Legislation, Legislation In force, Western Australian Legislation
Gene Technology Act 2006 (WA)
An Act to regulate activities involving gene technology and for other purposes.
Western Australia
Gene Technology Act 2006
Western Australia
Gene Technology Act 2006
Contents
Part 1 — Preliminary
1. Purpose and short title 2
2. Commencement 2
3. Object of Act 2
4. Regulatory framework to achieve object 2
5. Nationally consistent scheme 3
6. Act to bind the Crown 3
7. External Territories 3
8. Offences 3
8A. Numbering 4
8B. Notes 4
8C. Outlines 4
Part 2 — Interpretation and operation of Act
Division 1 — Simplified outline
9. Simplified outline 5
Division 2 — Definitions
10. Definitions 5
11. Meaning of intentional release of a GMO into the environment 11
12. Meaning of corresponding State law 11
12A. Meaning of reckless 11
Division 3 — Operation of Act
13. Operation of Act 12
14. Wind‑back of reach of Act 12
15. Relationship to other State laws 12
Division 4 — Provisions to facilitate a nationally consistent scheme
Subdivision A — General provisions
16. State laws may operate concurrently 13
17. Conferral of functions on Commonwealth officers and bodies 13
18. No doubling‑up of liabilities 13
19. Review of certain decisions 13
20. Things done for multiple purposes 14
Subdivision B — Policy principles, policy guidelines and codes of practice
21. Ministerial Council may issue policy principles 14
22. Consultation on policy principles 15
23. Ministerial Council may issue policy guidelines 15
24. Ministerial Council may issue codes of practice 16
Part 3 — The Gene Technology Regulator
25. Simplified outline 17
26. The Gene Technology Regulator 17
27. Functions of the Regulator 17
28. Powers of the Regulator 18
29. Delegation 18
30. Independence of the Regulator 19
Part 4 — Regulation of dealings with GMOs
Division 1 — Simplified outline
31. Simplified outline 20
Division 2 — Dealings with GMOs must be licensed
32. Person not to deal with a GMO without a licence 20
33. Person not to deal with a GMO without a licence — strict liability offence 22
34. Person must not breach conditions of a GMO licence 22
35. Person must not breach conditions of a GMO licence — strict liability offence 24
36. Person must not breach conditions on GMO Register 24
37. Offence relating to notifiable low risk dealings 25
38. Aggravated offences — significant damage to health or safety of people or to the environment 25
Part 5 — Licensing system
Division 1 — Simplified outline
39. Simplified outline 26
Division 2 — Licence applications
40. Person may apply for a licence 26
41. Application may be withdrawn 27
42. Regulator may require applicant to give further information 27
43. Regulator must consider applications except in certain circumstances 28
44. Regulator may consult with applicant 28
45. Regulator must not use certain information in considering licence application 28
Division 3 — Initial consideration of licences for dealings not involving intentional release of a GMO into the environment
46. Applications to which this Division applies 29
47. What the Regulator must do in relation to application 29
Division 4 — Initial consideration of licences for dealings involving intentional release of a GMO into the environment
48. Applications to which this Division applies 30
49. Dealings that may pose significant risks to the health and safety of people or the environment 30
50. Regulator must prepare risk assessment and risk management plan 32
51. Matters Regulator must take into account in preparing risk assessment and risk management plan 32
52. Public notification of risk assessment and risk management plan 34
53. Regulator may take other actions 35
54. Person may request copies of certain documents 36
Division 5 — Decision on licence etc.
