Radiocommunications (Compliance Labelling — Electromagnetic Radiation) Notice 2003
The AUSTRALIAN COMMUNICATIONS AUTHORITY makes this Notice under section 182 of the Radiocommunications Act 1992.
Dated    27 February	 2003
A.J SHAW                                                                                                                 Chair
R HORTON                                                                                                             Deputy Chair
Australian Communications Authority

Contents
Part 1	Preliminary
	1	Name of Notice	3
	2	Commencement	3
	3	Revocation	3
	4	Definitions	3
	5	Category A devices	6
	6	Transitional	6
	7	Application of this Notice to devices	7
	8	Relationship between this Notice and the Telecommunications Labelling (Customer Equipment and Customer Cabling) Notice 2001	7
Part 2	Requirements to be met before a label may be applied
Division 2.1	Application of Part 2
	9	No application to variants of a device	8
Division 2.2	Permission to use regulatory marks and issue supplier code numbers
	10	Notification	8
	11	Declaration of conformity	9
Division 2.3	Compliance levels
	12	Compliance levels	9
	13	Compliance level 1	9
	14	Compliance level 2	10
	15	Compliance level 3	10
Division 2.4	Assessment of devices
	16	Assessment	10
Part 3	Form and placement of a compliance label
	17	Application of Part 3	11
	18	Who must apply a compliance label to a device	11
	19	What is a compliance label	11
Part 4	Requirements to be met after labels applied
Division 4.1	Keeping of records
	20	Compliance records	13
	21	Keeping of records — general requirements	13
	22	Records of testing for category B devices	13
Division 4.2	Availability of compliance records for inspection
	23	Where compliance records are to be available	14
	24	Provision of information to authorised officer	14
	25	Testing of items by testing body	14
Schedule 1	Labels	16
Part 1	The labels	16
Part 2	The Marks	16
Schedule 2	Supplier’s Declaration of Conformity	18
Schedule 3	Notification and Application to use C‑Tick mark	18

