COM(2008)9 - Safety of toys

Please note

This page contains a limited version of this dossier in the EU Monitor.

Contents

  1. Key information
  2. Key dates
  3. Related information
  4. Resulting legislation
  5. Full version
  6. EU Monitor

1.

Key information

official title

Proposal for a Directive of the European Parliament and of the Council on the safety of toys
 
Legal instrument Directive
Decision making procedure ordinary legislative procedure (COD)
reference by COM-number143 COM(2008)9 EN
Additional COM-numbers SEC(2008)38; SEC(2008)39
procedure number145 2008/0018(COD)
CELEX number146 52008PC0009

2.

Key dates

Document 25-01-2008
Online publication 25-01-2008
Decision 18-06-2009; Richtlijn 2009/48
Publication in Official Journal147 30-06-2009; OJ L 170, 30.6.2009,Special edition in Croatian: Chapter 13 Volume 055

3.

Related information

4.

Resulting legislation

 

5.

Full version

This page is also available in a full version containing the latest state of affairs, the summary of the European Parliament Legislative Observatory, the legal basis, the legal context, other dossiers related to the dossier at hand, the stakeholders involved (e.g. European Commission directorates-general, European Parliament committees, Council configurations and even individual EU Commissioners and Members of the European Parliament), consultations relevant to the dossier at hand and finally documents of the European Parliament, the Council of Ministers and the European Commission.

The full version is available for registered users of the EU Monitor by ANP and PDC Informatie Architectuur.

6.

EU Monitor

The EU Monitor enables its users to keep track of the European process of lawmaking, focusing on the relevant dossiers. It automatically signals developments in your chosen topics of interest. Apologies to unregistered users, we can no longer add new users.This service will discontinue in the near future.

  • 1. 
    OJ L 187, 16.7.1988, p.1.

     
  • 2. 
    COM/2003/0071 final.

     
  • 3. 
    Council Directive 93/68/EEC of 22 July 1993, OJ L 220, 30.8.1993, p.1.

     
  • 4. 
    Proposal for a Regulation on accreditation and market surveillance; COM(2007)37 final of 14/02/2007. Proposal for a Decision on a common framework for the marketing of goods; COM (2007) 53 final of 14/02/2007.

     
  • 5. 
    Substances CMR substances are categorised into categories 1, 2 and 3 based on the degree of evidence of their carcinogenic, mutagenic or reprotoxic properties. Category 1:
     
  • 6. 
    Commission Communication COM (2000) 1, 1.2.2000.

     
  • 7. 
    See footnote 4.

     
  • 8. 
    COM/2003/0071 final.

     
  • 9. 
    OJ C
     
  • 10. 
    OJ C
     
  • 11. 
    OJ C
     
  • 12. 
    OJ C
     
  • 13. 
    OJ L 187, 16.7.1988, p. 1. Directive as amended by Directive 93/68/EEC (OJ L 220, 30.8.1993, p. 1).

     
  • 14. 
    OJ L 204, 21,7.1998, p. 37.

     
  • 15. 
    OJ L 11, 15.1.2002, p. 4.

     
  • 16. 
    OJ L
     
  • 17. 
    OJ L 396, 30.12.2006, p. 1. Regulation as amended by Council Regulation (EC) No 1354/2007 (OJ L 304, 22.11.2007, p. 1).

     
  • 18. 
    OJ 196, 16.8.1967, p. 1. Directive as last amended by Directive 2006/121/EC of the European Parliament and of the Council (OJ L 396, 30.12.2006. p. 850).

     
  • 19. 
    OJ L 114, 27.4.2006, p. 9.

     
  • 20. 
    OJ L 37, 13.2.2003, p. 19.

     
  • 21. 
    OJ L 37, 13.2..2003, p. 24.

     
  • 22. 
    OJ L 365, 31.12.1994, p. 10.

     
  • 23. 
    OJ L 266, 26.9.2006, p. 1.

     
  • 24. 
    OJ L184, 17.7.1999, p. 23. Decision as amended by Decision 2006/512/EC (OJ L200, 22/7/2006, p.11).

     
  • 25. 
    OJ L
     
  • 26. 
    OJ L 187, 16.7.1988, p.1.

     
  • 27. 
    OJ L 187, 16.7.1988, p.1.

     
  • 28. 
    Substances CMR substances are categorised into categories 1, 2 and 3 based on the degree of evidence of their carcinogenic, mutagenic or reprotoxic properties. Category 1:
     
  • 29. 
    Commission Communication COM (2000) 1, 1.2.2000.