55. Regulator must make a decision on licence and licence conditions 36
56. Regulator must not issue the licence unless satisfied as to risk management 36
57. Other circumstances in which Regulator must not issue the licence 37
58. Matters to be taken into account in deciding whether a person is suitable to hold a licence 38
59. Notification of licence decision 39
60. Period of licence 39
Division 6 — Conditions of licence
61. Licence is subject to conditions 40
62. Conditions that may be prescribed or imposed 40
63. Condition about informing people of obligations 41
64. Condition about monitoring and audits 42
65. Condition about additional information to be given to the Regulator 42
66. Person may give information to Regulator 43
67. Protection of persons who give information 43
Division 7 — Suspension, cancellation and variation of licences
68. Suspension and cancellation of licence 43
69. Surrender of licence 44
70. Transfer of licence 44
71. Variation of licence 45
72. Regulator to notify of proposed suspension, cancellation or variation 46
Division 8 — Annual charge
72A. GMO licence — annual charge 47
Part 6 — Regulation of notifiable low risk dealings and dealings on the GMO Register
Division 1 — Simplified outline
73. Simplified outline 48
Division 2 — Notifiable low risk dealings
74. Notifiable low risk dealings 48
75. Regulation of notifiable low risk dealings 49
Division 3 — The GMO Register
76. The GMO Register 50
77. Contents of Register 50
78. Regulator may include dealings with GMOs on GMO Register 50
79. Regulator not to make determination unless risks can be managed 51
80. Variation of GMO Register 52
81. Inspection of Register 52
Part 7 — Certification and accreditation
Division 1 — Simplified outline
82. Simplified outline 53
Division 2 — Certification
83. Application for certification 53
84. When the Regulator may certify the facility 53
85. Regulator may require applicant to give further information 54
86. Conditions of certification 54
87. Variation of certification 54
88. Suspension or cancellation of certification 54
89. Regulator to notify of proposed suspension, cancellation or variation 55
90. Guidelines 56
Division 3 — Accredited organisations
91. Application for accreditation 56
92. Regulator may accredit organisations 56
93. Regulator may require applicant to give further information 57
94. Conditions of accreditation 57
95. Variation of accreditation 57
96. Suspension or cancellation of accreditation 58
97. Regulator to notify of proposed suspension, cancellation or variation 58
98. Guidelines 59
Part 8 — The Gene Technology Technical Advisory Committee, the Gene Technology Community Consultative Group and the Gene Technology Ethics Committee
Division 1 — Simplified outline
99. Simplified outline 60
Division 2 — The Gene Technology Technical Advisory Committee
100. The Gene Technology Technical Advisory Committee 60
101. Function of the Gene Technology Technical Advisory Committee 60
102. Expert advisers 61
103. Remuneration 61
104. Members and procedures 61
105. Subcommittees 61
Division 3 — The Gene Technology Community Consultative Committee
106. The Gene Technology Community Consultative Committee 61
107. Function of Consultative Committee 62
108. Membership 62
109. Remuneration 62
110. Regulations 62
110A. Subcommittees 62
Division 4 — The Gene Technology Ethics Committee
111. The Gene Technology Ethics Committee 63
112. Function of the Gene Technology Ethics Committee 63
113. Expert advisers 63
114. Remuneration 63
115. Members and procedures 63
116. Subcommittees 64
Part 9 — Administration
Division 1 — Simplified outline
117. Simplified outline 65
Division 2 — Appointment and conditions of Regulator
118. Appointment of the Regulator 65
119. Termination of appointment 65
120. Disclosure of interests 65
121. Acting appointment 66
122. Terms and conditions 66
123. Outside employment 66
124. Remuneration 66
125. Leave of absence 66
126. Resignation 66
Division 3 — Money
127. Regulator may charge for services 66
128. Notional payments by the State 67
129. Gene Technology Account 67
130. Credits to Gene Technology Account 67
131. Recovery of amounts 68
132. Purposes of Account 68
Division 4 — Staffing
133. Staff assisting the Regulator 68
134. Consultants 68
135. Seconded officers 69
Division 5 — Reporting requirements
136. Annual report 69
136A. Quarterly reports 69
137. Reports to Parliament 70
Division 6 — Record of GMO and GM product dealings
138. Record of GMO and GM product dealings 70
139. Inspection of Record 71
Division 7 — Reviews of notifiable low risk dealings and exemptions
140. Regulator may review notifiable low risk dealings 71
141. Regulator may review exemptions 72
142. Regulator may give notice of consideration 72
143. What Regulator may do after consideration 73
144. Regulator not required to review matters 73
Part 10 — Enforcement
145. Simplified outline 74
146. Regulator may give directions 74
147. Injunctions 76
148. Forfeiture 77
Part 11 — Powers of inspection
Division 1 — Simplified outline
149. Simplified outline 78
Division 2 — Appointment of inspectors and identity cards
150. Appointment of inspectors 78
151. Identity card 79
Division 3 — Monitoring powers
152. Powers available to inspectors for monitoring compliance 79
153. Monitoring powers 80
Division 4 — Offence‑related powers
154. Searches and seizures related to offences 81
155. Offence‑related powers of inspectors in relation to premises 82
156. Use of equipment at premises 83
Division 5 — Expert assistance
157. Expert assistance to operate a thing 84
Division 6 — Emergency powers
158. Powers available to inspectors for dealing with dangerous situations 85
Division 7 — Obligations and incidental powers of inspectors
159. Inspector must produce identity card on request 86
160. Consent 86
161. Details of warrant to be given to occupier etc. 86
162. Announcement before entry 87
163. Compensation for damage 87
Division 8 — Power to search goods, baggage etc.