Part 1	Preliminary
  
1	Name of Notice
		This Notice is the Radiocommunications (Compliance Labelling — Electromagnetic Radiation) Notice 2003.
2	Commencement
		This Notice commences on 1 March 2003.
3	Revocation
		The Radiocommunications (Compliance Labelling — Electromagnetic Radiation) Notice 2001 is revoked.
4	Definitions
	(1)	In this Notice:
accredited testing body means a laboratory that is described in subsection (2) or (3).
Act means the Radiocommunications Act 1992.
agent, of a manufacturer or importer, means a person who is authorised in writing by the manufacturer or importer to act in Australia as an agent of the manufacturer or importer for Division 7 of Part 4.1 of the Act.
applicable standard means the Radiocommunications (Electromagnetic Radiation — Human Exposure) Standard 2003, as in force from time to time.
ARPANSA standard means the Radiation Protection Standard for Maximum Exposure Levels to Radiofrequency Fields – 3 kHz to 300 GHz published by the Australian Radiation Protection and Nuclear Safety Agency and assigned the number ISBN 0-0642-79400-6.
Note   The ARPANSA standard may be obtained from the Australian Radiation Protection and Nuclear Safety Agency website http://www.arpansa.gov.au .
AS 2772.2 means the Australian Standard Radiofrequency radiation Part 2: Principles and methods of measurement – 300 kHz to 100 GHz (AS 2772.2) published by Standards Australia.
aware user device means a hand‑held or body‑worn radiocommunications transmitter that operates on a push‑to‑talk basis and is intended for use as:
	(a)	an ambulatory station; or 
	(b)	a land mobile system station; or
	(c)	a maritime ship station; or
	(d)	a citizens band radio station; or
	(e)	an amateur station.
authorised officer means:
	(a)	an inspector under subsection 267 (1) of the Act; or
	(b)	a person authorised in writing by the ACA for sections 24 and 25.
category A device has the meaning given by section 5.
category B device means a device that is not a category A device.
compliance label has the meaning given by subsection 19 (1).
Note   Section 8 extends some references to ‘compliance label’ in this Notice to include a compliance label under the Telecommunications Labelling (Customer Equipment and Customer Cabling) Notice 2001.
compliance mark means any of the marks in Part 2 of Schedule 1.
compliance record has the meaning given by section 20.
C-Tick mark means the mark set out in Part 2 of Schedule 1.
declaration of conformity means a declaration that:
	(a)	is in the form set out in Schedule 2; or
	(b)	contains the information required in the form set out in Schedule 2, whether or not the declaration is accompanied by other material.
Note   Suppliers are not required to copy the declaration set out in Schedule 2. They may create their own forms, which contain, as a minimum, the information mentioned in Schedule 2.
description of the device means sufficient information for a person to determine whether the device is the same as a device for which a declaration of conformity, test report or assessment against the applicable standard was prepared.
Note   The description of a device may include a photograph or sketch or other pictorial representation of the device illustrating its internal and external aspects (including printed circuit boards).
device means a mobile station to which the applicable standard applies.
human body means the head, neck and trunk but not the limbs.
mobile station means a transmitter that is established for use:
	(a)	in motion, on land, water or in the air; or
	(b)	in a stationary position at unspecified points on land, water or in the air.
Examples of a mobile station
1   A wireless modem operating in a laptop computer.
2   A hand-held cellular or PCS telephone with a radiating antenna in the handpiece.
NATA means the National Association of Testing Authorities, Australia (ACN 004 379 748).
non-aware user device means a device other than an aware user device.
normal position of use, of a device, means:
	(a)	the position specified in the measurement method applicable to the device in section 10, 11 or 12 of the applicable standard; or
	(b)	if paragraph (a) does not apply, the common use spatial orientation of the device with respect to the user; or
	(c)	if paragraphs (a) and (b) do not apply, the spatial orientation of the device with respect to the user defined by the manufacturer.
product identification code, for a device, means the written information used by the supplier of the device to identify the device.
RCM means the Regulatory Compliance Mark set out in Part 2 of Schedule 1.
Note   The RCM is reproduced from the Appendix to AS/NZS 4417.
Specific Absorption Rate, or SAR, means the rate at which RF energy is absorbed in body tissues, expressed as watts per kilogram (‘W/kg’).
supplier means:
	(a)	in relation to an imported device — the importer or agent of the importer; and
	(b)	in relation to a device manufactured in Australia — the manufacturer or the agent of the manufacturer.
