinfectant
United Kingdom
FBL-DE
EDTA and salts thereof
Hungary
DKI-NL
Fatty alcohols/Aliphatic alcohols
Italy
JSC-GB
Iron sulphate
United Kingdom
BNG-IE
HTO-GB
KRO-DE
MEL-NL
Kieselgur (Diatomaceous earth)
Greece
ABP-DE
AGL-GB
AMU-DE
DKI-NL
FBL-DE
Lime sulphur (Calcium polysulphide)
Spain
FBL-DE
PLS-IT
STI-IT
Paraffin oil
Greece
FBL-DE
Paraffin oil/(CAS 64741-88-4)
Greece
BPO-GB
SUN-BE
Paraffin oil/(CAS 64741-89-5)
Greece
BPO-GB
PET-PT
SUN-BE
SUN-BE
XOM-FR
Paraffin oil/(CAS 64741-97-5)
Greece
BPO-GB
Paraffin oil/(CAS 64742-46-7)
Greece
TOT-FR
TOT-FR
TOT-FR
Paraffin oil/(CAS 64742-54-7)
Greece
CVX-BE
Paraffin oil/(CAS 64742-55-8/64742-54-7)
Greece
SAG-FR
Paraffin oil/(CAS 64742-55-8)
Greece
CPS-ES
CVX-BE
XOM-FR
Paraffin oil/(CAS 64742-65-0)
Greece
XOM-FR
Paraffin oil/(CAS 72623-86-0)
Greece
TOT-FR
Paraffin oil/(CAS 8012-95-1)
Greece
AVA-AT
Paraffin oil/(CAS 8042-47-5)
Greece
ASU-DE
ECP-DE
NEU-DE
Paraffin oil/(CAS 97862-82-3)
Greece
TOT-FR
TOT-FR
Petroleum oils
Spain
FBL-DE
Petroleum oils/(CAS 64742-55-8/64742-57-7)
Spain
GER-FR
Petroleum oils/(CAS 74869-22-0)
Spain
CVX-BE
RLE-ES
Petroleum oils/(CAS 92062-35-6)
Spain
RML-IT
Potassium permanganate
Spain
CNA-ES
FBL-DE
VAL-IT
Aluminium silicate (Kaolin)
Hungary
PPP-FR
Sodium aluminium silicate
Notified as repellant
Hungary
FLU-DE
Sulphur
France
ACI-BE
AGN-IT
BAS-DE
CER-FR
CPS-ES
FBL-DE
GOM-ES
HLA-GB
JCA-ES
NSC-GB
PET-PT
RAG-DE
RLE-ES
SAA-PT
SML-GB
STI-IT
SYN-GB
UPL-GB
ZOL-IT
Sulphuric acid
France
NSA-GB
Calcium carbonate
Spain
GROUP 5
LEAD RAPPORTEUR: SPAIN
Active substance
Rapporteur Member State
Notifier
(A)
(B)
(C)
2-Phenylphenol
Spain
BCH-DE
Ethanol
France
CGL-GB
Ethylene
United Kingdom
BRM-GB
COL-FR
GROUP 6
Group 6.1.
LEAD RAPPORTEUR: BELGIUM
Active substance
Rapporteur Member State
Notifier
(A)
(B)
(C)
Aluminium ammonium sulfate
Portugal
SPL-GB
Ammonium acetate
Portugal
LLC-AT
Anthraquinone
Belgium
TOM-FR
Bone oil
Notified as Repellant
Belgium
BRI-GB
FLU-DE
IOI-DE
ASU-DE
Calcium carbide
Portugal
CFW-DE
Citronellol
Notified as Repellant (see also Group 2.2)
United Kingdom
ASU-DE
CAL-FR
Denathonium benzoate
Portugal
ASU-DE
MFS-GB
Dodecyl alcohol
Portugal
SEI-NL
Lanolin
Slovak Republic
Methyl nonyl ketone
Belgium
PGM-GB
Polymer of styrene and acrylamide
Slovak Republic
Polyvinyl acetate
Slovak Republic
Repellants (by smell) of animal or plant origin/Blood meal
Belgium
GYL-SE
Repellants (by smell) of animal or plant origin/Essential oils
Belgium
BAR-GB
Trimethylamine hydrochloride
Belgium
LLC-AT
Repellant (by taste) of vegetal and animal origin/extract of food grade/phosphoric acid and fish flour
Belgium
2-hydroxyethyl butyl sulfide
Poland
Asphalts
Poland
Group 6.2.
LEAD RAPPORTEUR: GREECE
Active substance
Rapporteur Member State
Notifier
(A)
(B)
(C)
Ammonium bituminosulfonate
Hungary
Daphne oil
Slovenia
FLU-DE
Hydrolysed proteins
Notified as Attractant (see also Group 3.)
Greece
BIB-ES
PHY-GR
SIC-IT
Limestone — pulverized
Austria
Olein
Hungary
Quartz sand
Austria
ASU-DE
AVA-AT
DKI-NL
FLU-DE
Repellants (by smell) of animal or plant origin/Fatty acids, fish oil
Greece
ASU-DE
Repellants (by smell) of animal or plant origin/Fish oil
Greece
FLU-DE
Repellants (by smell) of animal or plant origin/Sheep fat
Greece
KWZ-AT
Repellants (by smell) of animal or plant origin/Tall oil (CAS 8016-81-7)
Greece
FLU-DE
Repellants (by smell) of animal or plant origin/Tall oil crude (CAS 93571-80-3)
Greece
ASU-DE
Repellants (by smell) of anímal or plant origin/tall oil
Greece
Urea
(see also Group 1)
Greece
PHY-GR
Chinin hydrochlorid
Hungary
PART B
LEAD RAPPORTEUR: AUSTRIA
RAPPORTEUR: AUSTRIA
(The Czech Republic, Poland and Italy shall be considered the rapporteur Member States in the sense of the obligation to cooperate with Austria in the evaluation, in accordance with the provisions of Article 16)
Active substance
Rapporteur Member State
Notifier
(A)
(B)
(C)
(2E,13Z)-Octadecadien-1-yl acetate
SEI-NL
SEI-NL
SEI-NL
(7E,9Z)-Dodecadienyl acetate
BAS-DE
CAL-FR
ISA-IT
LLC-AT
RUS-GB
SDQ-ES
SEI-NL
(7E,9Z)-Dodecadienyl acetate; (7E,9E)-Dodecadienyl acetate
SHC-FR
(7Z,11E)-Hexadecadien-1-yl acetate
SEI-NL
SEI-NL
(7Z,11Z)-Hexadecadien-1-yl acetate; (7Z,11E)-Hexadecadien-1-yl acetate
ABC-GB
LLC-AT
(9Z,12E)-Tetradecadien-1-yl acetate
RUS-GB
E)-11-Tetradecenyl acetate
SEI-NL
(E)-8-Dodecenyl acetate
CAL-FR
SEI-NL
(E,E)-8,10-Dodecadien-1-ol
BAS-DE
CAL-FR
ISA-IT
LLC-AT
RUS-GB
SDQ-ES
SEI-NL
SHC-FR
VIO-GR
MAS-BE
(E/Z)-8-Dodecenyl acetate; (Z)-8-Dodecenol
BAS-DE
CAL-FR
(E/Z)-9-Dodecenyl acetate; (E/Z)-9-Dodecen-1-ol; (Z)-11-Tetradecen-1-yl acetate
ISA-IT
LLC-AT
SDQ-ES
(E/Z)-9-Dodecenyl acetate; (E/Z)-9-Dodecen-1-ol; (Z)-11-Tetradecen-1-yl acetate
TRF-DE
(Z)-11-Hexadecen-1-ol
SEI-NL
(Z)-11-Hexadecen-1-yl acetate
SEI-NL
(Z)-11-Hexadecenal
SEI-NL
(Z)-11-Hexadecenal; (Z)-11-Hexadecen-1-yl acetate
LLC-AT
(Z)-11-Tetradecen-1-yl acetate
BAS-DE
SEI-NL
(Z)-13-Hexadecen-11-ynyl acetate
SDQ-ES
(Z)-13-Octadecenal
SEI-NL
(Z)-7-Tetradecenal
SEI-NL
(Z)-8-Dodecenol
SEI-NL
(Z)-8-Dodecenyl acetate
CAL-FR
SDQ-ES
SEI-NL
(Z)-8-Dodecenyl acetate; Dodecan-1-yl acetate
ISA-IT
(Z)-9-Dodecenyl acetate
BAS-DE
LLC-AT
SDQ-ES
SEI-NL
SHC-FR
(Z)-9-Dodecenyl acetate; Dodecan-1-yl acetate
ISA-IT
(Z)-9-Hexadecenal
SEI-NL
(Z)-9-Hexadecenal; (Z)-11-Hexadecenal; (Z)-13-Octadecenal
RUS-GB
SDQ-ES
(Z)-9-Tetradecenyl acetate
SEI-NL
(Z,E)-3,7,11-trimethyl-2,6,10-dodecatrien-1-ol (Farnesol)
CAL-FR
(Z,Z,Z,Z)-7,13,16,19-Docosatetraen-1-yl isobutyrate
SHC-FR
1,4-Diaminobutane (Putrescine)
Austria
LLC-AT
1,7-Dioxaspiro-5,5-undecan
VIO-GR
1-Tetradecanol
SEI-NL
2,6,6-Trimethylbicyclo[3.1.1]hept-2-ene(alpha-Pinen)
