OpenLegislation

Grant etc of licences Grant etc of licences

  1. 17Manufacturing of medicinal products
  2. 17AManufacturing of MM medicinal products
  3. 17BManufacturing of POC medicinal products
  4. 18Wholesale dealing in medicinal products
  5. 18AApproved country for import
  6. 19Exemptions from requirement for wholesale dealer's licence
  7. 20Mixing of medicines
  8. 21Application for manufacturer's or wholesale dealer's licence
  9. 22Factors relevant to determination of application for manufacturer's or wholesale dealer's licence
  10. 23Grant or refusal of licence
  11. 24Standard provisions of licences
  12. 25Duration of licence
  13. 26General power to suspend, revoke or vary licences
  14. 27Procedure where licensing authority proposes to suspend, revoke or vary licence
  15. 27AEffect of suspension or variation relating to modular unit or POC site
  16. 28Suspension of licence in cases of urgency
  17. 29Variation of licence on the application of the holder
  18. 29AVariation of MM master file
  19. 29BVariation of POC master file
  20. 30Provision of information

Notes on Part 3

Textual amendments

F1

Pt. 3 heading and Pt. 3 Ch. 1 inserted (20.8.2013) by The Human Medicines (Amendment) Regulations 2013 (S.I. 2013/1855), regs. 1(1), 4

Notes on Chapter 2

Textual amendments

F1

Pt. 3 Ch. 2 heading inserted (20.8.2013) by The Human Medicines (Amendment) Regulations 2013 (S.I. 2013/1855), regs. 1(1), 4