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The Medicines for Human Use (Advanced Therapy Medicinal Products and Miscellaneous Amendments) Regulations 2010 (revoked)

S.I. 2010/1882 · Made 21 July 2010 · Extends to United Kingdom

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

Medicines

Made 21st July 2010

Laid before Parliament 26th July 2010

Coming into force 19th August 2010

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Annotations to the whole text

Textual amendments

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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  1. 1Citation, commencement and interpretation Repealed
  2. 2Disapplication of section 7 of the Medicines Act 1968 to exempt advanced therapy medicinal products Repealed
  3. 3Licence conditions for exempt advanced therapy medicinal products Repealed
  4. 4Traceability Repealed
  5. 5Traceability in the event of bankruptcy or liquidation of holder of manufacturer's licence for exempt ATMP Repealed
  6. 6Amendment of the Medicines (Standard Provisions for Licences and Certificates) Regulations 1971 Repealed
  7. 7Amendment of the Medicines (Applications for Manufacturer's and Wholesale Dealer's Licences) Regulations 1971 Repealed
  8. 8Amendment of the Medicines for Human Use (Marketing Authorisations Etc.) Regulations 1994 Repealed
  9. 9Amendment of the Medicines for Human Use (Clinical Trials) Regulations 2004 Repealed
  10. 10Amendment of the Medicines for Human Use (Manufacturing, Wholesale Dealing and Miscellaneous Amendments) Regulations 2005 Repealed
  11. Signature
  12. Schedule 1: Requirement that holders of manufacturer's licences comply with certain obligations in relation to the manufacture and assembly of exempt advanced therapy medicinal products Repealed
  13. Paragraph Repealed
  14. Schedule 2: Standard provisions for manufacturer's licences insofar as those licences relate to exempt advanced therapy medicinal products Repealed
  15. 1Paragraph 1 Repealed
  16. 2Paragraph 2 Repealed
  17. Schedule 3: Requirement that holders of wholesale dealer's licences comply with certain obligations in relation to exempt advanced therapy medicinal products Repealed
  18. Paragraph Repealed
  19. Schedule 4: Standard provisions for wholesale dealer's licences insofar as those licences relate to exempt advanced therapy medicinal products Repealed
  20. Paragraph Repealed
  21. Schedule 5: Amendments to the Medicines for Human Use (Marketing Authorisations Etc.) Regulations 1994 Repealed
  22. 1Amendment of regulation 1 Repealed
  23. 2Amendment of Schedule 1 Repealed
  24. 3Amendment of Schedule 3 Repealed
  25. 4Amendment of Schedule 6 Repealed
  26. Explanatory note

1Citation, commencement and interpretationF1

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2Disapplication of section 7 of the Medicines Act 1968 to exempt advanced therapy medicinal productsF1

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3Licence conditions for exempt advanced therapy medicinal productsF1

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4TraceabilityF1

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5Traceability in the event of bankruptcy or liquidation of holder of manufacturer's licence for exempt ATMPF1

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6Amendment of the Medicines (Standard Provisions for Licences and Certificates) Regulations 1971F1

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7Amendment of the Medicines (Applications for Manufacturer's and Wholesale Dealer's Licences) Regulations 1971F1

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8Amendment of the Medicines for Human Use (Marketing Authorisations Etc.) Regulations 1994F1

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9Amendment of the Medicines for Human Use (Clinical Trials) Regulations 2004F1

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10Amendment of the Medicines for Human Use (Manufacturing, Wholesale Dealing and Miscellaneous Amendments) Regulations 2005F1

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Signature

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1F1

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2F1

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1Amendment of regulation 1F1

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2Amendment of Schedule 1F1

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3Amendment of Schedule 3F1

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4Amendment of Schedule 6F1

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Explanatory note

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