SHC-FR
3,7,7-Trimethylbicyclo[4.1.0]hept-3-ene (3-Carene)
3,7,11-Trimetil-1,6,10-dodecatrien-3-ol (Nerolidol)
CAL-FR
3,7 Dimethyl-26-octadien-1-ol (Geraniol)
CAL-FR
5-Decen-1-ol
BAS-DE
SEI-NL
5-Decen-1-yl acetate
BAS-DE
SEI-NL
5-Decen-1-yl acetate; 5-Decen-1-ol
LLC-AT
ISA-IT
(8E, 10E) – 8, 10 – Dodecadiene 1- yl acetate
Dodecan- 1 - yl acetate
(E) – 9- Dodecen – 1 – yl acetate
(E) – 8- Dodecen – 1 – yl acetate
2-Methyl-6-methylene-2,7-octadien-4-ol (ipsdienol)
4,6,6-Trimethyl-bicyclo[3.1.1]hept-3-en-ol,((S)-cis-verbenol)
2-Ethyl-1,6-dioxaspiro(4,4) nonan(chalcogran)
(IR)-1,3,3-Trimethyl-4,6-dioxatricyclo[3.3.1.02,7] nonane (lineatin)
(E,Z)-8,10-Tetradecadienyl
2-ethyl-1,6-Dioxaspiro (4,4) nonan
2-Methoxypropan-1-ol
2-Methoxypropan-2-ol
2-Methyl-3-buten-2-ol
(E)-2-Methyl-6-methylene-2,7-octadien-1-ol(myrcenol)
(E)-2-Methyl-6-methylene-3,7-octadien-2-ol(isomyrcenol)
2-Methyl-6-methylene-7-octen-4-ol (Ipsenol)
3-Methyl-3-buten-1-ol
Ethyl 2,4-decadienoate
Methyl p-hydroxybenzoate
p-Hydroxybenzoic acid
1-Methoxy-4-propenylbenzene (Anethole)
1-Methyl-4-isopropylidenecyclohex-1-ene (Terpinolene)
PART C
LEAD RAPPORTEURS: NETHERLANDS, SWEDEN
Active substance
Rapporteur Member State
Notifier
(A)
(B)
(C)
Agrobacterium radiobacter K 84
Denmark
Bacillus sphaericus
France
SUM-FR
Bacillus subtilis strain IBE 711
Germany
Bacillus thuringiensis aizawai
Italy
ISA-IT
MAS-BE
SIP-IT
SUM-FR
Bacillus thuringiensis israelensis
Italy
SIP-IT
SUM-FR
Bacillus thuringiensis kurstaki
Denmark
ALF-ES
ASU-DE
IAB-ES
MAS-BE
PRO-ES
SIP-IT
SUM-FR
IBT-IT
ISA-IT
Bacillus thuringiensis tenebrionis
Italy
SUM-FR
Baculovirus GV
Germany
Beauveria bassiana
Germany
AGI-IT
AGR-ES
CAL-FR
MEU-GB
Beauveria brongniartii
Germany
CAL-FR
Cydia pomonella granulosis virus
Germany
MAS-BE
CAL-FR
PKA-DE
SIP-IT
Metarhizium anisopliae
Netherlands
AGF-IT
IBT-IT
TAE-DE
Neodiprion sertifer nuclear polyhedrosis virus
Finland
VRA-FI
Phlebiopsis gigantea
Estonia
FOC-GB
VRA-FI
Pythium oligandrun
Sweden
Streptomyces griseoviridis
Estonia
VRA-FI
Trichoderma harzianum
Sweden
BBI-SE
IAB-ES
IBT-IT
ISA-IT
AGF-IT
BOB-DK
KBS-NL
Trichoderma polysporum
Sweden
BBI-SE
Trichoderma viride
France
AGB-IT
ISA-IT
Verticillium dahliae
Netherlands
ARC-NL
Verticillium lecanii
Netherlands
KBS-NL
PART D
LEAD RAPPORTEUR: GERMANY
Active substance
Rapporteur Member State
Notifier
(A)
(B)
(C)
Aluminium phosphide
Germany
CAT-PT
DET-DE
Brodifacum
Italy
PEL-GB
Bromadiolone
Sweden
ABB-GB
CAL-FR
LIP-FR
Chloralose
Portugal
PHS-FR
Chlorophacinone
Spain
CAL-FR
CFW-DE
FRU-DE
LIP-FR
Difenacoum
Finland
APT-GB
CAL-FR
SOX-GB
Magnesium phosphide
Germany
DET-DE
Tricalcium phosphate
Germany
CHM-FR
Zinc phosphide
Germany
CFW-DE
Carbon monoxide
Italy
PART E
Active substance
Rapporteur Member State
Notifier
(A)
(B)
(C)
Aluminium phosphide
Germany
DET-DE
UPL-GB
Magnesium phosphide
Germany
DET-DE
UPL-GB
PART F
LEAD RAPPORTEUR: NETHERLANDS
Active substance
Rapporteur Member State
Notifier
(A)
(B)
(C)
Didecyl-dimethylammonium chloride
Netherlands
LON-DE
Formaldehyde
Notified as Disinfectant
Netherlands
PSD-GB
Glutaraldehyde
Belgium
BAS-DE
HBTA (High Boiling Tar Acid)
Notified as Disinfectant
Ireland
JEY-GB
Hydrogen peroxide
Finland
FBL-DE
KIR-NL
SPU-DE
Peracetic acid
Netherlands
SOL-GB
Phoxim
Finland
BCS-DE
Sodium hypochlorite
Netherlands
SPU-DE
Sodium lauryl sulfate
Netherlands
ADC-DE
Sodium p-toluenesulphon-chloramide
Netherlands
PNP-NL
PART G
LEAD RAPPORTEUR: POLAND
Active substance
Rapporteur Member State
Notifier
(A)
(B)
(C)
2-Methoxy-5-nitrofenol sodium salt
Poland
3(3-Benzyloxycarbonyl-methyl)-2-benzothiazolinone (Benzolinone)
Slovak Republic
Cumylphenol
Poland
Fat destilation residues
Czech Republic
Flufenzin
Hungary
Flumetsulam
Slovak Republic
Ethanedial (glyoxal)
Poland
Hexamethylene tetramine (urotropin)
Slovak Republic
Lactofen
Czech Republic
Propisochlor
Hungary
2-Mercaptobenzothiazole
Poland
Biohumus
Poland
Di-1-p-menthene
Poland
Jasmonic acid
Hungary
N-phenylphthalamic acid
Hungary
Copper complex: 8-hydroxyquinolin with salicylic acid
Poland
1,3,5-Tir-(2-hydroxyethyl)-hexa-hydro-s-triazyne
Poland
(1) The active substances for which no notifier is identified in Column C are active substances as meant in Article 1(1)(b) of this Regulation.
ANNEX II
List of notifiers' code identification, names and addresses
Code identification
Name
Address
ABB-GB
Activa/Babolna Bromadiolone Task Force
8 Cabbage Moor
Great Shelford
Cambridge CB2 5NB
United Kingdom
Tel. (44-1223) 84 04 89
Fax (44-1223) 84 04 89
hancock@chemregservs.co.uk
ABC-GB
AgriSense-BCS Ltd
Treforest Industrial Estate
Pontypridd
Mid Glamorgan CF37 5SU
United Kingdom
Tel. (44-1443) 84 11 55
Fax (44-1443) 84 11 52
mail@agrisense.demon.co.uk
ABP-DE
Agrinova GmbH
Hauptstraße 13
D-67283 Obrigheim/Mühlheim
Tel.: (49) 6359 32 14
Fax: (49) 6359 32 14
agrinova@t-online.de
ACI-BE
Agriculture Chimie Industrie International
Avenue Albert 233
B-1190 Bruxelles
Téléphone (32-2) 508 10 93
Télécopieur (32-2) 514 06 32
roland.levy@swing.be
ACP-FR
Action Pin
ZI de Cazalieu
BP 30
F-40260 Castets des Landes
Téléphone (33) 558 55 07 00
Télécopieur (33) 558 55 07 07
actionpin@action-pin.fr
ADC-DE
ADC Agricultural Development Consulting
Am Vilser Holz 17
D-27305 Bruchhausen-Vilsen
Tel.: (49) 4252-27 81
Fax: (49) 4252-35 98
stratmannb@adc-eu.com
AGB-IT
Agribiotec srl
Via San Bernardo, 22
I-26100 Cremona
Tel. (39) 0535 467 02
Fax (39) 0535 591 95
paolo.lameri@agribiotec.com
AGC-FR
Agrimer
BP 29
Prat Menan
F-29880 Plouguerneau
Téléphone (33) 298 04 54 11
Télécopieur (33) 298 04 55 15
fnicolas@agrimer.com
AGE-IT
Agrivet S.a.s. di Martinelli Maurizio & C.
