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Commission Implementing Decision (EU) 2016/770 of 14 April 2016 establishing a common format for the submission of information concerning the operation of the procedures pursuant to Regulation (EU) No 649/2012 of the European Parliament and of the Council concerning the export and import of hazardous chemicals (notified under document C(2016) 2068)

EU Decision 2016/770 · Adopted 14 April 2016 · Extends to United Kingdom

Original text. legislation.gov.uk does not revise this item, so later amendments are not shown here. Changes made to it are listed under each provision when known.

Commission Implementing Decision (EU) 2016/770

of 14 April 2016

establishing a common format for the submission of information concerning the operation of the procedures pursuant to Regulation (EU) No 649/2012 of the European Parliament and of the Council concerning the export and import of hazardous chemicals

(notified under document C(2016) 2068)

THE EUROPEAN COMMISSION,

Having regard to the Treaty on the Functioning of the European Union,

Having regard to Regulation (EU) No 649/2012 of the European Parliament and of the Council of 4 July 2012 concerning the export and import of hazardous chemicalsf1, and in particular Article 22(1) thereof,

After consulting the Committee established by Article 133 of Regulation (EC) No 1907/2006 of the European Parliament and of the Council of 18 December 2006 concerning the Registration, Evaluation, Authorisation and Restriction of Chemicals (REACH), establishing a European Chemicals Agency, amending Directive 1999/45/EC and repealing Council Regulation (EEC) No 793/93 and Commission Regulation (EC) No 1488/94 as well as Council Directive 76/769/EEC and Commission Directives 91/155/EEC, 93/67/EEC, 93/105/EC and 2000/21/ECf2,

Whereas:

(1)

In order to ensure that information provided by the Member States is of a consistent standard, it is appropriate to create a common format to be used by the Member States in fulfilling their reporting obligations under Regulation (EU) No 649/2012.

(2)

It is appropriate to specify the exact reporting periods to ensure clarity and consistency as Regulation (EU) No 649/2012 requires Member States to forward the information concerning the operation of the procedures every three years,

HAS ADOPTED THIS DECISION:

Annotations to the whole text

Footnotes

f1

OJ L 201, 27.7.2012, p. 60.

f2

OJ L 396, 30.12.2006, p. 1.

Contents

  1. 1Article 1
  2. 2Article 2
  3. 3Article 3
  4. Signature
  5. Annex: QUESTIONNAIRE
  7. 1Division 1
  8. 2Division 2
  9. 3Division 3
  10. 4Division 4
  12. 5Division 5
  13. 6Division 6
  14. 7Division 7
  15. 8Division 8
  16. 9Division 9
  17. 10Division 10
  19. 11Division 11
  20. 12Division 12
  21. 13Division 13
  22. 14Division 14
  24. 15Division 15
  25. 16Division 16
  26. 17Division 17
  27. 18Division 18
  28. (Only relevant for Member States that processed export notifications in the reporting period.)
  29. 19Division 19
  30. 20Division 20
  31. 21Division 21
  32. Article 8(5) — export of a chemical relating to an emergency situation
  33. 22Division 22
  34. 23Division 23
  35. Article 8(7) — provision of available additional information concerning exported chemicals
  36. 24Division 24
  37. 25Division 25
  38. Article 8(8) — administrative fee for export notifications
  39. 26Division 26
  40. 27Division 27
  41. 28Division 28
  42. 29Division 29
  43. 30Division 30
  44. 31Division 31
  46. Exporters (Article 10)
  47. 32Division 32
  48. Importers (Article 10)
  49. 33Division 33
  50. 34Division 34
  51. Member State reporting to ECHA
  52. 35Division 35
  53. 36Division 36
  55. Communication of information and decisions to those concerned within the jurisdiction of your Member State (Article 14(3))
  56. 37Division 37
  57. Exporter compliance with decisions in each import response (Article 14(4))
  58. 38Division 38
  59. Provision of support to importing parties (Article 14(5))
  60. 39Division 39
  61. Substances that cannot be exported unless certain conditions are fulfilled (Article 14(6))
  62. 40Division 40
  63. 41Division 41
  64. 42Division 42
  65. 43Division 43
  66. 44Division 44
  67. DNAs decision that export may proceed 60 days after an explicit consent request was made (Article 14(7))
  68. 45Division 45
  69. 46Division 46
  70. Validity of explicit consent (Article 14(8))
  71. 47Division 47
  73. Import decisions made available to those concerned (Article 13(5))
  74. 48Division 48
  76. First transit movement information and time frame requirements (Article 16)
  77. 49Division 49
  78. 50Division 50
  80. 51Division 51
  81. 52Division 52
  82. 53Division 53
  83. 54Division 54
  84. 55Division 55
  86. Cooperation
  87. 56Division 56
  88. Capacity building
  89. 57Division 57
  91. General information
  92. 58Division 58
  93. 59Division 59
  94. 60Division 60
  95. 61Division 61
  96. Enforcement strategy
  97. 62Division 62
  98. 62(a)Division 62(a)
  99. 62(b)Division 62(b)
  100. Reporting on enforcement activities
  101. 63Division 63
  102. 64Division 64
  103. 65Division 65
  104. Power of enforcement authorities
  105. 66Division 66
  106. Details of infringements
  107. 67Division 67
  108. 68Division 68
  109. 69Division 69
  110. Penalties
  111. 70Division 70
  112. 71Division 71
  113. Collaboration
  114. 72Division 72
  115. 73Division 73
  116. 74Division 74
  117. 75Division 75
  118. 76Division 76
  119. Role of the Forum for Exchange of Information on Enforcement (‘the Forum’; see Article 18(2))
  120. 77Division 77
  121. 78Division 78
  123. DNAs and the ePIC system
  124. 79Division 79
  125. Exporters and the ePIC system
  126. 80Division 80
  127. Customs, other enforcement authorities and the ePIC system (optional)
  128. 81Division 81
  129. 82Division 82
  130. 83Division 83
  131. 84Division 84
  132. 85Division 85
  133. 86Division 86
  135. 87Division 87