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Regulation (EC) No 726/2004 of the European Parliament and of the Council of 31 March 2004 laying down Union procedures for the authorisation and supervision of medicinal products for human and veterinary use and establishing a European Medicines Agency (Text with EEA relevance) (revoked)

EU Regulation No 726/2004 · Adopted 31 March 2004 · 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.

Regulation (EC) No 726/2004 of the European Parliament and of the Council

of 31 March 2004

laying down Union procedures for the authorisation and supervision of medicinal products for human and veterinary use and establishing a European Medicines Agency

(Text with EEA relevance) (revoked)

F1. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

Annotations to the whole text

Textual amendments

F1

Regulation revoked insofar as it applies to medicinal products for veterinary use (31.12.2020) by The Veterinary Medicines and Animals and Animal Products (Examination of Residues and Maximum Residue Limits) (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/676), regs. 1(2)(b), 5; 2020 c. 1, Sch. 5 para. 1(1)

Regulation revoked insofar as it applies to medicinal products for human use (31.12.2020) by The Human Medicines (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/775), Sch. 9 para. 1(h) (subject to transitional provisions in S.I. 2012/1916, Sch. 33A); 2020 c. 1, Sch. 5 para. 1(1)

Contents

  1. Title I: DEFINITIONS AND SCOPE Repealed
  2. 1Article 1 Repealed
  3. 2Article 2 Repealed
  4. 3Article 3 Repealed
  5. 4Article 4 Repealed
  6. Title II: AUTHORISATION AND SUPERVISION OF MEDICINAL PRODUCTS FOR HUMAN USE Repealed
  7. Chapter 1: Submission and examination of applications — Authorisations Repealed
  8. 5Article 5 Repealed
  9. 6Article 6 Repealed
  10. 7Article 7 Repealed
  11. 8Article 8 Repealed
  12. 9Article 9 Repealed
  13. 10Article 10 Repealed
  14. 10aArticle 10a Repealed
  15. 10bArticle 10b Repealed
  16. 11Article 11 Repealed
  17. 12Article 12 Repealed
  18. 13Article 13 Repealed
  19. 14Article 14 Repealed
  20. 14-aArticle 14-a Repealed
  21. 14aArticle 14a Repealed
  22. 14bArticle 14b Repealed
  23. 15Article 15 Repealed
  24. Chapter 2: Supervision and penalties Repealed
  25. 16Article 16 Repealed
  26. 16aArticle 16a Repealed
  27. 16bArticle 16b Repealed
  28. 17Article 17 Repealed
  29. 18Article 18 Repealed
  30. 19Article 19 Repealed
  31. 20Article 20 Repealed
  32. 20aArticle 20a Repealed
  33. Chapter 3: Pharmacovigilance Repealed
  34. 21Article 21 Repealed
  35. 22Article 22 Repealed
  36. 23Article 23 Repealed
  37. 24Article 24 Repealed
  38. 25Article 25 Repealed
  39. 25aArticle 25a Repealed
  40. 26Article 26 Repealed
  41. 27Article 27 Repealed
  42. 28Article 28 Repealed
  43. 28aArticle 28a Repealed
  44. 28bArticle 28b Repealed
  45. 28cArticle 28c Repealed
  46. 28dArticle 28d Repealed
  47. 28eArticle 28e Repealed
  48. 28fArticle 28f Repealed
  49. 29Article 29 Repealed
  50. Title III: AUTHORISATION AND SUPERVISION OF VETERINARY MEDICINAL PRODUCTS Repealed
  51. Chapter 1: Submission and examination of applications — Authorisations Repealed
  52. 30Article 30 Repealed
  53. 31Article 31 Repealed
  54. 32Article 32 Repealed
  55. 33Article 33 Repealed
  56. 34Article 34 Repealed
  57. 35Article 35 Repealed
  58. 36Article 36 Repealed
  59. 37Article 37 Repealed
  60. 38Article 38 Repealed
  61. 39Article 39 Repealed
  62. 40Article 40 Repealed
  63. Chapter 2: Supervision and sanctions Repealed
  64. 41Article 41 Repealed
  65. 42Article 42 Repealed
  66. 43Article 43 Repealed
  67. 44Article 44 Repealed
  68. 45Article 45 Repealed
  69. Chapter 3: Pharmacovigilance Repealed
  70. 46Article 46 Repealed
  71. 47Article 47 Repealed
  72. 48Article 48 Repealed
  73. 49Article 49 Repealed
  74. 50Article 50 Repealed
  75. 51Article 51 Repealed
  76. 52Article 52 Repealed
  77. 53Article 53 Repealed
  78. 54Article 54 Repealed
  79. Title IV: THE EUROPEAN MEDICINES AGENCY — RESPONSIBILITIES AND ADMINISTRATIVE STRUCTURE Repealed
  80. Chapter 1: Tasks of the Agency Repealed
  81. 55Article 55 Repealed
  82. 56Article 56 Repealed
  83. 57Article 57 Repealed
  84. 58Article 58 Repealed
  85. 59Article 59 Repealed
  86. 60Article 60 Repealed
  87. 61Article 61 Repealed
  88. 61aArticle 61a Repealed
  89. 62Article 62 Repealed
  90. 63Article 63 Repealed
  91. 64Article 64 Repealed
  92. 65Article 65 Repealed
  93. 66Article 66 Repealed
  94. Chapter 2: Financial Provisions Repealed
  95. 67Article 67 Repealed
  96. 68Article 68 Repealed
  97. 69Article 69 Repealed
  98. 70Article 70 Repealed
  99. Chapter 3: General Provisions governing the Agency Repealed
  100. 71Article 71 Repealed
  101. 71aThe Agency shall have its seat in Amsterdam, the Netherlands. Repealed
  102. 72Article 72 Repealed
  103. 73Article 73 Repealed
  104. 73aArticle 73a Repealed
  105. 74Article 74 Repealed
  106. 75Article 75 Repealed
  107. 76Article 76 Repealed
  108. 77Article 77 Repealed
  109. 78Article 78 Repealed
  110. 79Article 79 Repealed
  111. 80Article 80 Repealed
  112. Title V: GENERAL AND FINAL PROVISIONS Repealed
  113. 81Article 81 Repealed
  114. 82Article 82 Repealed
  115. 83Article 83 Repealed
  116. 84Article 84 Repealed
  117. 84aArticle 84a Repealed
  118. 85Article 85 Repealed
  119. 86Article 86 Repealed
  120. 86aArticle 86a Repealed
  121. 87Article 87 Repealed
  122. 87aArticle 87a Repealed
  123. 87bArticle 87b Repealed
  124. 87cArticle 87c Repealed
  125. 87dArticle 87d Repealed
  126. 88Article 88 Repealed
  127. 89Article 89 Repealed
  128. 90Article 90 Repealed
  129. Signature
  130. Annex I: MEDICINAL PRODUCTS TO BE AUTHORISED BY THE UNION Repealed
  131. 1Division 1 Repealed
  132. 1aDivision 1a Repealed
  133. 2Division 2 Repealed
  134. 3Division 3 Repealed
  135. 4Division 4 Repealed
  136. Annex IILIST OF THE OBLIGATIONS REFERRED TO IN ARTICLE 84A Repealed