Via S. Giovanni, 6050
I-40024 Castel San Pietro (BO)
Tel. (39) 051 94 91 19
Fax (39) 051 615 31 85
r.martinelli@bo.nettuno.it
AGF-IT
Agrifutur srl
Agrifutur srl
Via Campagnole, 8
I-25020 Alfianello (Brescia)
Tel. (39) 030 993 47 76
Fax (39) 030 993 47 77
rkm@numerica.it
AGI-IT
Agrimix s.r.l.
Viale Città d'Europa 681
I-00144 Roma
Tel. (39) 06 529 62 21
Fax (39) 06 529 14 22
info@agrimix.com
AGL-GB
Agil Ltd
Hercules 2, Calleva Park
Aldermaston
Reading RG7 8DN
United Kingdom
Tel. (44-118) 981 33 33
Fax (44-118) 981 09 09
murray@agil.com
AGN-IT
Zolfindustria Srl
Via Cantarana, 17
I-27043 San Cipriano Po (PV)
Tel. (39) 0385 24 17 00
Fax (39) 0385 24 17 05
agrindustria.srl@tin.it
AGR-ES
Agrichem, SA
Plaza de Castilla, 3, 14A
E-28046 Madrid
Tel. (34) 913 14 98 88
Fax (34) 913 14 98 87
info@agrichembio.com
AIF-IT
Aifar Agricola SRL
Registration Department
Via Bazzano 12
I-16019 Ronco Scrivia (GE)
Tel. (39) 010 935 02 67
Fax (39) 010 935 05 32
posta@aifar.it
ALF-ES
Alfarin Química SA
Ibiza 35, 5oC
E-28009 Madrid
Tel. (34) 915 74 87 07
Fax (34) 915 04 31 59
alfarin@asertel.es
ALT-FR
Alltech France
EU Regulatory Affairs Department
2-4 avenue du 6 juin 1944
F-95190 Goussainville
Téléphone (33) 134 38 98 98
Télécopieur (33) 134 38 98 99
gbertin@alltech.com
AMI-IT
Aminco Srl
Via Mandilli 14
I-12071 Bagnasco (Cn)
Tel. (39) 0174 71 66 06
Fax (39) 0174 71 39 63
aminco@isiline.it
AMU-DE
Amu-Systeme
Büschem 13
D-53940 Hellenthal
Tel.: (49) 2482 10 24
Fax: (49) 2482 70 89
amu-hellenthal@t-online.de
AMV-GB
Amvac Chemical UK LTD
Surrey Technology Centre
40 Occam Rd
The Surrey Research Park
Guildford GU2 7YG
United Kingdom
Tel. (44-1483) 29 57 80
Fax (44-1483) 28 57 81
amvacat@easynet.co.uk
APT-GB
Activa/PelGar Brodifacoum and Difenacoum task Force
8 Cabbage Moor
Great Shelford
Cambridge CB2 5NB
United Kingdom
Tel. (44-1223) 84 04 89
Fax (44-1223) 84 04 89
hancock@chemregservs.co.uk
ARC-NL
Arcadis PlanRealisatie B.V.
Tree Services
Marowijne 80
NL-7333 PJ Apeldoorn
Tel.: (31-55) 599 94 44
Fax: (31-55) 533 88 44
r.valk@arcadis.nl
ASF-IT
Asfaleia SRL.
Via Mameli, 6
I-06124 Perugia
Tel. (39) 075 573 49 35
Fax (39) 017 82 25 26 32
postmaster@asfaleia.it
ASP-NL
Asepta B.V.
PO Box 33
Cyclotronweg 1
NL-2600 AA Delft
Tel.: (31-15) 256 92 10
Fax: (31-15) 257 19 01
a.vandenende@asepta.nl
ASU-DE
Stähler Agrochemie GmbH & Co. KG
Stader Elbstraße
D-21683 Stade
Tel.: (49) 4141 92 040
Fax: (49) 4141 92 0410
staehler-agro@staehler.com
AVA-AT
Avenarius-Agro GmbH
Industriestraße 51
A-4600 Wels
Tel.: (43) 7242-489-0
Fax: (43) 7242-489-5
d.stroh@avenarius-agro.at
BAR-GB
Barrier Biotech Limited
36 Haverscroft Ind. Est.
New Road
Attleborough Norfolk NR17 1YE
United Kingdom
Tel. (44-1953) 45 63 63
Fax (44-1953) 45 55 94
nigelb@barrier-biotech.com
BAS-DE
BASF Aktiengesellschaft
APT/EQM — V 005
D-67056 Ludwigshafen
Tel.: (49) 621 607 90 26
Fax: (49) 621 605 20 40
siegfried.kersten@basf-ag.de
BBI-SE
Binab Bio-Innovation AB
Florettgatan 5
S-254 67 Helsingborg
Tfn (46-42) 16 37 04
Fax (46-42) 16 24 97
info@binab.se
BCH-DE
Bayer/Dow Task Force via Bayer AG, Bayer Chemicals
D-51368 Leverkusen
Tel.: (49) 214 306 22 68
Fax: (49) 214 307 23 39
klaus.stroech.ks@bayerchemicals.com
BAL-IE
BioAtlantis Ltd
Baylands, Ballyard
Tralee
County Kerry
Ireland
Tel. (353-66) 71-28592
Fax (353-66) 711 98 02
jtostralee@eircom.net
BCP-GB
Biological Crop Protection Ltd
Occupation Road, Wye
Ashford TN25 5EN
United Kingdom
Tel. (44-1233) 81 32 40
Fax (44-1233) 81 33 83
richardc@biological-crop-protection.co.uk
BCS-DE
Bayer CropScience AG
Alfred-Nobel-Straße 50
D-40789 Monheim am Rhein
Tel.: (49) 2173 38 33 63
Fax: (49) 2173 38 49 27
norbert.hesse@bayercropscience.com
BCS-FR
Bayer CropScience SA
14-20 rue Pierre Baizet
BP 9163
F-69263 Lyon Cedex 09
Téléphone (33) 472 85 25 25
Télécopieur (33) 472 85 30 82
martyn.griffiths@bayercropscience.com
BIB-ES
Bioibérica, SA
Polígono Industrial Mas Puigvert
Ctra. N-II Km. 680,6
E-08389 Palafolls, Barcelona
Tel. (34) 937 65 03 90
Fax (34) 937 65 01 02
ibartoli@bioiberica.com
BNG-IE
Brown & Gillmer LTD.
Florence Lodge
199 Strand Road, Merrion
Dublin 4
Ireland
Tel. (353-1) 283 82 16
Fax (353-1) 269 58 62
bgfeeds@indigo.ie
BOB-DK
Borregaard BioPlant ApS
Helsingforsgade 27 B
DK-8200 Århus N
Tlf. (45) 86 78 69 88
Fax (45) 86 78 69 22
borregaard@bioplant.dk
BOO-GB
Bootman Chemical Safety Ltd.
Diss Business Centre
Diss IP21 4HD
United Kingdom
Tel. (44-1379) 64 05 34
Fax (44-1379) 64 08 35
info@bootmanchem.com
BPO-GB
BP Global Special Products Ltd
Witan Gate House
500-600 Witan Gate
Milton Keynes MK9 1ES
United Kingdom
Tel. (44-1908) 85 33 44
Fax (44-1908) 85 38 96
gspinfo@bp.com
BRA-GB
BRA-Europe
33 Khattoun Road
Tooting Broadway
London SW17 OJA
United Kingdom
Tel. (44-208) 378 05 17
Fax (44-208) 378 05 17
braeurope@aol.com
BRI-GB
Brimac Carbon Services
21 Dellingburn Street
Greenock PA15 4TP
United Kingdom
Tel. (44-1475) 72 02 73
Fax (44-1475) 72 00 16
info@brimacservices.com
BRM-GB
BRM Agencies
Cheshire House
164 Main Road
Goostrey CW4 8JP
United Kingdom
Tel. (44-1477) 54 40 52
Fax (44-1477) 53 71 70
brianmartin@cheshirehouse.co.uk
CAL-FR
Calliope SAS
Route d'Artix
BP 80
F-64150 Noguères
Téléphone (33) 559 60 92 92
Télécopieur (33) 559 60 92 19
fleconte@calliope-sa.com
CAP-FR
Capiscol
160 route de la Valentine
F-13011 Marseille
Téléphone (33) 491 24 45 45
Télécopieur (33) 491 24 46 11
anne.coutelle@capiscol.com
CAT-PT
Cafum
Centro Agro Técnico de Fumigações Lda.