164. Power to search goods, baggage etc. 88
165. Seizure of goods 88
Division 9 — General provisions relating to search and seizure
166. Copies of seized things to be provided 89
167. Occupier entitled to be present during search 89
168. Receipts for things seized 90
169. Retention of seized things 90
170. Magistrate may permit a thing to be retained 91
171. Disposal of goods if there is no owner or owner cannot be located 92
Division 10 — Warrants
172. Monitoring warrants 92
173. Offence‑related warrants 93
174. Offence‑related warrants by telephone, telex, fax etc. 94
175. Offences relating to warrants 96
Division 11 — Other matters
176. Part not to abrogate privilege against self‑incrimination 97
177. Part does not limit power to impose licence conditions 97
Part 12 — Miscellaneous
Division 1 — Simplified outline
178. Simplified outline 98
Division 2 — Review of decisions
179. Meaning of terms 98
180. Notification of decisions and review rights 99
181. Internal review 100
182. Deadlines for making reviewable decisions 100
183. Review of decisions by Administrative Appeals Tribunal 101
183A. Extended standing for judicial review 101
Division 3 — Confidential commercial information
184. Application for protection of confidential commercial information 101
185. Regulator may declare that information is confidential commercial information 101
186. Revocation of declaration 103
187. Confidential commercial information must not be disclosed 104
Division 4 — Conduct by directors, employees and agents
188. Conduct by directors, employees and agents 106
189. Meaning of terms 107
Division 5 — Transitional provisions
190. Transitional provision — dealings covered by Genetic Manipulation Advisory Committee advice to proceed 108
191. Regulations may relate to transitional matters 109
Division 6 — Other
192. False or misleading information or document 109
192A. Interference with dealings with GMOs 110
192B. Ancillary offences (parties to offences, attempts, incitement or conspiracy) 111
193. Regulations: general 111
194. Review of operation of Act 112
Part 13 — Consequential amendments
195. Agricultural and Veterinary Chemicals (Western Australia) Act 1995 amended 113
23A. Consultation with Gene Technology Regulator 113
Notes
Compilation table 115
Defined terms
Western Australia
Gene Technology Act 2006
An Act to regulate activities involving gene technology and for other purposes.
The Parliament of Western Australia enacts as follows:
Part 1 — Preliminary
1. Purpose and short title
(1) This is the Gene Technology Act 2006.
(2) The purpose of this Act is to regulate activities involving gene technology.
(3) Without limiting subsection (1) and section 26(1) of the Interpretation Act 1984, this Act may be referred to as the Gene Technology Law of Western Australia or simply as the Gene Technology Law.
Note for this section:
This section differs from section 1 of the Commonwealth Act.
2. Commencement
(1) This Act comes into operation on a day fixed by proclamation.
(2) Different days may be fixed under subsection (1) for different provisions.
Note for this section:
This section differs from section 2 of the Commonwealth Act.
3. Object of Act
The object of this Act is to protect the health and safety of people, and to protect the environment, by identifying risks posed by or as a result of gene technology, and by managing those risks through regulating certain dealings with genetically modified organisms.