     
  • 30. 
    Substances CMR substances are categorised into categories 1, 2 and 3 based on the degree of evidence of their carcinogenic, mutagenic or reprotoxic properties. Category 1:
     
  • 31. 
    Commission Communication COM (2000) 1, 1.2.2000.

     
  • 32. 
    Council Directive 93/68/EEC of 22 July 1993, OJ L 220, 30.8.1993, p.1.

     
  • 33. 
    COM/2003/0071 final.

     
  • 34. 
    COM/2003/0071 final.

     
  • 35. 
    Substances CMR substances are categorised into categories 1, 2 and 3 based on the degree of evidence of their carcinogenic, mutagenic or reprotoxic properties. Category 1:
     
  • 36. 
    COM/2003/0071 final.

     
  • 37. 
    Proposal for a Regulation on accreditation and market surveillance; COM(2007)37 final of 14/02/2007. Proposal for a Decision on a common framework for the marketing of goods; COM (2007) 53 final of 14/02/2007.

     
  • 38. 
    Proposal for a Regulation on accreditation and market surveillance; COM(2007)37 final of 14/02/2007. Proposal for a Decision on a common framework for the marketing of goods; COM (2007) 53 final of 14/02/2007.

     
  • 39. 
    OJ L 187, 16.7.1988, p.1.

     
  • 40. 
    Council Directive 93/68/EEC of 22 July 1993, OJ L 220, 30.8.1993, p.1.

     
  • 41. 
    Proposal for a Regulation on accreditation and market surveillance; COM(2007)37 final of 14/02/2007. Proposal for a Decision on a common framework for the marketing of goods; COM (2007) 53 final of 14/02/2007.

     
  • 42. 
    Proposal for a Regulation on accreditation and market surveillance; COM(2007)37 final of 14/02/2007. Proposal for a Decision on a common framework for the marketing of goods; COM (2007) 53 final of 14/02/2007.

     
  • 43. 
    Proposal for a Regulation on accreditation and market surveillance; COM(2007)37 final of 14/02/2007. Proposal for a Decision on a common framework for the marketing of goods; COM (2007) 53 final of 14/02/2007.

     
  • 44. 
    Substances CMR substances are categorised into categories 1, 2 and 3 based on the degree of evidence of their carcinogenic, mutagenic or reprotoxic properties. Category 1:
     
  • 45. 
    COM/2003/0071 final.

     
  • 46. 
    COM/2003/0071 final.

     
  • 47. 
    OJ L 187, 16.7.1988, p.1.

     
  • 48. 
    Proposal for a Regulation on accreditation and market surveillance; COM(2007)37 final of 14/02/2007. Proposal for a Decision on a common framework for the marketing of goods; COM (2007) 53 final of 14/02/2007.

     
  • 49. 
    COM/2003/0071 final.

     
  • 50. 
    COM/2003/0071 final.

     
  • 51. 
    COM/2003/0071 final.

     
  • 52. 
    OJ No L 200, 30.7. 1999, p. 1-68

     
  • 53. 
    COM/2003/0071 final.

     
  • 54. 
    COM/2003/0071 final.

     
  • 55. 
    COM/2003/0071 final.

     
  • 56. 
    COM/2003/0071 final.

     
  • 57. 
    COM/2003/0071 final.

     
  • 58. 
    COM/2003/0071 final.

     
  • 59. 
    Council Directive 93/68/EEC of 22 July 1993, OJ L 220, 30.8.1993, p.1.

     
  • 60. 
    OJ L 187, 16.7.1988, p.1.

     
  • 61. 
    Substances CMR substances are categorised into categories 1, 2 and 3 based on the degree of evidence of their carcinogenic, mutagenic or reprotoxic properties. Category 1:
     
  • 62. 
    Differentiated appropriations

     
  • 63. 
    Non-differentiated appropriations hereafter referred to as NDA

     
  • 64. 
    Expenditure that does not fall under Chapter xx 01 of the Title xx concerned.

     
  • 65. 
    Expenditure within article xx 01 04 of Title xx.

     
  • 66. 
    Expenditure within chapter xx 01 other than articles xx 01 04 or xx 01 05.

     
  • 67. 
    See points 19 and 24 of the Interinstitutional agreement.

     
  • 68. 
    Cost of which is NOT covered by the reference amount

     
  • 69. 
    Cost of which is NOT covered by the reference amount

     
  • 70. 
    Cost of which is included within the reference amount

     
  • 71. 
    Specify the type of committee and the group to which it belongs.

     
  • 72. 
    OJ L 187, 16.7.1988, p.1.

     
  • 73. 
    COM/2003/0071 final.