Rua de Moçambique 159 A2
PT-3000 Coimbra
Tel.: (351-239) 40 10 60 ou (351-239) 40 59 70
Fax: (351-239) 70 43 76
cafum@cafum.pt
CEL-DE
Scotts Celaflor GmbH
Konrad-Adenauer-Straße 30
D-55218 Ingelheim
Tel.: (49) 6132 78 03-0
Fax: (49) 6132 20 67
otto.schweinsberg@scotts.com
CEQ-ES
Cequisa
Muntaner, 322, 1o
E-08021 Barcelona
Tel. (34) 932 40 29 10
Fax (34) 932 00 56 48
xavier@cequisa.com
CER-FR
Cerexagri SA
1 rue des Frères Lumière
F-78373 Plaisir
Téléphone (33) 130 81 73 00
Télecopieur (33) 130 81 72 50
mark.egsmose@cerexagri.com
CFP-FR
Nufarm SA
Département ‘Homologations et Règlementation’
28 boulevard Camélinat
F-92230 Gennevilliers
Téléphone (33) 140 85 50 20
Télecopieur (33) 140 85 51 56
claude.chelle@fr.nufarm.com
CFW-DE
Chemische Fabrik Wülfel GmbH & Co. KG
Hildesheimer Straße 305
D-30519 Hannover
Tel.: (49) 511 984 96-0
Fax: (49) 511 984 96-40
cfw@wuelfel.de
CGL-GB
Catalytic Generators UK Limited
Mariel T Monk
2 Priory Court Pilgrim Street
London
United Kingdom
Tel. (44-207) 236 14 14
Fax (44-207) 329 87 87
london@merricks.co.uk
CHE-DK
Cheminova A/S
Registration Department
P.O. Box 9
DK-7620 Lemvig
Tel. (45) 96 90 96 90
Fax (45) 96 90 96 91
info@cheminova.dk
CHM-FR
Chemimpex SA/Mauer
1817 Route de Tutegny
F-01170 Cessy
Téléphone (33) 450 41 48 60
amselian@aol.com
CLM-NL
CLM research and advice Plc
PO Box 10015
Amsterdamsestraatweg 877
NL-3505 AA Utrecht
Tel.: (31-30) 244 13 01
Fax: (31-30) 244 13 18
clm@clm.nl
CNA-ES
Carus Nalon SL
Barrio Nalon s/n
E-33100 Trubia/Oviedo
Tel. (34) 985 78 55 13
Fax (34) 985 78 55 10
carus@carusnalon.com
COL-FR
Coleacp
5 rue de la Corderie
CENTRA 342
F-94586 Rungis Cedex
Téléphone (33) 141 80 02 10
Télécopieur (33) 141 80 02 19
coleacp@coleacp.org
CPS-ES
Cepsa
Av. Partenón, 12
Campo de las Naciones
E-28042 Madrid
Tel. (34) 913 37 96 69
Fax (34) 913 37 96 09
aranzazu.guzman@madrid.cepsa.es
CRO-GB
Crompton Europe Limited
Kennet House
4 Langley Quay, Langley
Slough SL3 6EH
United Kingdom
Tel. (44-1753) 60 30 48
Fax (44-1753) 60 30 77
phil.pritchard@cromptoncorp.com
CRT-GB
Certis
1b Mills Way
Boscombe Bown Business Park
Amesbury SP4 7RX
United Kingdom
Tel. (44-1980) 67 65 00
Fax (44-1980) 62 65 55
certis@certiseurope.co.uk
CRU-IT
Cerrus sas
Via Papa Giovanni XXIII, 84
I-21040 Uboldo (VA)
Tel. (39) 02 96 78 21 08
Fax (39) 02 96 78 29 01
cerrus@tiscalinet.it
PZD-NL
Plantenziektenkundige Dienst
PO Box 9102
NL-6700 HC Wageningen
Tel.: (31-31) 749 69 11
Fax: (31-31) 742 17 01
p.jellema@pd.agro.nl
CVX-BE
ChevronTexaco Technology Ghent
Technologiepark — Zwijnaarde 2
B-9052 Gent/Zwijnaarde
Tel. (32) 9 240 71 11
Fax (32) 9 240 72 22
arickjl@chevrontexaco.com
DEN-NL
DeruNed bv
Marconistraat 10
NL-2665 JE Bleiswijk
Tel.: (31-10) 522 15 14
Fax: (31-10) 522 02 50
deruned@deruned.nl
DET-DE
Detia Freyberg GmbH
Dr.-Werner-Freyberg-Straße 11
D-69514 Laudenbach
Tel.: (49) 6201 708-0
Fax: (49) 6201 708-427
zulassung@detia-degesch.de
DKI-NL
Denka International B.V.
Hanzeweg 1
NL-3771 NG Barneveld
Tel.: (31-34) 245 54 55
Fax: (31-34) 249 05 87
info@denka.nl
DUS-DE
Degussa Texturant Systems Deutschland GmbH & Co. KG
Ausschläger Elbdeich 62
D-20539 Hamburg
Tel.: (49) 40 789 55-0
Fax: (49) 40 789 55 83 29
reception.hamburg@degussa.com
DXN-DK
Duxon ApS
Skovgaardsvænget 628
DK-8310 Tranbjerg J
Tlf. (45) 96 23 91 00
Fax (45) 96 23 91 02
duxon@mail.tele.dk
ECP-DE
Elefant Chemische Produkte GmbH
Ringstraße 35—37
D-70736 Fellbach
Tel.: (49) 711 58 00 33
Fax: (49) 711 58 00 35
elefant-gmbh@web.de
ECY-GB
ECOspray Ltd
Grange Farm
Cockley Cley Road
Hilborough Thetford
IP26 5BT
United Kingdom
Tel. (44-176) 75 61 00
Fax (44-176) 75 63 13
enquiries@ecospray.com
ERO-IT
Euroagro s.r.l.
via Lazzaretti 5/A
I-42100 Reggio Emilia
Tel. (39) 0522 51 86 86
Fax (39) 0522 51 49 91
euroagro_italia@libero.it
ESA-NL
ECOstyle BV
Vaart Noordzijde 2a
NL-8426 AN Appelscha
Tel.: (31-51) 643 21 22
Fax: (31-51) 643 31 13
info@ecostyle.nl
ESS-IT
Esseco SpA
Via San Cassiano 99
I-28069 Trecate (Novara)
Tel. (39) 0321 790-1
Fax (39) 0321 790-215
chemsupport@esseco.it
FBL-DE
FiBL Berlin e.V.
Dr. K. Wilbois
Rungestraße 29
D-10179 Berlin
Tel.: (49) 6257 50 54 89
Fax: (49) 6257 50 54 98
klaus-peter.wilbois@fibl.de
FER-GB
Feralco (UK) Limited
Ditton Road
Widnes WA8 0PH
United Kingdom
Tel. (44-151) 802 29 10
Fax (44-151) 802 29 99
barry.lilley@feralco.com
FIN-GB
Fine Agrochemicals Ltd
Hill End House
Whittington
Worcester WR5 2RQ
United Kingdom
Tel. (44-1905) 36 18 00
Fax (44-1905) 36 18 10
enquire@fine-agrochemicals.com
FLU-DE
Flügel GmbH
Westerhöfer Straße 45
D-37520 Osterode/Harz
Tel.: (49) 5522 823 60
Fax: (49) 5522 843 26
info@fluegel-gmbh.de
FOC-GB
Forestry Commission
Forestry Commission Silvan House
231 Corstorphine Road
Edinburgh EH12 7AT
United Kingdom
Tel. (44-131) 334 03 03
Fax (44-131) 334 30 47
james.dewar@forestry.gsi.gov.uk
FRB-BE
Mr. John Ivey
Les Clos des Coulerins
F-74580 Viry
Téléphone (33) 450 04 76 01
Télécopieur (33) 450 04 76 01
JIvey94819@aol.com
FRU-DE
Frunol Delizia GmbH
Dübener Straße 145
D-04509 Delitzsch
Tel.: (49) 34202 65 30-0
Fax: (49) 34202 65 30-9
info@frunol-delicia.de
GER-FR
Germicopa SAS
1 allée Loeiz-Herrieu
F-29334 Quimper Cedex
Téléphone (33) 298 10 01 00
Télécopieur (33) 298 10 01 42
jeanyves.abgrall@germicopa.fr
GLO-BE
Globachem NV
Leeuwerweg 138
B-3803 Sint-Truiden
Tel. (32-1) 178 57 17
Fax (32-1) 168 15 65
globachem@globachem.com
GOB-IT
L. Gobbi s.r.l.
Registration Department
Via Vallecalda 33
I-16013 Campo Ligure (GE)
Tel. (39) 010 92 03 95
Fax (39) 010 92 14 00
info@lgobbi.it
GOM-ES
Gomensoro Química SA
Torneros, 14
Polígono Industrial Los Ángeles
E-28906 Getafe, Madrid
Tel. (34) 916 95 24 00
Fax (34) 916 82 36 99
gomenki@arrakis.es
GSO-GB
Growing Success Organics Limited
Hill Top Business Park
Devizes Road
Salisbury SP3 4UF
United Kingdom
Tel. (44-1722) 33 77 44
Fax (44-1722) 33 31 77
info@growingsucess.org.uk
GTL-GB
Growth Technology Ltd
Unit 66, Taunton Trading Estate
Taunton TA2 6RX
United Kingdom
Tel. (44-1823) 32 52 91
Fax (44-1823) 32 54 87
info@growthtechnology.com
GYL-SE
Gyllebo Gödning AB
Vessmantorpsvägen 16
S-260 70 Ljungbyhed
Tfn (46-435) 44 10 40
Fax (46-435) 44 10 40
gyllebo.plantskydd@telia.com
HAS-GR
House of Agriculture Spirou Aebe
Dr Dinos Chassapis, Assistant
Professor in Chemistry
5, Markoni Str.