supplier code number means a code number issued to a person: 
	(a)	in accordance with a notice made by the ACA under section 407 of the Telecommunications Act 1997; or
	(b)	in accordance with a notice made by the ACA under section 182 of the Act; or
	(c)	by Standards Australia International Limited under AS/NZS 4417.
variant means a version of a device that is not identical to the device but is not sufficiently different from the device to affect the application to that version of a standard that applies to the device.
working day, in relation to a request, means a day other than:
	(a)	a Saturday or a Sunday; or
	(b)	a day that is a public holiday or an Australian Public Service holiday in the place where the request is made.
	(2)	Before 1 March 2005, an accredited testing body is a laboratory that is:
	(a)	accredited by:
	(i)	NATA; or
	(ii)	an accreditation body of a foreign country, being a body with whom NATA has a mutual recognition arrangement or agreement; 
		to conduct tests for specific absorption rate; or
	(b)	certified in accordance with International Standards Organisation ISO 9001:2000, as in force from time to time; or
	(c)	accredited, in accordance with International Standards Organisation ISO 17025, as in force from time to time, to test the specific absorption rate.
	(3)	On and after 1 March 2005, an accredited testing body is a laboratory that is accredited by:
	(a)	NATA; or
	(b)	an accreditation body of a foreign country, being a body with whom NATA has a mutual recognition arrangement or agreement; 
to conduct tests for specific absorption rate.
Note   On and from 1 March 2005, category B devices whose normal position of use is not more than 20cm from the human body must have tests for specific absorption rate conducted only by the bodies mentioned in subsection (3).
	(4)	A reference in this Notice to a document with the prefix ‘AS/NZS’ is a reference to a document that is a joint Australian and New Zealand Standard approved for publication on behalf of the Standards organisations of those countries, as in force from time to time.
	(5)	Reference may be made in this Notice to an Australian and New Zealand Standard by number alone without inclusion of the edition or year of publication of the standard.
Example
AS/NZS 4417.1:1996 may be referred to as AS/NZS 4417.1.
	(6)	A term that is:
	(a)	used (but not defined) in this Notice; and
	(b)	defined in the Glossary of the ARPANSA standard;
has the meaning given by the Glossary.
5	Category A devices
	(1)	A category A device is a device that meets the criteria in subsection (2) or (3).
	(2)	The criteria in this subsection are that the device:
	(a)	is an aware user device; and
	(b)	is not required to be evaluated under section 5.2 of Schedule 5 to the ARPANSA Standard.
	(3)	The criteria in this subsection are that the device:
	(a)	is a non-aware user device; and
	(b)	is not required to be evaluated under section 5.3 of Schedule 5 to the ARPANSA standard.
6	Transitional
	(1)	The Radiocommunications (Compliance Labelling — Electromagnetic Radiation) Notice 2001, as in force immediately before 1 March 2003, continues to apply to a radiocommunications device to which the old standard applies under section 7 of the Radiocommunications (Electromagnetic Radiation — Human Exposure) Standard 2003.
	(2)	Subsection (1) ceases to apply at the end of 29 February 2004.
7	Application of this Notice to devices
	(1)	This Notice applies to a device if:
	(a)	the device is manufactured in Australia, or imported, for supply; and
	(b)	the applicable standard applies to it.
	(2)	This Notice does not apply to a device that is imported or manufactured otherwise than for supply in Australia.
	(3)	This Notice does not apply to a category B device for which there is no applicable measurement method under the applicable standard.
8	Relationship between this Notice and the Telecommunications Labelling (Customer Equipment and Customer Cabling) Notice 2001
		If a device to which this Notice applies is also customer equipment or customer cabling to which the Telecommunications Labelling (Customer Equipment and Customer Cabling) Notice 2001, as in force from time to time, applies:
	(a)	the requirements in this Notice are additional to the requirements under that Notice; and
	(b)	Part 3 of this Notice does not apply in relation to the device; and
	(c)	a reference in this Notice (except subsection 4 (1)) to a compliance label includes a reference to a compliance label under that Notice.
Note   An effect of paragraph (b) is that the supplier of a device that is to be labelled with an A-Tick under the Telecommunications Labelling (Customer Equipment and Customer Cabling) Notice 2001 is not required to label the device with a C-Tick as well.
Part 2	Requirements to be met before a label may be applied
Division 2.1	Application of Part 2
9	No application to variants of a device
		This Part does not apply in relation to a variant of a device if:
	(a)	the relevant requirements of this Part have been met in relation to the device; and
	(b)	the electromagnetic radiation exposure in relation to the variant is not likely to exceed that of the device.
Division 2.2	Permission to use regulatory marks and issue supplier code numbers
10	Notification
	(1)	Before a supplier applies a label with a C-Tick mark to a device as a compliance label for the first time, the supplier must have obtained from the ACA:
	(a)	permission to use the C-Tick mark as part of the label; and
	(b)	a supplier code number.
	(2)	An application for permission and the supplier code number must be:
	(a)	in the form set out in Schedule 3; or
	(b)	in writing setting out the information required in the form set out in Schedule 3, whether or not the application is accompanied by other material.
Note   Suppliers are not required to copy Schedule 3. They may create and submit their own forms, which must contain as a minimum the information mentioned in Schedule 3.
	(3)	Before a supplier applies a label with the RCM to a device as a compliance label for the first time, the supplier must register the supplier’s use of the RCM with the ACA in accordance with clause 4.6 of AS/NZS 4417.1, as if references in that Standard to the Spectrum Management Agency and SMA were references to the ACA.
	(4)	This section does not apply if the ACA has previously issued the supplier with a supplier code number and:
	(a)	an approval to use a mark under the Telecommunications Labelling (Customer Equipment and Customer Cabling) Notice 2001, as in force from time to time; or
	(b)	an approval to use a mark under the Radiocommunications Devices (Compliance Labelling) Notice 1996, as in force from time to time.
11	Declaration of conformity
	(1)	Before a supplier of a device applies a label to the device as a compliance label, the supplier must make a declaration of conformity for the device.
	(2)	Subsection (1) is taken to be satisfied by an importer of a device, or an agent of the importer, who applies a label to the device as a compliance label without making a declaration of conformity for the device if:
	(a)	the device complies with the applicable standard; and
	(b)	the device was manufactured outside Australia; and
	(c)	the manufacturer of the device made a declaration of conformity for the device before the label was applied to the device.
	(3)	A reference to manufacturer in a declaration of conformity made in accordance with paragraph (2) (c) is taken to include a reference to a person who manufactures a device outside Australia.
	(4)	A manufacturer that manufactures a device outside Australia and made a declaration of conformity in accordance with paragraph (2) (c) need not provide:
	(a)	a supplier code number; or
	(b)	an Australian Business Number (ABN); or
	(c)	an Australian Company Number (ACN); or
	(d)	an Australian Registered Body Number (ARBN).
Division 2.3	Compliance levels
12	Compliance levels
	(1)	Before a supplier applies a compliance label to a device, the supplier must comply with the compliance level for the device.
	(2)	The compliance level for a device is:
	(a)	for a category A device — compliance level 1; and
	(b)	for a category B device for which the normal position of use is more than 20cm from the human body — compliance level 2; and
	(c)	for a category B device for which the normal position of use is not more than 20cm from the human body — compliance level 3.
13	Compliance level 1
		To comply with compliance level 1, the supplier of a device must:
	(a)	prepare a description of the device; and
	(b)	make a declaration of conformity for the device in accordance with section 11.
Note   Subsection 11 (2) sets out the circumstances in which the requirement for a supplier of a device to make a declaration of conformity is taken to be satisfied by the overseas manufacturer of the device making the declaration.
14	Compliance level 2
		To comply with compliance level 2, the supplier of a device must:
	(a)	comply with compliance level 1; and
	(b)	show conformity with the applicable standard by a report of the results of assessment under section 16.
15	Compliance level 3
		To comply with compliance level 3, the supplier of a device must:
	(a)	comply with compliance level 1; and
	(b)	show conformity with the applicable standard by a report of the results of assessments under section 16 by an accredited testing authority.
Division 2.4	Assessment of devices
16	Assessment 
		If a device is assessed for conformity with the applicable standard, the supplier of the device must obtain from the person that assessed the device a report addressing:
	(a)	the measurements or evaluation methods that were used; and
	(b)	the results of the measurements or evaluations, including any measurement or evaluation data; and
	(c)	whether the results of the measurements or evaluations show that the device meets the applicable standard.
Part 3	Form and placement of a compliance label
  