4. Regulatory framework to achieve object
The object of this Act is to be achieved through a regulatory framework which —
(aa) provides that where there are threats of serious or irreversible environmental damage, a lack of full scientific certainty should not be used as a reason for postponing cost‑effective measures to prevent environmental degradation;
(a) provides an efficient and effective system for the application of gene technologies; and
(b) operates in conjunction with other Commonwealth and State regulatory schemes relevant to GMOs and GMO products.
Note for this section:
Examples of the schemes mentioned in paragraph (b) are those that regulate food, agricultural and veterinary chemicals, industrial chemicals and therapeutic goods.
5. Nationally consistent scheme
It is the intention of the Parliament that this Act form a component of a nationally consistent scheme for the regulation of certain dealings with genetically modified organisms by the Commonwealth and the States.
6. Act to bind the Crown
(1) This Act binds the Crown in right of Western Australia and, so far as the legislative power of the Parliament permits, the Crown in all its other capacities.
(2) Nothing in this Act renders the Crown liable to be prosecuted for an offence.
7. External Territories
Note for this section:
The Commonwealth Act includes a provision extending that Act to every external Territory other than Norfolk Island.
8. Offences
Note for this section:
The Commonwealth Act includes a provision applying Chapter 2 of The Criminal Code to offences against that Act and construing penalty provisions in that Act.
8A. Numbering
(1) In order to maintain consistent numbering between this Act and the Gene Technology Act 2000 of the Commonwealth —
(a) if the Commonwealth Act contains a section that is not required in this Act, the provision number and heading to the section appearing in the Commonwealth Act are included in this Act despite the omission of the body of the section; and
(b) if this Act contains a section that is not included in the Commonwealth Act, the section is numbered so as to maintain consistency in numbering between sections common to both Acts.
(2) A provision number and heading referred to in subsection (1)(a) form part of this Act.
Notes for this section:
1. A note appears under each heading of a kind referred to in subsection (1)(a) describing the omitted section of the Commonwealth Act.
2. A note appears under each section of a kind referred to in subsection (1)(b) highlighting the non‑appearance of an equivalent section in the Commonwealth Act.
3. This section does not appear in the Commonwealth Act.
8B. Notes
Notes do not form part of this Act.
Note for this section:
This section does not appear in the Commonwealth Act.
8C. Outlines
The provisions appearing at the beginning of Parts 2 to 12 outlining that Part (simplified outlines) are intended only as a guide to readers as to the general scheme and effect of that Part.
Note for this section:
This section does not appear in the Commonwealth Act.
Part 2 — Interpretation and operation of Act
Division 1 — Simplified outline
9. Simplified outline
In outline this Part —
* contains the definitions used in this Act;
* contains provisions to facilitate a nationally consistent regulatory scheme;
* enables the Ministerial Council to issue policy principles, policy guidelines and codes of practice.
Note for this section:
This section differs from section 9 of the Commonwealth Act.
Division 2 — Definitions
10. Definitions
(1) In this Act —
accredited organisation means an organisation accredited under Part 7 Division 3;
Administrative Appeals Tribunal means the Administrative Appeals Tribunal established by the Administrative Appeals Tribunal Act 1975 of the Commonwealth;
aggravated offence has the meaning given by section 38;
Commonwealth Act means the Gene Technology Act 2000 of the Commonwealth;
Commonwealth authority means the following —
(a) a body corporate established for a public purpose by or under a Commonwealth Act; or
(b) a company in which a controlling interest is held by any one of the following persons, or by 2 or more of the following persons together —
(i) the Commonwealth;
(ii) a body covered by paragraph (a);
(iii) a body covered by either of the above subparagraphs;
Commonwealth Environment Minister means the Minister of State for the Commonwealth responsible for environment and conservation;
confidential commercial information means information declared by the Regulator to be confidential commercial information under section 185;
Consultative Committee means the Gene Technology Community Consultative Committee established by section 106 of the Commonwealth Act;
containment level, in relation to a facility, means the degree of physical confinement of GMOs provided by the facility, having regard to the design of the facility, the equipment located or installed in the facility and the procedures generally used within the facility;
deal with, in relation to a GMO, means the following —
(a) conduct experiments with the GMO;
(b) make, develop, produce or manufacture the GMO;
(c) breed the GMO;
(d) propagate the GMO;
(e) use the GMO in the course of manufacture of a thing that is not the GMO;
(f) grow, raise or culture the GMO; or
(g) import the GMO,
and includes the possession, supply, use, transport or disposal of the GMO for the purposes of, or in the course of, a dealing mentioned in any of paragraphs (a) to (g);