GR-122 42 Athens
Τηλ.: (30) 210-349 75 00
Φαξ: (30) 210-342 85 01
agrospir@spirou.gr
HLA-GB
Headland Agrochemicals Ltd
Norfolk House
Great Chesterford CB10 1PF
United Kingdom
Tel. (44-1799) 53 01 46
Fax (44-1799) 53 02 29
stephen.foote@headlandgroup.com
HOC-GB
Hockley International Limited
Hockley House
354 Park Lane
Poynton Stockport SK12 1RL
United Kingdom
Tel. (44-1625) 87 85 90
Fax (44-1625) 87 72 85
mail@hockley.co.uk
HRM-BE
Hermoo Belgium NV
Zepperenweg 257
B-3800 Sint-Truiden
Tel. (32-1) 168 68 66
Fax (32-1) 170 74 84
hermoo@hermoo.be
HTO-GB
Tioxide Europe Ltd
Haverton Hill Road
Billingham TS23 1PS
United Kingdom
Tel. (44-1642) 37 03 00
Fax (44-1642) 37 02 90
greg_s_mcnulty@huntsman.com
IAB-ES
IAB, SL (Investigaciones y Aplicaciones Biotecnológicas, SL)
Ctra. Moncada-Náquera, km 1,7
E-46113 Moncada (Valencia)
Tel. (34) 961 30 90 24
Fax (34) 961 30 92 42
iab@iabiotec.com
IAS-SE
Interagro Skog AB
Eliselund
S-247 92 Södra Sandby
Tfn (46-46) 532 00
Fax (46-46) 532 08
walde@interagroskog.se
IBT-IT
Intrachem Bio Italia Spa
Via XXV Aprile 44
I-24050 Grassobbio Bergamo
Tel. (39) 035 33 53 13
Fax (39) 035 33 53 34
info@intrachem.it
IDB-ES
Idebio SL
Bell, 3 — Polígono El Montalvo
E-37188 Carbajosa De La Sagrada
Salamanca
Tel. (34) 92 31 92 40
Fax (34) 92 31 92 39
idebio@helcom.es
IOI-DE
Imperial-Oel-Import Handelsgesellschaft mbH
Bergstraße 11
D-20095 Hamburg
Tel.: (49) 4033 85 33-0
Fax: (49) 4033 85 33 85
info@imperial-oel-import.de
ISA-IT
Isagro S.p.A.
Via Caldera 21
20153 Milano
Tel. (39) 0240 90 11
Fax (39) 0240 90 12 87
agiambelli@isagro.it
JAH-GB
J A Humphrey Agriculture
189 Castleroe Road
Coleraine BT51 3QT
United Kingdom
Tel. (44-28) 70 86 87 33
Fax (44-28) 70 86 87 35
rhumphrey@nicobrand.com
JCA-ES
Julio Cabrero y Cía, SL
Puerto De Requejada
E-39312-Requejada (Cantabria)
Tel. (34) 942 82 40 89
Fax (34) 942 82 50 57
julio.cabrero@juliocabrero.com
JEY-GB
Jeyes Ltd
Brunel Way
Thetford IP24 1HF
United Kingdom
Tel. (44-1842) 75 45 67
Fax (44-1842) 75 76 83
nigel.cooper@jeyes.co.uk
JSC-GB
JSC International Ltd
Osborne House
20 Victoria Avenue
Harrogate HG1 5QY
United Kingdom
Tel. (44-1423) 52 02 45
Fax (44-1423) 52 02 97
terry.tooby@jsci.co.uk
KBS-NL
Koppert Beheer BV
Department R&D Microbials and Regulatory Affairs
Veilingweg 17/PO Box 155
NL-2650 AD Berkel en Rodenrijs
Tel.: (31-10) 514 04 44
Fax: (31-10) 511 52 03
info@koppert.nl
KIR-NL
Kemira Chemicals B.V.
PO Box 1015
NL-3180 AA Rozenburg
Tel.: (31-18) 128 25 40
Fax: (31-18) 128 25 36
dees_van.kruyssen@kemira.com
KRO-DE
Kronos International, INC.
Peschstraße 5
D-51373 Leverkusen
Tel.: (49) 214 356-0
Fax: (49) 214 421 50
kronos.leverkusen@nli-usa.com
KWZ-AT
F. Joh. Kwizda GmbH
Sarea Saatguttechnik
Freilingerstraße 44
A-4614 Marchtrenk
Tel.: (43) 7243 535 26-0
Fax: (43) 7243 535 26-12
office@sarea.at
LGO-FR
Laboratoires GOËMAR SA
ZAC La Madeleine
Avenue Général-Patton
F-35400 Saint-Malo
Téléphone (33) 299 21 53 70
Télécopieur (33) 299 82 56 17
labo@goemar.com
LIP-FR
LiphaTech SA
201 rue Carnot
F-94126 Fontenay-sous-Bois
Téléphone (33) 143 94 55 50
Télécopieur (33) 148 77 44 31
ahoussin@merck.fr
LLC-AT
Consep GmbH
Furth 27
A-2013 Gollersdorf
Tel.: (43) 2954 30244
Fax: (43) 2954 30245
wmaxwald@lander.es
LON-DE
Lonza GmbH
Morianstraße 32
D-42103 Wuppertal
Tel.: (49) 202 245 38 33
Fax: (49) 202 245 38 30
gisbert.mehring@lonzagroup.com
LUX-NL
Luxan B.V.
Industrieweg 2
NL-6662 PA Elst
Tel.: (31-48) 136 08 11
Fax: (31-48) 137 67 34
luxan@luxan.nl
MAK-BE
Makhteshim-Agan International Coordination Centre (MAICC)
Avenue Louise 283
B-1050 Bruxelles
Téléphone (32-2) 646 86 06
Télécopieur (32-2) 646 91 52
steve.kozlen@maicc.be
MAS-BE
Mitsui AgriScience International SA/BV
Boulevard de la Woluwe 60
Woluwedal 60
B-1200 Brussel
Tel.: (32-2) 331 38 94
Fax: (31-2) 331 38 60
thorez@certiseurope.fr
MEL-NL
Melchemie Holland B.V.
Postbus 143
NL-6800 AC Arnhem
Tel.: (31-26) 445 12 51
Fax: (31-26) 442 50 93
info@melchemie.com
MEU-GB
Mycotech Europe LTD.