17	Application of Part 3
	(1)	This Part applies to a device if the supplier for the device has complied with the compliance level for the device under Part 2.
	(2)	This Part also applies to a variant of the device.
18	Who must apply a compliance label to a device
	(1)	If a device is manufactured in Australia, a label must be applied to the device as a compliance label by 1 of the following persons:
	(a)	the manufacturer; 
	(b)	an agent of the manufacturer; 
	(c)	a person who is authorised by the manufacturer, or an agent of the manufacturer, to apply labels on behalf of the manufacturer or agent.
Note   A compliance label is described in subsection 19 (1).
	(2)	If a device is manufactured outside Australia, a label must be applied to the device as a compliance label by 1 of the following persons:
	(a)	the importer; 
	(b)	an agent of the importer; 
	(c)	a person outside Australia who is authorised by the importer or agent to apply labels on behalf of the importer or agent.
19	What is a compliance label
	(1)	A compliance label for a device is a label that meets the requirements of this section.
	(2)	The label must be in the form set out in Part 1 of Schedule 1.
	(3)	The label must include the information specified in at least 1 of the paragraphs in subsection (4) about:
	(a)	in relation to an imported device — the importer; and
	(b)	in relation to a device manufactured in Australia — the manufacturer.
	(4)	The information is the following:
	(a)	business name and business address in Australia;
	(b)	business name registered on the national business names register within the meaning of section 147 of the Corporations Act 2001;
	(c)	personal name and address of place of business in Australia;
	(d)	Australian Company Number or ACN under section 118 of the Corporations Act 2001;
	(e)	Australian Registered Body Number or ARBN under Part 5B.2 of the Corporations Act 2001;
	(f)	Australian Business Number under the A New Tax System (Australian Business Number) Act 1999;
	(g)	registered trade mark under the Trade Marks Act 1995;
	(h)	supplier code number issued by the ACA, or in respect of the RCM, by Standards Australia International Limited.
	(5)	Subject to subsections (6) and (7), the label must be:
	(a)	legible with alphanumeric characters of at least 1 mm high and the compliance mark at least 3 mm high; and
	(b)	made of durable material; and
	(c)	applied to the device:
	(i)	permanently; or
	(ii)	in a way that would make it difficult to obliterate or remove the label; and
	(d)	applied:
	(i)	to the external surface of the device; and
	(ii)	if the external surface of the device displays the product identification code for the device, as near as practicable to that code.
	(6)	If it is not possible to apply the label to the external surface of the device because of the size or physical nature of the device, the label must be applied to the labelling or outer surface of the packaging associated with the device.
	(7)	If it is possible, but not practical, to apply the label to the external surface of the device, the label must be applied to 1 of the following items associated with the device (listed in order of priority):
	(a)	the outer surface of the packaging; 
	(b)	the instructions for use; 
	(c)	the warranty or guarantee certificates.
	(8)	Before applying a label under subsection (7), the supplier must:
	(a)	apply in writing to the ACA for approval to apply the label, setting out the reasons why subsection (7) should apply; and
	(b)	tell the ACA about the intended placement of the label; and
	(c)	obtain written approval from the ACA to apply the label.
Part 4	Requirements to be met after labels applied
Division 4.1	Keeping of records
20	Compliance records
		A compliance record is a record that must be kept under section 21.
21	Keeping of records — general requirements
	(1)	If a supplier of a device applies a label to the device as a compliance label, the supplier must keep, for 5 years after the device has ceased to be supplied in Australia:
	(a)	the declaration of conformity relating to the device; and
	(b)	the description of the device; and
	(c)	for a category B device — the records mentioned in section 22; and
	(d)	for a device to which a label is applied under subsection 19 (7) — records of the documents and information mentioned in subsection 19 (8).
	(2)	If an agent of a manufacturer or importer keeps records for the manufacturer or importer that must be kept under subsection (1), the agent must also keep a copy of its agency agreement with the manufacturer or importer for the same period as those records are kept.
	(3)	A compliance record:
	(a)	must be in English; and
	(b)	may be a copy of an original record; and
	(c)	may be kept in electronic form.
22	Records of testing for category B devices
		For paragraph 21 (1) (c), the records are:
	(a)	the report issued under section 16 showing that the device meets the applicable standard; and
	(b)	for a variant — a statement by the supplier that:
	(i)	identifies the device and its variant; and
	(ii)	describes the differences between the device and its variant; and
	(iii)	provides a technical rationale for the conformity of the variant; and
	(iv)	includes evidence that the electromagnetic radiation exposure in relation to the variant is not likely to exceed that of the device.
Division 4.2	Availability of compliance records for inspection
23	Where compliance records are to be available
		If a supplier of a device applies a label to the device as a compliance label, the supplier must ensure that the compliance records for the device are available at the principal business address in Australia of the supplier.
24	Provision of information to authorised officer
	(1)	If a supplier of a device applies a label to the device as a compliance label, an authorised officer, may in writing, require the supplier to give to the officer specified compliance records.
	(2)	If the request is for a specified record, the supplier must produce the record within 10 working days after the day specified in the request.
	(3)	If the request is for a specified circuit diagram or manual for the device, the supplier must produce the document within 30 working days after the day specified in the request.
	(4)	After receiving the information from the supplier, the authorised officer must give the supplier a receipt for the information supplied.
	(5)	The authorised officer:
	(a)	may make copies of the records; and
	(b)	must return the records given by the supplier as soon as practicable and, in any case, not more than 60 days after receiving the records.
	(6)	If an authorised officer believes that the records kept by the supplier do not provide sufficient evidence that the device complies with the applicable standard, the officer may, in writing, require the supplier to give to the officer a test report from an accredited testing body showing that the device either complies or does not comply with the applicable standard.
25	Testing of items by testing body
	(1)	If a supplier of a device applies a label to the device as a compliance label, an authorised officer may, in writing, require the supplier of a device to give up to 3 samples of the device to a laboratory accredited by NATA and specified by the officer, for testing whether the device complies with an applicable standard.
	(2)	The supplier must comply with the request within 10 working days after the day specified in the request.
	(3)	The supplier must attempt to obtain from the laboratory a receipt that specifies the samples have been received and the date when they were received.
	(4)	On receiving a request from the ACA, the supplier must:
	(a)	give the receipt to the ACA; or
	(b)	if the supplier is unable to obtain a receipt — satisfy the ACA that the supplier made reasonable attempts to obtain a receipt.
	(5)	The ACA must make arrangements to ensure that the samples are returned to the supplier within a reasonable period after they have been tested.
	(6)	If testing required under section 25 shows that the device does not comply with the standard, the supplier must meet the financial costs of the testing.
	(7)	If testing required under section 25 shows that the device complies with the standard, the ACA must meet the financial costs of the testing.
	(8)	In this section:
device includes a variant of the device.