eligible person, in relation to a reviewable decision, has the meaning given by section 179;
environment includes —
(a) ecosystems and their constituent parts;
(b) natural and physical resources; and
(c) the qualities and characteristics of locations, places and areas;
Ethics Committee means the Gene Technology Ethics Committee established by section 111 of the Commonwealth Act;
evidential material means any of the following —
(a) a thing with respect to which an offence against this Act or the regulations has been committed or is suspected, on reasonable grounds, to have been committed;
(b) a thing that there are reasonable grounds for suspecting will afford evidence as to the commission of any such offence;
(c) a thing that there are reasonable grounds for suspecting is intended to be used for the purpose of committing any such offence;
facility includes, but is not limited to, the following —
(a) a building or part of a building;
(b) a laboratory;
(c) an aviary;
(d) a glasshouse;
(e) an insectary;
(f) an animal house;
(g) an aquarium or tank;
gene technology means any technique for the modification of genes or other genetic material, but does not include —
(a) sexual reproduction;
(b) homologous recombination; or
(c) any other technique specified in the regulations for the purposes of this paragraph;
Gene Technology Account means the Gene Technology Account established by section 129 of the Commonwealth Act;
Gene Technology Agreement means the Gene Technology Intergovernmental Agreement made for the purposes of this Act between the Commonwealth and at least 4 States, as in force from time to time;
Gene Technology Technical Advisory Committee means the Gene Technology Technical Advisory Committee established by section 100 of the Commonwealth Act;
genetically modified organism means —
(a) an organism that has been modified by gene technology;
(b) an organism that has inherited particular traits from an organism (the initial organism), being traits that occurred in the initial organism because of gene technology; or
(c) anything declared by the regulations to be a genetically modified organism, or that belongs to a class of things declared by the regulations to be genetically modified organisms,
but does not include —
(d) a human being, if the human being is covered by paragraph (a) only because the human being has undergone somatic cell gene therapy; or
(e) an organism declared by the regulations not to be a genetically modified organism, or that belongs to a class of organisms declared by the regulations not to be genetically modified organisms;
GMO means a genetically modified organism;
GMO licence means a licence issued under section 55;
GMO Register means the GMO Register established by section 76 of the Commonwealth Act;
GM product means a thing (other than a GMO) derived or produced from a GMO;
Institutional Biosafety Committee means a committee established by an accredited organisation as an Institutional Biosafety Committee;
jurisdiction means the following —
(a) a State; or
(b) the Commonwealth;
licence holder means the holder of a GMO licence;
Ministerial Council means the Ministerial Council within the meaning of the Gene Technology Agreement;
notifiable low risk dealing has the meaning given by section 74;
officer, in relation to the Commonwealth, includes the following —
(a) a Minister of the Crown in right of the Commonwealth;
(b) a person who holds —
(i) an office established by or under a Commonwealth Act;
(ii) an appointment made under a Commonwealth Act; or
(iii) an appointment made by the Governor‑General or a Minister of the Crown in right of the Commonwealth but not under a Commonwealth Act;
(c) a person who is a member or officer of a Commonwealth authority;
(d) a person who is in the service or employment of the Commonwealth or of a Commonwealth authority, or is employed or engaged under a Commonwealth Act;
organism means any biological entity that is —
(a) viable;
(b) capable of reproduction; or
(c) capable of transferring genetic material;
person covered by a GMO licence means a person authorised by a GMO licence to deal with a GMO;
premises includes the following —
(a) a building;
(b) a place (including an area of land);
(c) a vehicle;
(d) a vessel;
(e) an aircraft;
(f) a facility;
(g) any part of premises (including premises referred to in paragraphs (a) to (f));
Record means the Record of GMO and GM Product Dealings mentioned in section 138 of the Commonwealth Act;
Regulator means the Gene Technology Regulator appointed under section 118 of the Commonwealth Act;
reviewable decision has the meaning given by section 179;
State includes the Australian Capital Territory and the Northern Territory;
State agency means —
(a) the Crown in right of Western Australia;
(b) a Minister of the Crown in right of Western Australia;
(c) an agency within the meaning of the Public Sector Management Act 1994;
(d) an instrumentality of the State of Western Australia, including a body corporate established for a public purpose by or under a law of the State of Western Australia; or
(e) a company in which a controlling interest is held by any one of the following persons, or by 2 or more of the following persons together —
(i) the Crown in right of Western Australia;
(ii) a person or body covered by paragraph (b) or (d);
(iii) a body covered by any of the above subparagraphs;
thing includes a substance, and a thing in electronic or magnetic form.