12 Lonsdale Gardens
Tunbridge Wells TN1 1PA
United Kingdom
Tel. (44-1580) 88 20 59
Fax (44-1580) 88 20 57
fjr@agrilexuk.com
MFS-GB
Macfarlan Smith Limited
Wheatfield Road
Edinburgh EH11 2QA
United Kingdom
Tel. (44-131) 337 24 34
Fax (44-131) 337 98 13
melanie.jackson@macsmith.com
MGK-GB
MGK Europe Limited
21 Wilson Street
London EC2M 2TD
United Kingdom
Tel. (44-207) 588 08 00
Fax (44-207) 588 05 55
glazer.barry@dorseylaw.com
MIB-NL
Micro Biomentor BV
PO Box 50
Middelbroekweg 67
2675 ZH Honselersdijk
Tel.: (31-17) 462 67 63
Fax: (31-17) 461 40 76
info@microbiomentor.nl
NDC-SE
NIM Distribution Center AB
Stigbergsvägen 4
S-141 32 Huddinge
Tfn (46-8) 740 26 30
Fax (46-8) 740 2618
info@bionim.com
NEU-DE
W. Neudorff GmbH KG
An der Mühle 3
D-31860 Emmerthal
Tel.: (49) 5155 624-126
Fax: (49) 5155 60 10
wilhelmy@neudorff.de
NLI-AT
Nufarm GmbH & Co KG
Registration Department
St.-Peter-Straße 25
A-4021 Linz
Tel.: (43) 732 69 18-0
Fax: (43) 732 69 18-2004
eric.gibert@at.nufarm.com
NOV-FR
Novance SA
Venette
BP 20609
F-60206 Compiègne
Téléphone (33) 344 90 70 96
Télécopieur (33) 344 90 70 70
p.ravier@novance.com
NSA-GB
National Sulphuric Acid Association Limited
19 Newgate Street
Chester CH1 1DE
United Kingdom
Tel. (44-1244) 32 22 00
Fax (44-1244) 34 51 55
tomfleet@nsaa.org.uk or pamlatham@nsaa.org.uk
NSC-GB
Novigen Sciences Ltd
2D Hornbeam Park Oval
Harrogate HG2 8RB
United Kingdom
Tel. (44-1423) 85 32 00
Fax (44-1423) 81 04 31
charris@novigensci.co.uk
OGT-IE
Oilean Glas Teoranta
Meenmore
Dungloe
County Donegal
Ireland
Tel. (353-75) 213 19
Fax (353-75) 218 07
smgo11@gofree.indigo.ie
OLE-BE
Oleon nv
Assenedestraat 2
B-9940 Ertvelde
Tel.: (32-9) 341 10 11
Fax: (32-9) 341 10 00
info@oleon.com
OMX-GB
Omex Agriculture Ltd
Bardney Airfield
Tupholme
Lincoln LN3 5TP
United Kingdom
Tel. (44-1526) 39 60 00
Fax (44-1526) 39 60 01
enquire@omex.com
ORI-GB
Organic Insecticides
Parkwood, Maltmans Lane
Gerrards Cross SL9 8RB
United Kingdom
Tel. (44-1494) 81 65 75
Fax (44-1494) 81 65 78
OSK-ES
Osku España, SL
Polígono Industrial El Zurdo, nave 13
Ctra. de la Estación
E-Abarán, Murcia
Tel. (34) 968 77 06 23
Fax (34) 968 77 06 12
oskuesp@oskuesp.e.telefonica.net
PAB-SE
Perstorp Specialty Chemicals AB
S-284 80 Perstorp
Tfn (46-435) 380 00
Fax (46-435) 381 00
perstorp@perstorp.com
PBC-ES
Procesos Bioquímicos Claramunt-Forner, SL
Senda de les Deu, 11
E-46138 Rafelbunol, Valencia
Tel. (34) 961 40 21 69
Fax (34) 961 40 21 69
ana.perez@acgbioconsulting.com
PBI-GB
pbi Home & Garden Ltd
Durhan House
214-224 High Street
Waltham Cross EN8 7DP
United Kingdom
Tel. (44-1992) 78 42 00
Fax (44-1992) 78 49 50
teresa.jones@pbi.co.uk
PBK-AT
Manfred Pfersich, Kenya Pyrethrum Information Centre
Kenya Pyrethrum Information Centre
Haslaustraße 807
A-5411 Oberalm
Tel.: (43) 6245 83 38 10
Fax: (43) 6245 823 56
manfred.pfersich@kenya-pyrethrum.com
PEL-GB
PelGar International Ltd.
Index House, Peak Centre
Midhurst Rd
Liphook GU30 7TN
United Kingdom
Tel. (44-1428) 72 22 50
Fax (44-1428) 72 28 11
info@pelgar.demon.co.uk
PET-PT
Petrogal, S.A.
Rua Tomás da Fonseca, Torre C
PT-1600-209 Lisboa
Tel.: (351-21) 724 26 08
Fax: (351-21) 724 29 53
luis.brito.soares@galpenergia.com
PGM-GB
Pet and Garden Manufacturing plc
Queens Rd.
Sanquhar DG4 6DN
United Kingdom
Tel. (44-1223) 84 04 89
Fax (44-1223) 84 04 89
hancock@chemregservs.co.uk
PHS-FR
Physalys
3 rue de l'Arrivée — BP 215
F-75749 Paris Cedex 15
Téléphone (33) 143 21 70 62
Télécopieur (33) 143 21 70 63
ybassat@physalys.com
PHY-GR
Phytophyl N·G· Stavrakis
Averof 16
GR-104 33 Athens
Τηλ.: (30) 22620 586 70
Φαξ: (30) 22620 587 35
nista@otenet.gr
PKA-DE
Probis GmbH & Andermatt Biocontrol Taskforce
Daimlerstraße 16/1
D-75446 Wiernheim
Tel.: (49) 7044 91 42 21
Fax: (49) 7044 91 42 25
probis.knoch@t-online.de
PLS-IT
Polisenio srl.
Via S. Andrea 10
I-48022 Lugo (RA)
Tel. (39) 0545 245 60
Fax (39) 0545 245 87
polisenio@lamiarete.com
PNP-NL
PNP Holding bv
Nijverheidsplein 21 G
NL-3771 MR Barneveld
Tel.: (31-34) 240 47 60
Fax: (31-34) 240 47 67
info@axcentive.com
PPP-FR
Plant Protection Projects
Le Pont Neuf
Route de Gordes
F-84220 Cabriéres d'Avignon
Téléphone (33) 432 52 17 51
Télécopieur (33) 490 76 80 71
stephen.shires@wanadoo.fr
PRO-ES
Probelte, SA
Ctra. Madrid, km. 384,6 Polígono Industrial
El Tiro
E-30100 Espinardo (Murcia)
Tel. (34) 968 30 72 50
Fax (34) 968 30 54 32
probelte@probelte.es
PSD-GB
Pesticides Safety Directorate
Mallard House, Kings Pool
3 Peasholme Green
York YO1 7PX
United Kingdom
Tel. (44-1904) 64 05 00
Fax (44-1904) 45 57 33
Information@psd.defra.gsi.gov.uk
PUN-DK
Punya Innovations
Almevej 180
DK-3250 Gilleleje
Tlf (45) 48 30 17 27
Fax (45) 48 30 22 27
punya@worldonline.dk
PYC-FR
Pyco SA
Route de Saint-Sever — Haut-Mauco
BP 27
F-40001 Mont-de-Marsan Cedex
Téléphone (33) 558 05 89 37
Télécopieur (33) 558 05 89 36
alain.dini@bayercropscience.com
RAG-DE
agrostulln GmbH
Werksweg 2
D-92551 Stulln
Tel.: (49) 9435 39 32 27
Fax: (49) 9435 39 32 28
m.meier@agrostulln.de
RHZ-NL
Rhizopon B.V.
PO Box 110
NL-2394 ZG Hazerswoude
Tel.: (31-71) 341 51 46
Fax: (31-71) 341 58 29
info@rhizopon.com
RLE-ES
Repsolypf Lubricantes y Especialidades
Orense, 34
E-28020 Madrid
Tel. (34) 913 48 78 00
Fax (34) 913 23 70 32
msalinasg@repsolypf.com
RML-IT
R.A.M.OIL S.p.A.
Via Filichito 16/A
Tavernanova di Casalnuovo
I-80013 Napoli
Tel. (39) 081 519 51 11
Fax (39) 081 842 10 79
info@ramoil.it
RUS-GB
Russell Fine Chemicals Ltd
68 Third Avenue
Deeside Industrial Park
Deeside CH5 2LA
United Kingdom
Tel. (44-1244) 28 13 33
Fax (44-1244) 28 18 78
alzaidi@Russellipm.com
SAA-PT
Sapec Agro, S.A.
Rua Victor Cordon, 19
PT-1200-482 Lisboa
Tel.: (351-21) 322 27 49
Fax: (351-21) 322 27 35
cesmeraldo@agro.sapec.pt
SAG-FR
JP Industrie
16 avenue des Chateaupieds
F-92565 Rueil-Malmaison
Téléphone (33) 155 47 96 60
Télécopieur (33) 155 47 96 69
service.client@jp-industrie.com
SAM-FR
Samabiol SA
La Grande Marine
F-84800 Isle-sur-la-Sorgue
Téléphone (33) 490 21 44 44
Télécopieur (33) 490 38 10 55
samabiol@samabiol.com
SAP-FR
Saphyr
ZI des Terriers
F-06600 Antibes
Téléphone (33) 493 74 73 13
Télécopieur (33) 493 74 82 30
saphyr@rotenone.com
SBS-IT
Serbios S.r.l.
VIA E.FERMI, 112
I-45021 Badia Polesine (RO)
Tel. (39) 0425 59 06 22
Fax (39) 0425 59 08 76
info@serbios.it
SDQ-ES
Sociedad Española de Desarrollos Químicos, SA (SEDQ)
Avenida Diagonal, 352, entresuelo
E-08013 Barcelona
Tel. (34) 934 58 40 00
Fax (34) 934 58 40 07
jcastella@sedq.es
SEI-NL
Shin-Etsu International Europe B V
World Trade Center Amsterdam
Strawinskylaan B-827
NL-1077 XX Amsterdam
Tel.: (31-20) 662 13 59
Fax: (31-20) 664 90 00
shinint@attglobal.net
SFS-FR
Scotts France SAS
21 chemin de la Sauvegarde
BP 92
F-69136 Écully Cedex
Téléphone (33) 472 86 67 00
Télécopieur (33) 472 86 67 86
nicolas.le-brun-keris@scottsco.com
SHC-FR
SiberHegner & Cie. (France) S.A.