Schedule 1	Labels
(subsections 4 (1) and 19 (2))

Part 1	The labels

Either the C-tick mark or the RCM	Information required under subsection 19 (3)	

Part 2	The Marks
The C-Tick mark

Note   The C-Tick mark is a protected symbol for section 188A of the Radiocommunications Act 1992.

The RCM

Note   The RCM is a trademark owned by Australian and New Zealand regulators.  Manufacturers or importers who intend to use the RCM should register with Standards Australia International Limited in accordance with AS/NZS 4417.1.
Schedule 2	Supplier’s Declaration of Conformity
(subsection 4 (1))

			
Supplier’s Declaration of Conformity

As required by Notices under:
•	section 182 of the Radiocommunications Act 1992;
•	section 407 of the Telecommunications Act 1997.

INSTRUCTIONS FOR COMPLETION

This completed form remains with the supplier as part of the documentation required for the compliance records.  Do not return to the ACA.

SUPPLIER’S DETAILS
Name of Manufacturer, Importer or Agent		ACA Supplier Code Number, or	

		Australian Business Number (ABN), or	
Address of Manufacturer, Importer or Agent														
														
		Australian Company Number (ACN), or	

		Australian Registered Body Number (ARBN)	

PRODUCT DETAILS

Product Name, Type and Model

	

	

APPLICABLE STANDARDS

Standard Title, Number and if applicable the Test Report Number

	

	

	

DECLARATION

I hereby declare that the product mentioned above complies with the above mentioned standards and all products supplied under this Declaration will be identical to the sample identified above.		Signature of Authorised Person		Date	

							
		Print Name	

		Position in Organisation	

Schedule 3	Notification and Application to use C‑Tick mark
(subsection 10 (2))
			
Application to use the C-Tick mark

Instructions for Completion: 	
Please print clearly.  Illegible, unclear or incomplete application forms may delay processing.  
Send completed forms by mail or fax to:-
Your nearest ACA Regional Office				
(See reverse for contact details)		
	
Supplier (i.e., manufacturer, importer or an authorised agent) Details:	
Name of company (or partnership, trading trust or individual)		Australian Company Number (ACN), or 
Australian Registered Body Number (ARBN), or 
Australian Business Number (ABN)	

Postal address		Street address (if same as postal address, write ‘as above’)	
			
	              Postcode			                Postcode	
Contact numbers			
Phone (             )		Fax (             )	
Mobile (             )		Email 	
Street address where compliance records are accessible (if same as postal address, write ‘same as postal address’)	
	                          Postcode	
	
Declaration:	
I advise that it is our intention to market electrical and electronic devices in Australia under the C-Tick mark.  
I understand that products marked with the C-Tick mark may only be marketed where a complete Declaration of Conformity relating to the products has been made and there are adequate technical grounds for making a Declaration of Conformity in the form of a test report or Technical Construction File. 		Signature of supplier / agent 	Date	
				
		Name (Print)	
			
		Position in Organisation	
			
For your information	
It is an offence to make a false statement in connection with the operation of the Radiocommunications Act 1992.
Penalty: 100 penalty units.	

	ACA Regional Offices	

New South Wales Region (including Canberra, Newcastle and Coffs Harbour Operations Centres)

	Regional Office
	GPO Box 5295
	SYDNEY NSW 2001
	
	Facsimile: (02) 9245 4099

Southern Australia Region (including Adelaide, Hobart and Wodonga Operations Centres)

	Regional Office
	PO Box 13120 
	MELBOURNE VIC 8010

	Facsimile: (03) 9963 6989

Northern Australia Region (including Darwin and Townsville Operations Centres)

	Regional Office
	PO Box 1225
	CAIRNS QLD 4870
	
	Facsimile: (07) 4048 7400

Southern Queensland Region (including Rockhampton Operations Centre)

	Regional Office
	PO Box 288
	RED HILL QLD 4059
	
	Facsimile: (07) 3247 7100
		
Western Australia Region

	Regional Office
	PO Box 6189
	EAST PERTH WA 6892
	
	Facsimile: (08) 9461 2100