     
  • 74. 
    Council Directive 93/68/EEC of 22 July 1993, OJ L 220, 30.8.1993, p.1.

     
  • 75. 
    Proposal for a Regulation on accreditation and market surveillance; COM(2007)37 final of 14/02/2007. Proposal for a Decision on a common framework for the marketing of goods; COM (2007) 53 final of 14/02/2007.

     
  • 76. 
    Substances CMR substances are categorised into categories 1, 2 and 3 based on the degree of evidence of their carcinogenic, mutagenic or reprotoxic properties. Category 1:
     
  • 77. 
    Commission Communication COM (2000) 1, 1.2.2000.

     
  • 78. 
    See footnote 4.

     
  • 79. 
    COM/2003/0071 final.

     
  • 80. 
    OJ C
     
  • 81. 
    OJ C
     
  • 82. 
    OJ C
     
  • 83. 
    OJ C
     
  • 84. 
    OJ L 187, 16.7.1988, p. 1. Directive as amended by Directive 93/68/EEC (OJ L 220, 30.8.1993, p.

    1).

     
  • 85. 
    OJ L 204, 21,7.1998, p. 37.

     
  • 86. 
    OJ L 11, 15.1.2002, p. 4.

     
  • 87. 
    OJ L
     
  • 88. 
    OJ L 396, 30.12.2006, p. 1. Regulation as amended by Council Regulation (EC) No 1354/2007 (OJ L 304, 22.11.2007, p.

    1).

     
  • 89. 
    OJ 196, 16.8.1967, p. 1. Directive as last amended by Directive 2006/121/EC of the European Parliament and of the Council (OJ L 396, 30.12.2006. p. 850).

     
  • 90. 
    OJ L 114, 27.4.2006, p. 9.

     
  • 91. 
    OJ L 37, 13.2.2003, p. 19.

     
  • 92. 
    OJ L 37, 13.2..2003, p. 24.

     
  • 93. 
    OJ L 365, 31.12.1994, p. 10.

     
  • 94. 
    OJ L 266, 26.9.2006, p. 1.

     
  • 95. 
    OJ L184, 17.7.1999, p. 23. Decision as amended by Decision 2006/512/EC (OJ L200, 22/7/2006, p.11).

     
  • 96. 
    OJ L
     
  • 97. 
    OJ L 187, 16.7.1988, p.1.

     
  • 98. 
    OJ L 187, 16.7.1988, p.1.

     
  • 99. 
    Substances CMR substances are categorised into categories 1, 2 and 3 based on the degree of evidence of their carcinogenic, mutagenic or reprotoxic properties. Category 1:
     
  • 100. 
    Commission Communication COM (2000) 1, 1.2.2000.

     
  • 101. 
    Substances CMR substances are categorised into categories 1, 2 and 3 based on the degree of evidence of their carcinogenic, mutagenic or reprotoxic properties. Category 1:
     
  • 102. 
    Commission Communication COM (2000) 1, 1.2.2000.

     
  • 103. 
    Council Directive 93/68/EEC of 22 July 1993, OJ L 220, 30.8.1993, p.1.

     
  • 104. 
    COM/2003/0071 final.

     
  • 105. 
    COM/2003/0071 final.

     
  • 106. 
    Substances CMR substances are categorised into categories 1, 2 and 3 based on the degree of evidence of their carcinogenic, mutagenic or reprotoxic properties. Category 1:
     
  • 107. 
    COM/2003/0071 final.

     
  • 108. 
    Proposal for a Regulation on accreditation and market surveillance; COM(2007)37 final of 14/02/2007. Proposal for a Decision on a common framework for the marketing of goods; COM (2007) 53 final of 14/02/2007.

     
  • 109. 
    Proposal for a Regulation on accreditation and market surveillance; COM(2007)37 final of 14/02/2007. Proposal for a Decision on a common framework for the marketing of goods; COM (2007) 53 final of 14/02/2007.

     
  • 110. 
    OJ L 187, 16.7.1988, p.1.

     
  • 111. 
    Council Directive 93/68/EEC of 22 July 1993, OJ L 220, 30.8.1993, p.1.

     
  • 112. 
    Proposal for a Regulation on accreditation and market surveillance; COM(2007)37 final of 14/02/2007. Proposal for a Decision on a common framework for the marketing of goods; COM (2007) 53 final of 14/02/2007.

     
  • 113. 
    Proposal for a Regulation on accreditation and market surveillance; COM(2007)37 final of 14/02/2007. Proposal for a Decision on a common framework for the marketing of goods; COM (2007) 53 final of 14/02/2007.