1475 quai du Rhône — BP 266
F-01702 Miribel Cedex
Téléphone (33) 478 55 78 73
Télécopieur (33) 478 55 78 87
thomas.steinmann@SiberHegner.com
SIC-IT
SICIT 2000 S.p.A.
Via Arzignano 80
I-36072 Chiampo (VI)
Tel. (39) 0444 62 31 32
Fax (39) 0444 62 59 03
sicitspa@tin.it
SIP-IT
Sipcam SpA
Via Sempione 195
I-20016 Pero (Milano)
Tel. (39) 02 35 37 84 00
Fax (39) 02 339 02 75
sipcam@sipcam.it
SLY-FR
Solvay SA
12 cours Albert 1er
F-75383 Paris cedex 08
Téléphone (33) 140 75 80 00
Télécopieur (33) 142 89 12 57
frederik.degraeve@Solvay.com
SML-GB
M/s Sulphur Mills Limited
C/o Unity Garments Ltd
Unity House, Fletcher Street
Bolton BL36 N3
United Kingdom
Tel. (44-1204) 49 73 78
Fax (44-1204) 49 73 78
sml@sulphurmills.com
SOL-GB
Solvay Interox Ltd
PO Box 7
Warrington WA4 6HB
United Kingdom
Tel. (44-1925) 64 35 12
Fax (44-1925) 65 58 56
tom.candy@solvay.com
SOX-GB
Sorex Limited
St Michael's Industrial Estate
Widnes WA8 8TJ
United Kingdom
Tel. (44-151) 420-7151
Fax (44-151) 495-1163
rogers@sorex.com
SPL-GB
Sphere Laboratories (London) Ltd
The Yews
Main Street
Chilton OX11 0RZ
United Kingdom
Tel. (44-1235) 83 18 02
Fax (44-1235) 83 38 96
bobn@jrfint.demon.co.uk
SPU-DE
Spiess-Urania Chemicals GmbH
Heidenkampsweg 77
D-20097 Hamburg
Tel.: (49) 4023 65 20
Fax: (49) 4023 65 22 80
mail@spiess-urania.com
STG-GB
Stephenson Group Limited
PO Box 305
Listerhills Road
Bradford BD7 1HY
United Kingdom
Tel. (44-1274) 72 38 11
Fax (44-1274) 37 01 08
ssc@stephensongroup.co.uk
STI-IT
S.T.I. — Solfotecnica Italiana S.p.A.
Via Evangelista Torricelli, 2
I-48010 Cotignola (RA)
Tel. (39) 0545 99 24 55
Fax (39) 0545 90 82 87
aamenta@solfotecnica.com
SUM-FR
Valent BioSciences
Parc d'affaires de Crécy
2 rue Claude-Chappe
F-69370 Saint-Didier-au-Mont-d'Or
Téléphone (33) 478 64 32 60
Télécopieur (33) 478 47 70 05
denise.munday@valentbiosciences.ch
SUN-BE
Sun Oil Company Belgium NV
Ingberthoeveweg 4
B-2630 Aartselaar
Tel.: (32-3) 458 12 30
Fax: (31-3) 458 14 78
info@sunoco.be
SYN-GB
Syngenta
European Regional Centre
Surrey Research Park, Priestley Road
Guildford GU2 7YH
United Kingdom
Tel. (44-1483) 26 02 40
Fax (44-1483) 26 00 19
simon.baker@syngenta.com
TAE-DE
Earth BioScience, Inc. (formerly Taensa, Inc.)
c/o Bayer AG
Agricultural Centre Monheim
D-51368 Leverkusen
dhd@dhd-consulting.de
TBE-ES
Tratamientos Bio-Ecológicos, SA
Polígono Industrial Los Urreas, 31
E-30730 San Javier (Murcia)
Tel. (34) 968 57 20 04
Fax (34) 968 19 22 51
trabe1@telefonica.net
TEM-DE
Temmen GmbH
Ankerstraße 74
D-65795 Hattersheim
Tel.: (49) 6145 99 19-0
Fax: (49) 6145 99 19-19
temmen@aol.com
TOM-FR
Arysta Paris SAS
18 avenue de l'Opéra
F-75001 Paris
Téléphone (33) 142 96 14 56
Télécopieur (33) 142 97 52 91
oudar@par.tomen.co.uk
TOT-FR
Total Solvants
51 esplanade du Général-de-Gaulle
La Défense 10
F-92069 Paris-La Défense
Téléphone (33) 141 35 59 83
Télécopieur (33) 141 35 51 34
christian.varescon@totalfinaelf.com
TRD-FR
La Toulousaine de Recherche et de Développement
Zone industrielle de Pompignal
F-31190 Miremont
Téléphone (33) 561 50 61 58
Télécopieur (33) 561 50 84 42
anne.paulhe@latoulousaine.fr
TRF-DE
Trifolio-M GmbH
Sonnenstraße 22
D-35633 Lahnau
Tel.: (49) 6441 631 14
Fax: (49) 6441 646 50
info@trifolio-m.de
UPL-GB
United Phosphorus Ltd
Chadwick House
Birchwood Park
Warrington XWA3 6AE
United Kingdom
Tel. (44-1925) 85 90 09
Fax (44-1925) 85 19 51
julie@uplukreg.demon.co.uk
VAL-IT
Valagro S.p.A.
Zona Industriale
I-66040 Piazzano di Atessa — Chieti
Tel. (39) 0872 88 11
Fax (39) 0872 88 13 95
o.larocca@valagro.com
VIO-GR
Vioryl S.A.
36 Viltaniotis St.
Kato Kifissia
GR-145 64 Athens
Τηλ.: (30) 210-807 46 03
Φαξ: (30) 210-807 46 81
vioryl@vioryl.gr
VIT-GB
Vitax Ltd
Owen Street
Coalville LE67 3DE
United Kingdom
Tel. (44-530) 51 00 60
Fax (44-530) 51 02 99
tech@vitax.co.uk
VRA-FI
Verdera Oy
P.O. Box 330
Porkkalankatu 3
FI-00101 Helsinki
Tel. (358) 10 86 15 11
Fax (358) 108 62 11 26
maiju.heith@kemira.com
XED-FR
Xeda International SA
2 ZA de la Crau
F-13670 Saint-Andiol
Téléphone (33) 490 90 23 23
Télécopieur (33) 490 90 23 20
xeda.int@wanadoo.fr
XOM-FR
ExxonMobil
2 rue des Martinets
F-92500 Rueil-Malmaison
Téléphone (33) 147 10 60 00
Télécopieur (33) 147 10 66 03
olivier.traversaz@exxonmobil.com
ZOL-IT
Zolfital SpA
Via di S. Teresa 23
I-00198 Roma RM
Tel. (39) 06 854 10 96
Fax (39) 06 854 31 49
zolfital@tin.it
ANNEX III
Co-ordinating authority in the Member States (more details are available at the following webside: http://www.europa.eu.int/comm/food/fs/ph_ps/pro/index_en.htm)
AUSTRIA
Bundesamt für Ernährungssicherheit
Landwirtschaftliche Untersuchungen und Forschung Wien
Spargelfeldstraße 191
A-1220 Wien
BELGIUM
Service public fédéral Santé publique, Sécurité de la Chaîne alimentaire et Alimentation
Direction-générale Animaux, Végétaux et Alimentation
Centre administratif de l'État, bâtiment Arcades
B-1010 Bruxelles
CYPRUS
Ministry of Agriculture,
Natural resources and Environment
Department of Agriculture
Loukis Akritas Ave.
1412 Lefkosia
CZECH REPUBLIC
State Phytosanitary Administration,
PPP Division
Zemědělská 1A
61300 Brno
DENMARK
Ministry of Environment and Energy
Danish Environmental Protection Agency
Pesticide Division
Strandgade 29
DK-1401 Copenhagen K
ESTONIA
Estonian Plant Production Inspectorate
Plant Protection Department
Teaduse 2
75501 Saku
Harju Country
Estonia
FINLAND
Plant Production Inspection Centre
Pesticide Division
P.O. BOX 42
FI-00501 Helsinki
FRANCE
Ministère de l’agriculture, de l’alimentation, de la pêche et des affaires rurales
Sous direction de la qualité et de la protection des végétaux
Bureau de la réglementation et de la mise sur le marché des intrans
251, rue de Vaugirard
F-75732 Paris Cedex 15
GERMANY
Bundesamt für Verbraucherschutz und Lebensmittelsicherheit (BVL)
Abteilung 2, Pflanzenschutzmittel
Dienststelle Braunschweig
Messeweg 11—12
D-38104 Braunschweig
GREECE
Hellenic Republic
Ministry of Agriculture
General Directorate of Plant Produce
Directorate of Plant Produce Protection
Department of Pesticides
3-4 Hippokratous Street
GR-10164 Athens
HUNGARY
Central Service for Plant Protection and Soil conservation
Budaörsi út 141–145.
