juris

Pharmacy Act

consolidated text (as at 2004, amended since). juris shows the text as it was consolidated; it does not confirm that this is the law in force today.

Later amending instruments held: Business Facilitation (Miscellaneous Provisions) Act 2019 (Act No 14 of 2019), Covid-19 (Miscellaneous Provisions) Act 2020, Finance (Miscellaneous Provisions) Act 2020, Finance (Miscellaneous Provisions) Act 2021 (Act No 15 of 2021), Finance (Miscellaneous Provisions) Act 2022 (Act No 15 of 2022), Finance (Miscellaneous Provisions) Act 2023 (Act No 12 of 2023).

Ask juris about this law Official source

Sections

  1. 1 Short title
  2. 2 Interpretation
  3. PART II: BOARD AND COMMITTEES
  4. 3 Pharmacy Board
  5. 4 Functions of Board
  6. 5 Meetings of Board
  7. 6 Education Committee
  8. 6 Education Committee inserted by Act No 15 of 2021
  9. PART II: BOARD AND COMMITTEES
  10. 7 Trade and Therapeutics Committee
  11. 8 Poisons Committee
  12. 9 Planning Committee
  13. 10 Appointed members of committees
  14. PART III: REGISTRATION AND EXAMINATIONS
  15. 11 Registrar
  16. 12 Registration
  17. 13 Students
  18. 13 Pharmacy technician diploma inserted by Act No 15 of 2021
  19. PART III: REGISTRATION AND EXAMINATIONS
  20. 14 Admission to examinations
  21. 15 Pharmacist’s diploma
  22. 16 Examinations
  23. PART IV: PHARMACEUTICAL TRADE
  24. 17 Sale of pharmaceutical products
  25. 18 Operation of pharmacy
  26. 19 Death of pharmacist
  27. 20 Prescription Book
  28. 21 Prescriptions
  29. 22 Dispensing prescriptions
  30. 23 Wholesale pharmacy
  31. 24 Quality of pharmaceutical products
  32. 25 Import of drugs
  33. PART V: POISONS
  34. 26 Import of poisons
  35. 27 Sale of poisons
  36. 28 Exemption
  37. 29 Poisons Book
  38. PART VI: THERAPEUTIC SUBSTANCES
  39. 30 Import of therapeutic substances
  40. 31 Standards of therapeutic substances
  41. 32 Sale of therapeutic substances
  42. 33 Sale of antibiotics
  43. 34 Treatment
  44. PART VII: MANUFACTURE OF PHARMACEUTICAL PRODUCTS
  45. 35 Building of factory
  46. 36 Licence for manufacture
  47. 36B Sale of locally manufactured pharmaceutical inserted by Act No 1 of 2020
  48. 36C Registration of locally manufactured pharmaceutical inserted by Act No 1 of 2020
  49. PART VII: MANUFACTURE OF PHARMACEUTICAL PRODUCTS
  50. 37 Supervision of factory
  51. 38 Quality control
  52. 39 Storage, records and samples
  53. PART VIII: MISCELLANEOUS
  54. 40 Illegal arrangements
  55. 41 Advertising
  56. 42 Inspectors
  57. 43 Samples
  58. 44 Powers of Director-General
  59. 45 Offences
  60. 46 Application of Act
  61. 47 Regulations