Chwilio Deddfwriaeth

Commission Regulation (EC) No 2032/2003 (repealed)Dangos y teitl llawn

Commission Regulation (EC) No 2032/2003 of 4 November 2003 on the second phase of the 10-year work programme referred to in Article 16(2) of Directive 98/8/EC of the European Parliament and of the Council concerning the placing of biocidal products on the market, and amending Regulation (EC) No 1896/2000 (Text with EEA relevance) (repealed)

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  1. Introductory Text

  2. Article 1.Subject matter

  3. Article 2.Definitions

  4. Article 3.Existing Active Substances

  5. Article 4.Non-inclusion

  6. Article 4a.Essential use

  7. Article 4b.Extension of deadline for placing on the market

  8. Article 5.Review of notified existing active substances

  9. Article 6.Preparation of the complete dossier

  10. Article 7.Submission of the complete dossier

  11. Article 8.Joining, replacing or withdrawal of participants

  12. Article 9.Completeness check of dossiers

  13. Article 10.Evaluation of dossiers by the Rapporteur Member State

  14. Article 11.Commission procedures

  15. Article 12.. . . . . . . . . ....

  16. Article 13.Suspension of procedures

  17. Article 14.Amendments to Regulation (EC) No 1896/2000

  18. Article 15.Entry into force

  19. Signature

    1. ANNEX I

      EXISTING ACTIVE SUBSTANCES

      1. . . . . . . . . . ....

    2. ANNEX II

      EXISTING ACTIVE SUBSTANCES AND PRODUCT TYPES INCLUDED IN THE REVIEW PROGRAMME

      1. . . . . . . . . . ....

    3. ANNEX III

      EXISTING ACTIVE SUBSTANCES THAT HAVE BEEN IDENTIFIED BUT IN RESPECT OF WHICH NO NOTIFICATION HAS BEEN ACCEPTED OR NO MEMBER STATE HAS INDICATED AN INTEREST AND EXISTING ACTIVE SUBSTANCES THAT HAD BEEN NOTIFIED BUT IN RESPECT OF WHICH NO DOSSIER WAS SUBMITTED OR ACCEPTED AS COMPLETE AND FOR WHICH NO PRODUCER, FORMULATOR, ASSOCIATION, OTHER PERSON OR MEMBER STATE HAS INDICATED AN INTEREST TO TAKE OVER THE ROLE OF PARTICIPANT

      1. . . . . . . . . . ....

    4. ANNEX IV

      REQUIREMENTS FOR THE COMPLETE DOSSIER AND THE SUMMARY DOSSIER

      1. (a) . . . . . . . . . ....

      2. (b) The summary dossier must include the following:

      3. (c) . . . . . . . . . ....

      4. (d) . . . . . . . . . ....

    5. ANNEX V

      TIME PERIODS AND RAPPORTEUR MEMBER STATES FOR THE SUBMISSION OF COMPLETE DOSSIERS FOR EXISTING ACTIVE SUBSTANCES INCLUDED IN THE REVIEW PROGRAMME

      1. Part A

      2. Part B

      3. Part C

      4. Part D

    6. ANNEX VI

      COMPETENT AUTHORITIES, AS REFERRED TO IN ARTICLE 5(4) AS OF 1 MARCH 2005

      1. BELGIUM

      2. CZECH REPUBLIC

      3. DENMARK

      4. GERMANY

      5. ESTONIA

      6. GREECE

      7. SPAIN

      8. FRANCE

      9. IRELAND

      10. ITALY

      11. CYPRUS

      12. LATVIA

      13. LITUANIA

      14. LUXEMBOURG

      15. HUNGARY

      16. MALTA

      17. NETHERLANDS

      18. AUSTRIA

      19. POLAND

      20. PORTUGAL

      21. SLOVENIA

      22. SLOVAKIA

      23. FINLAND

      24. SWEDEN

      25. UNITED KINGDOM

      26. ICELAND

      27. NORWAY

    7. ANNEX VII

      EXISTING ACTIVE SUBSTANCES THAT WERE NOT IDENTIFIED BY 28 MARCH 2002 BUT MAY REMAIN ON THE MARKET UNTIL 1 SEPTEMBER 2006

      1. . . . . . . . . . ....

    8. ANNEX VIII

      EXISTING ACTIVE SUBSTANCES THAT WERE NOTIFIED BUT IN RESPECT OF WHICH NO DOSSIER WAS SUBMITTED OR ACCEPTED AS COMPLETE AND FOR WHICH ANOTHER PRODUCER, FORMULATOR, ASSOCIATION, OTHER PERSON OR MEMBER STATE HAS INDICATED AN INTEREST TO TAKE OVER THE ROLE OF PARTICIPANT

      1. . . . . . . . . . ....

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