1118 Budapest
IRELAND
Pesticide Control Service
Department of Agriculture and Food
Abbotstown Laboratory Complex
Abbotstown, Castleknock
IRL-Dublin 15
ITALY
Ministero della Salute
Direzione Generale della Sanità Pubblica Veterinaria, degli Alimenti e della Nutrizione
Piazza G. Marconi, 25
I-00144 Roma
LATVIA
State Plant Protection Service
Plant Protection Department
Republikas laukums 2,
Riga, LV-1981
Latvia
LITHUANIA
State Plant Protection Service
Kalvarijų 62
09304 Vilnius
Lithuania
LUXEMBOURG
Administration des Services Techniques de l’Agriculture
Service de la protection des Végétaux
Boîte postale 1904
16, route d’Esch
L-1019 Luxembourg
MALTA
Ministry for rural Affairs & The Environment
Plant Health Department
Plant Biotechnology Centre
Annibale Preca Street
NETHERLANDS
College voor de Toelating van Bestrijdingsmiddelen
PO Box 217
NL-6700 AE Wageningen
POLAND
Ministerstwo Rolnictwa i Rozwoju Wsi
Departament Hodowli i Ochrony Roślin
ul. Wspólna 30
00-930 Warszawa
PORTUGAL
Direcção-Geral de Protecção das Culturas,
Quinta do Marquês
P-2780 Oeiras
SLOVAK REPUBLIC
Ministry of Agriculture of the Slovak Republic,
Plant Commodities Department
Dobrovičova 12
81266 Bratislava
SLOVENIA
Ministry of Agriculture, Forestry and Food,
Phytosanitary Administration Republic of Slovenia
6 Einspielerjeva,
SI-1000 Ljubljana
SPAIN
Ministerio de Agricultura, Pesca y Alimentación
Dirección General de Agricultura
Subdirección General de Medios de Producción Agrícolas
Avda. Alfonso XII, 62
E-28014 Madrid
SWEDEN
The Swedish Chemicals Inspectorate, KemI
P.O. Box 2
SE-172 13 Sundbyberg
UNITED KINGDOM
Pesticides Safety Directorate
Department for Environment, Food and Rural Affairs
Mallard House,
Kings Pool,
3 Peasholme Green,
York, YO1 7PX
ANNEX IV
Organisations in the Member States to be contacted concerning further details on the payment of the fees referred to in Article 30 and to which such fees have to be paid
AUSTRIA
Bundesamt für Ernährungssicherheit
Landwirtschaftliche Untersuchungen und Forschung Wien
Spargelfeldstraße 191
A-1220 Wien
BELGIUM
Fonds budgétaire des matières premières et des produits
Service public fédéral Santé publique, Sécurité de la Chaîne alimentaire et Alimentation
Direction-générale Animaux, Végétaux et Alimentation
Centre administratif de l'État, bâtiment Arcades
B-1010 Bruxelles
CYPRUS
Ministry of Agriculture,
Natural resources and Environment
Department of Agriculture
Loukis Akritas Ave.
1412 Lefkosia
CZECH REPUBLIC
State Phytosanitary Administration,
PPP Division
Zemědělská 1A
61300 Brno
DENMARK
Ministry of Environment and Energy
Danish Environmental Protection Agency
Strandgade 29
DK-1401 Copenhagen K
ESTONIA
Estonian Plant Production Inspectorate
Plant Protection Department
Teaduse 2
75501 Saku
Harju Country
Estonia
FINLAND
Plant Production Inspection Centre
Pesticide Division
PO BOX 42
FI-00501 Helsinki
Bank and account:
Nordea Bank
Account: 166030-101330
IBAN: FI3716603000101330
SWIFT: NDEAFIHH
FI-00501 Helsinki
FRANCE
Ministère de l’Agriculture et de la Pêche
Bureau de la Réglementation des Produits antiparasitaires — 251 rue de Vaugirard
F-75732 Paris Cedex 15
GERMANY
Bundesamt für Verbraucherschutz und Lebensmittelsicherheit (BVL)
Abteilung 2, Pflanzenschutzmittel
Dienststelle Braunschweig
Messeweg 11—12
D-38104 Braunschweig
GREECE
Hellenic Republic
Ministry of Agriculture
General Directorate of Plant Produce
Directorate of Plant Produce Protection
Department of Pesticides
3-4 Hippokratous Street
GR-10164 Athens
HUNGARY
Central Service for Plant Protection and Soil conservation
Budaörsi út 141–145.
1118 Budapest
IRELAND
Pesticide Control Service
Department of Agriculture, Food and Rural Development
Abbotstown Laboratory Complex
Abbotstown, Castleknock
IRL-Dublin 15
ITALY
Tesoreria Provinciale dello Stato di Viterbo
N. di conto corrente postale n. 52744570
IBAN: IT 43
CIN: E
BIC: BPPIITRRXXX
ABI: 7601
CAB: 14500
LATVIA
State Plant Protection Service
Plant Protection Department
Republikas laukums 2,
Riga, LV-1981
Latvia
LITHUANIA
State Plant Protection Service
Kalvarijų 62
09304 Vilnius
Lithuania
LUXEMBOURG
Administration des Services Techniques de l’Agriculture
Boîte postale 1904
L-1019 Luxembourg
MALTA
Ministry for rural Affairs & The Environment
Plant Health Department
Plant Biotechnology Centre
Annibale Preca Street
THE NETHERLANDS
College voor de Toelating van Bestrijdingsmiddelen
PO Box 217
NL-6700 AE Wageningen
POLAND
Ministerstwo Rolnictwa i Rozwoju Wsi
Departament Hodowli i Ochrony Roślin
ul. Wspólna 30
00-930 Warszawa
PORTUGAL
Direcção-Geral de Protecção das Culturas,
Quinta do Marquês,
P-2780 OEIRAS
Número de conta: 003505840003800793097
Banco: Caixa Geral de Depósitos
SLOVAK REPUBLIC
Ministry of Agriculture of the Slovak Republic,
Plant Commodities Department
Dobrovičova 12
81266 Bratislava
SLOVENIA
Ministry of Agriculture, Forestry and Food,
Phytosanitary Administration Republic of Slovenia
6 Einspielerjeva,
SI-1000 Ljubljana
SPAIN
Ministerio de Agricultura, Pesca y Alimentación
Dirección General de Agricultura
Subdirección General de Medios de Producción Agrícolas
Avda. Alfonso XII, 62
E-28014 Madrid
SWEDEN
The Swedish Chemicals Inspectorate, KemI
P.O. Box 2
SE-172 13 Sundbyberg
National Giro Account: 4465054 – 7
UNITED KINGDOM
Pesticides Safety Directorate
Department for Environment, Food and Rural Affairs
Mallard House,
Kings Pool,
3 Peasholme Green,
York, YO1 7PX
ANNEX V
Details to be notified by producers in new Member States
The notification must be made on paper and by e-mail.
The notification shall contain the following information:
1.
IDENTIFICATION DATA ON THE NOTIFIER
1.1.
Manufacturer of the active substance as defined in point (b) of Article 2 of Regulation (EC) No 1112/2002 (name, address, including location of plant):
1.2.
Name and address of the producer as defined in point (a) of Article 2 of Regulation (EC) No 1112/2002 including the name of the (natural) person responsible for the notification and further engagements resulting from this Regulation.
1.2.1.
(a)
Telephone No
(b)
Telefax No
(c)
E-Mail Address
1.2.2.
(a)
Contact:
(b)
Alternative:
2.
INFORMATION TO FACILITATE IDENTIFICATION
2.1.
Common name (proposed or ISO-accepted where appropriate) specifying, where relevant, any variants thereof such as salts, esters or amines produced by the manufacturer. For micro-organisms the species, and where relevant, subspecies name
2.2.
Chemical name (IUPAC and CAS nomenclature) (where appropriate).
2.3.
CAS, CIPAC and EEC numbers (if available).
2.4.
Empirical and structural formula, molecular mass (where appropriate).
2.5.
Any other information considered necessary to facilitate identification, for example method of manufacture/extraction or origin of materials from which the substance is manufactured.
2.6.
Specification of purity of the active substance in g/kg or g/l (as appropriate).
3.
FURTHER INFORMATION
3.1.
For each Member State a list of crops/uses for which plant protection products containing the active substance are currently authorised or used.
4.
UNDERTAKING
The notifier undertakes to submit to the designated coordinating authority of the designated rapporteur Member State the dossiers within the time limits provided for in Article 12 of Regulation (EC) No 2229/2004.
The notifier declares that he is aware that he will be charged a fee by Member States at the time of the submission of the full dossier.
The notifier confirms that the above information is honest and correct.
The notifier declares that an authorisation by the manufacturer to act as his sole representative for the purpose of complying with this Regulation is enclosed if necessary.
Signature (of the person competent to act for the manufacturer mentioned under 1.1.)