(2) If this Act requires or permits the Ministerial Council to do a thing, the Ministerial Council must do the thing in accordance with any requirements specified in the Gene Technology Agreement.
11. Meaning of intentional release of a GMO into the environment
For the purposes of this Act, a dealing with a GMO involves the intentional release of the GMO into the environment if the GMO is intentionally released into the open environment, whether or not it is released with provision for limiting the dissemination or persistence of the GMO or its genetic material in the environment.
12. Meaning of corresponding State law
Note for this section:
The Commonwealth Act includes a provision defining "corresponding State law" for the purposes of that Act.
12A. Meaning of reckless
(1) For the purposes of this Act a person is reckless with respect to circumstances if —
(a) the person is aware of a substantial risk that the circumstance exists or will exist; and
(b) having regard to the circumstances known to the person, it is unjustifiable to take the risk.
(2) For the purposes of this Act a person is reckless with respect to a result if —
(a) the person is aware of a substantial risk that the result will occur; and
(b) having regard to the circumstances known to the person, it is unjustifiable to take the risk.
(3) The question whether taking a risk is unjustifiable is one of fact.
Note for this section:
This section is not required in the Commonwealth Act.
Division 3 — Operation of Act
13. Operation of Act
Note for this section:
The Commonwealth Act includes a provision about the application of that Act.
14. Wind‑back of reach of Act
Note for this section:
The Commonwealth Act includes a provision about the giving of wind‑back notices by a State.
15. Relationship to other State laws
The provisions of this Act are in addition to, and not in substitution for, the requirements of any other law of Western Australia (whether passed or made before or after the commencement of this section).
Note for this section:
The equivalent section in the Commonwealth Act deals with the relationship of that Act to other Commonwealth laws.
Division 4 — Provisions to facilitate a nationally consistent scheme
Subdivision A — General provisions
16. State laws may operate concurrently
Note for this section:
The Commonwealth Act includes a provision allowing State laws (apart from State laws prescribed for the purposes of the provision) to operate concurrently with that Act.
17. Conferral of functions on Commonwealth officers and bodies
Note for this section:
The Commonwealth Act includes a provision allowing corresponding State laws to confer functions, powers and duties on certain Commonwealth officers and bodies.
18. No doubling‑up of liabilities
(1) If —
(a) an act or omission is an offence against this Act and is also an offence against the Commonwealth Act; and
(b) the offender has been punished for the offence under the Commonwealth Act,
the offender is not liable to be punished for the offence under this Act.
(2) If a person has been ordered to pay a pecuniary penalty under the Commonwealth Act, the person is not liable to a pecuniary penalty under this Act in respect of the same conduct.
19. Review of certain decisions
(1) Application may be made to the Administrative Appeals Tribunal for review of a reviewable decision.
(2) A decision made by the Regulator in the performance of a function or the exercise of a power conferred by this Act is a reviewable decision for the purposes of this section if —
(a) this Act provides for review by the Administrative Appeals Tribunal; and
(b) the decision is declared by the regulations made under the Commonwealth Act to be a reviewable State decision for the purposes of section 19 of the Commonwealth Act.