     
  • 114. 
    Proposal for a Regulation on accreditation and market surveillance; COM(2007)37 final of 14/02/2007. Proposal for a Decision on a common framework for the marketing of goods; COM (2007) 53 final of 14/02/2007.

     
  • 115. 
    Substances CMR substances are categorised into categories 1, 2 and 3 based on the degree of evidence of their carcinogenic, mutagenic or reprotoxic properties. Category 1:
     
  • 116. 
    COM/2003/0071 final.

     
  • 117. 
    COM/2003/0071 final.

     
  • 118. 
    OJ L 187, 16.7.1988, p.1.

     
  • 119. 
    Proposal for a Regulation on accreditation and market surveillance; COM(2007)37 final of 14/02/2007. Proposal for a Decision on a common framework for the marketing of goods; COM (2007) 53 final of 14/02/2007.

     
  • 120. 
    COM/2003/0071 final.

     
  • 121. 
    COM/2003/0071 final.

     
  • 122. 
    COM/2003/0071 final.

     
  • 123. 
    OJ No L 200, 30.7. 1999, p. 1-68

     
  • 124. 
    COM/2003/0071 final.

     
  • 125. 
    COM/2003/0071 final.

     
  • 126. 
    COM/2003/0071 final.

     
  • 127. 
    COM/2003/0071 final.

     
  • 128. 
    COM/2003/0071 final.

     
  • 129. 
    COM/2003/0071 final.

     
  • 130. 
    Council Directive 93/68/EEC of 22 July 1993, OJ L 220, 30.8.1993, p.1.

     
  • 131. 
    OJ L 187, 16.7.1988, p.1.

     
  • 132. 
    Substances CMR substances are categorised into categories 1, 2 and 3 based on the degree of evidence of their carcinogenic, mutagenic or reprotoxic properties. Category 1:
     
  • 133. 
    Differentiated appropriations

     
  • 134. 
    Non-differentiated appropriations hereafter referred to as NDA

     
  • 135. 
    Expenditure that does not fall under Chapter xx 01 of the Title xx concerned.

     
  • 136. 
    Expenditure within article xx 01 04 of Title xx.

     
  • 137. 
    Expenditure within chapter xx 01 other than articles xx 01 04 or xx 01 05.

     
  • 138. 
    See points 19 and 24 of the Interinstitutional agreement.

     
  • 139. 
    Cost of which is NOT covered by the reference amount

     
  • 140. 
    Cost of which is NOT covered by the reference amount

     
  • 141. 
    Cost of which is included within the reference amount

     
  • 142. 
    Specify the type of committee and the group to which it
     
  • 143. 
    De Europese Commissie kent nummers toe aan officiële documenten van de Europese Unie. De Commissie maakt onderscheid in een aantal typen documenten door middel van het toekennen van verschillende nummerseries. Het onderscheid is gebaseerd op het soort document en/of de instelling van de Unie van wie het document afkomstig is.
     
  • 144. 
    De Raad van de Europese Unie kent aan wetgevingsdossiers een uniek toe. Dit nummer bestaat uit een vijfcijferig volgnummer gevolgd door een schuine streep met de laatste twee cijfers van het jaartal, bijvoorbeeld 12345/00 - een document met nummer 12345 uit het jaar 2000.
     
  • 145. 
    Het interinstitutionele nummer is een nummerreeks die binnen de Europese Unie toegekend wordt aan voorstellen voor regelgeving van de Europese Commissie.
    Binnen de Europese Unie worden nog een aantal andere nummerseries gebruikt. Iedere instelling heeft één of meerdere sets documenten met ieder een eigen nummering. Die reeksen komen niet overeen met elkaar of het interinstitutioneel nummer.
     
  • 146. 
    Deze databank van de Europese Unie biedt de mogelijkheid de actuele werkzaamheden (workflow) van de Europese instellingen (Europees Parlement, Raad, ESC, Comité van de Regio's, Europese Centrale Bank, Hof van Justitie enz.) te volgen. EURlex volgt alle voorstellen (zoals wetgevende en begrotingsdossiers) en mededelingen van de Commissie, vanaf het moment dat ze aan de Raad of het Europees Parlement worden voorgelegd.
     
  • 147. 
    Als dag van bekendmaking van een Europees besluit geldt de dag waarop het besluit in het Publicatieblad wordt bekendgemaakt, en daardoor in alle officiële talen van de Europese Unie bij het Publicatiebureau beschikbaar is.
     
  • 148. 
    This legally binding act of the European Union establishes a set of objectives which all member states of the European Union must fulfil. The member states are required to implement directives. The member states are free to choose the manner they see fit to fulfil the required objectives.