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The Medicines for Human Use (Manufacturing, Wholesale Dealing and Miscellaneous Amendments) Regulations 2005 (revoked)

S.I. 2005/2789 · Made 10 October 2005 · Extends to United Kingdom

Up to date with all changes known to legislation.gov.uk, revised to 14 August 2012.

MEDICINES

Made 10th October 2005

Laid before Parliament 10th October 2005

Coming into force 30th October 2005

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Annotations to the whole text

Textual amendments

F1

Regulations revoked (14.8.2012) by The Human Medicines Regulations 2012 (S.I. 2012/1916), reg. 1(2), Sch. 35 (with Sch. 32)

Contents

  1. 1Citation, commencement and interpretation Repealed
  2. 2Requirement that manufacturer's licence holders comply with certain obligations in relation to the manufacture and assembly of relevant medicinal products Repealed
  3. 3Requirement that manufacturer's licence holders comply with certain obligations in relation to the import from a third country of relevant medicinal products Repealed
  4. 4Requirements as to qualified persons Repealed
  5. 5Offence relating to the sale and supply of starting materials for use in the manufacture of relevant medicinal products Repealed
  6. 6Standard provisions for manufacturer's licences Repealed
  7. 7Additional standard provisions for manufacturers licences which relate to vaccines, toxins and sera Repealed
  8. 8Requirement that holders of wholesale dealer's licences comply with certain obligations Repealed
  9. 9Requirement that wholesale dealers deal only with specified persons Repealed
  10. 10Requirement as to responsible persons Repealed
  11. 11Standard provisions for wholesale dealer's licences Repealed
  12. 12Application of these Regulations to manufacturer's and wholesale dealer's licences Repealed
  13. 13Consequential and other amendments to enactments Repealed
  14. 14Revocations Repealed
  15. 15Transitional provisions Repealed
  16. Signature
  17. Schedule 1: STANDARD PROVISIONS WHICH MAY BE INCORPORATED IN A MANUFACTURER'S LICENCE RELATING TO THE MANUFACTURE AND ASSEMBLY OF RELEVANT MEDICINAL PRODUCTS Repealed
  18. 1Paragraph 1 Repealed
  19. 2Paragraph 2 Repealed
  20. 3Paragraph 3 Repealed
  21. 4Paragraph 4 Repealed
  22. 5Paragraph 5 Repealed
  23. 6Paragraph 6 Repealed
  24. 7Paragraph 7 Repealed
  25. 8Paragraph 8 Repealed
  26. 9Paragraph 9 Repealed
  27. 10Paragraph 10 Repealed
  28. 11Paragraph 11 Repealed
  29. 12Paragraph 12 Repealed
  30. 13Paragraph 13 Repealed
  31. Schedule 2: STANDARD PROVISIONS WHICH MAY BE INCORPORATED IN A MANUFACTURER'S LICENCE RELATING TO THE IMPORT OF RELEVANT MEDICINAL PRODUCTS FROM A THIRD COUNTRY Repealed
  32. 1Paragraph 1 Repealed
  33. 2Paragraph 2 Repealed
  34. 3Paragraph 3 Repealed
  35. 4Paragraph 4 Repealed
  36. 5Paragraph 5 Repealed
  37. 6Paragraph 6 Repealed
  38. 7Paragraph 7 Repealed
  39. 8Paragraph 8 Repealed
  40. Schedule 3: STANDARD PROVISIONS WHICH MAY BE INCORPORATED IN A MANUFACTURER'S LICENCE WHICH RELATES TO VACCINES, TOXINS OR SERA Repealed
  41. Part 1: STANDARD PROVISIONS WHICH MAY BE INCORPORATED IN A MANUFACTURER'S LICENCE WHICH RELATES TO VACCINES Repealed
  42. 1Paragraph 1 Repealed
  43. 2Paragraph 2 Repealed
  44. 3Paragraph 3 Repealed
  45. 4Paragraph 4 Repealed
  46. 5Paragraph 5 Repealed
  47. 6Paragraph 6 Repealed
  48. 7Paragraph 7 Repealed
  49. 8Paragraph 8 Repealed
  50. Part 2: STANDARD PROVISIONS WHICH MAY BE INCORPORATED IN A MANUFACTURER'S LICENCE WHICH RELATES TO SMALLPOX VACCINES Repealed
  51. 1Paragraph 1 Repealed
  52. 2Paragraph 2 Repealed
  53. 3Paragraph 3 Repealed
  54. Part 3: STANDARD PROVISIONS WHICH MAY BE INCORPORATED IN A MANUFACTURER'S LICENCE WHICH RELATES TO BCG VACCINES Repealed
  55. 1Paragraph 1 Repealed
  56. 2Paragraph 2 Repealed
  57. 3Paragraph 3 Repealed
  58. 4Paragraph 4 Repealed
  59. 5Paragraph 5 Repealed
  60. 6Paragraph 6 Repealed
  61. Part 4: STANDARD PROVISIONS WHICH MAY BE INCORPORATED IN A MANUFACTURER'S LICENCE WHICH RELATES TO TOXINS Repealed
  62. 1Paragraph 1 Repealed
  63. 2Paragraph 2 Repealed
  64. 3Paragraph 3 Repealed
  65. Part 5: STANDARD PROVISIONS WHICH MAY BE INCORPORATED IN A MANUFACTURER'S LICENCE WHICH RELATES TO SERA Repealed
  66. 1Paragraph 1 Repealed
  67. 2Paragraph 2 Repealed
  68. 3Paragraph 3 Repealed
  69. 4Paragraph 4 Repealed
  70. 5Paragraph 5 Repealed
  71. 6Paragraph 6 Repealed
  72. 7Paragraph 7 Repealed
  73. 8Paragraph 8 Repealed
  74. 9Paragraph 9 Repealed
  75. Schedule 4: STANDARD PROVISIONS WHICH MAY BE INCORPORATED IN A WHOLESALE DEALER'S LICENCE Repealed
  76. 1Paragraph 1 Repealed
  77. 2Paragraph 2 Repealed
  78. 3Paragraph 3 Repealed
  79. 4Paragraph 4 Repealed
  80. Schedule 5: CONSEQUENTIAL AND OTHER AMENDMENTS OF ENACTMENTS Repealed
  81. Part 1: AMENDMENTS TO THE ACT Repealed
  82. 1Paragraph 1 Repealed
  83. 2Paragraph 2 Repealed
  84. 3Paragraph 3 Repealed
  85. 4Paragraph 4 Repealed
  86. 5Paragraph 5 Repealed
  87. 6Paragraph 6 Repealed
  88. 7Paragraph 7 Repealed
  89. 8Paragraph 8 Repealed
  90. 9Paragraph 9 Repealed
  91. 10Paragraph 10 Repealed
  92. Part 2: AMENDMENTS TO ORDERS AND REGULATIONS Repealed
  93. 1Amendments to the Standard Provisions Regulations Repealed
  94. 2Amendments to the Applications Regulations Repealed
  95. 3Amendments to the Medicines (Renewal Applications for Licences and Certificates) Regulations 1974 Repealed
  96. 4Amendments to the Medicines (Retail Sale or Supply of Herbal Remedies) Order 1977 Repealed
  97. Schedule 6: TRANSITIONAL PROVISIONS Repealed
  98. 1Wholesale dealer's licences granted before 30th October 2005 relating to the import of medicinal products from third countries Repealed
  99. 2Applications for wholesale dealer's licences made before 30th October 2005 Repealed
  100. 3Manufacturer's and wholesale dealer's licences granted before 30th October 2005 Repealed
  101. Explanatory note