(3) The Administrative Appeals Tribunal Act 1975 of the Commonwealth (excluding Part IVA) and the regulations in force for the time being under that Act apply as laws of Western Australia in relation to reviewable decisions.
(4) For the purposes of this section, a reference in a provision of the Administrative Appeals Tribunal Act 1975 of the Commonwealth (as that provision applies as a law of Western Australia) to the whole or any part of Part IVA of that Act is taken to be a reference to the whole or any part of that Part as it has effect as a law of the Commonwealth.
Note for this section:
This section differs from section 19 of the Commonwealth Act.
20. Things done for multiple purposes
The validity of a licence, certificate or other thing issued, given or done for the purposes of this Act is not affected only because it was issued, given or done also for the purposes of the Commonwealth Act.
Subdivision B — Policy principles, policy guidelines and codes of practice
21. Ministerial Council may issue policy principles
(1) The Ministerial Council may issue policy principles in relation to the following —
(a) ethical issues relating to dealings with GMOs;
(aa) recognising areas, if any, designated under a law of Western Australia for the purpose of preserving the identity of one or both of the following —
(i) GM crops;
(ii) non‑GM crops,
for marketing purposes;
(b) matters relating to dealings with GMOs prescribed by the regulations for the purposes of this paragraph.
Notes for this subsection:
1. Section 57 provides that the Regulator must not issue a licence if to do so would be inconsistent with a policy principle.
2. Section 43 of the Interpretation Act 1984 confers power to revoke or amend any subsidiary legislation.
(2) Before issuing a policy principle, the Ministerial Council must be satisfied that the policy principle was developed in accordance with section 22 of the Commonwealth Act.
(3) Regulations for the purposes of subsection (1)(b) may relate to matters other than the health and safety of people or the environment, but must not derogate from the health and safety of people or the environment.
Note for this section:
This section differs from section 21 of the Commonwealth Act.
22. Consultation on policy principles
Note for this section:
The Commonwealth Act includes a provision about how policy principles are to be developed.
23. Ministerial Council may issue policy guidelines
The Ministerial Council may issue policy guidelines in relation to matters relevant to the functions of the Regulator under this Act or the regulations.
Notes for this section:
1. Section 56 requires the Regulator to have regard to policy guidelines when deciding an application for a GMO licence. Section 30 provides that the Regulator is not subject to direction in relation to individual decisions.
2. Section 43 of the Interpretation Act 1984 confers power to revoke or amend any subsidiary legislation.
24. Ministerial Council may issue codes of practice
The Ministerial Council may issue codes of practice, developed in accordance with section 24(2) of the Commonwealth Act, in relation to gene technology.
Notes for this section:
1. Section 43 of the Interpretation Act 1984 confers power to revoke or amend any subsidiary legislation.
2. Section 24 of the Commonwealth Act includes provisions about how codes of practice are to be developed and making them disallowable instruments.
Part 3 — The Gene Technology Regulator
25. Simplified outline
In outline this Part specifies the functions and powers of the Gene Technology Regulator under this Act or the regulations.
Note for this section:
This section differs from section 25 of the Commonwealth Act.
26. The Gene Technology Regulator
Note for this section:
Section 26 of the Commonwealth Act creates the office of Gene Technology Regulator.
27. Functions of the Regulator
The Regulator has the following functions —
(a) to perform functions in relation to GMO licences as set out in Part 5;
(b) to develop draft policy principles and policy guidelines, as requested by the Ministerial Council;
(c) to develop codes of practice;
(d) to issue technical and procedural guidelines in relation to GMOs;
(e) to provide information and advice to other regulatory agencies about GMOs and GM products;
(f) to provide information and advice to the public about the regulation of GMOs;
(g) to provide advice to the Ministerial Council about —
(i) the operations of the Regulator and the Gene Technology Technical Advisory Committee; and
(ii) the effectiveness of the legislative framework for the regulation of GMOs, including in relation to possible amendments of relevant legislation;
(h) to undertake or commission research in relation to risk assessment and the biosafety of GMOs;
(i) to promote the harmonisation of risk assessments relating to GMOs and GM products by regulatory agencies;
(j) to monitor international practice in relation to the regulation of GMOs;
(k)
