Commonwealth Numbered Acts
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THERAPEUTIC GOODS ACT 1989
TABLE OF PROVISIONS
Long Title
1. Short title
2. Commencement
3. Interpretation
4. Object of Act
5. Act to bind Crown
6. Operation of Act
7. Goods may be declared to be or not to be therapeutic goods
8. Power to obtain information with respect to therapeutic goods
9. Arrangements with States etc.
10. Determination of standards
11. Date of effect of standards
12. Standards to be disallowable
13. Special provisions relating to standards
14. Compliance with standards
15. Consent may be subject to conditions etc.
16. Forms etc. of therapeutic goods
17. Australian Register of Therapeutic Goods
18. Exempt goods
19. Exemptions for special and experimental uses
20. Offences by sponsors
21. Offence relating to wholesale supply
22. General offences relating to this Part
23. Applications generally
24. Applications for registration
25. Evaluation of therapeutic goods
26. Listing of therapeutic goods
27. Registration or listing number
28. Conditions on registration or listing
29. Duration of registration or listing
30. Cancellation of registration or listing
31. Secretary may require information
32. Inspection and variation of entries in Register
33. Publication of list of goods on Register
34. Exempt goods and exempt persons
35. Offences relating to manufacturing and licences
36. Manufacturing principles
37. Application for licence
38. Grant of licence
39. Term of licence
40. Conditions of licences
41. Revocation and suspension of licences
42. Publication of list of manufacturers etc.
43. By whom charges payable
44. Time for payment of charges
45. Money to be paid into trust account
46. Monitoring compliance with Act
47. Entry and search of premises - evidence of offences
48. General powers of authorised persons in relation to premises
49. Monitoring warrants
50. Offence related warrants
51. Offence related warrants by telephone
52. Identity cards
53. Retention of material on withdrawal of applications
54. Offences
55. Conduct by directors, servants and agents
56. Judicial notice
57. Delegation
58. Export certifications
59. Fees
60. Review of decisions
61. Release of information
62. Consequential amendments
63. Regulations
64. Interpretation
65. Repeal
66. Transitional arrangements for goods required to be registered or listed
67. Transitional provision for therapeutic goods for export only
68. Transitional arrangements for Part 4
69. Continuation of standards and requirements
SCHEDULE
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