Australian EMC Regulation and Routes
to Compliance
The C-tick scheme is standards based
and reliant on self-declaration of
conformity by equipment suppliers.
On
January 1, 1997, EMC compliance with national
emission standards derived from CISPR
standards became mandatory for electrical
equipment marketed in Australia. The Australian
Communications Authority (ACA) later,
in 1998, clarified the scope and application
of the EMC regulations. Compliance with
the revised regulations is by means of
self-declaration, and suppliers must ensure
that the products they are placing on
the Australian market meet the relevant
EMC standards. New Zealand's EMC regulations
are similar to Australia's but contain
small differences. Negotiated harmonization
is expected soon to bring about transparency
between the two countries. The Australian
EMC framework displays similarities to
both the European EMC Directive and the
FCC Part 15 Rules.
This article outlines the EMC
regulations in Australia and the available
routes to compliance. It details the scope
of the regulations, the applicable standards,
and the compliance requirements for various
product categories. The testing and technical
construction file routes to compliance are
explained, as are labeling requirements
and enforcement mechanisms.
Overview of Australian EMC Regulations
In July 1997 the Spectrum Management
Agency and Austel merged to form the ACA,
the single regulatory body now responsible
for administering product compliance regulations
in the areas of EMC, radiocommunications,
and telecommunications. The ACA has moved
away from the premarket approval approach
to a scheme that features minimal regulator
responsibility for the approval of products.
The new self-declaration scheme facilitates
efficient and unimpeded access to the
Australian market, without the processing
delays and filing fees prevalent under
traditional premarket approval systems.
It does, however, place primary responsibility
for product compliance directly on the
supplier.
On January 1, 1997, compliance with the
appropriate emission standards became
mandatory for all equipment marketed for
the first time for use in the commercial,
light industrial, and residential environments.
Products on the market prior to that date
had until January 1, 1999, to be made
compliant. On November 11, 1998, the legal
instruments were changed in order to clarify
the scope of the new regulatory scheme
and to support its practical implementation.
The new regulation mandated EMC standards
without reference to the particular use
environments, thus removing the problems
associated with the previous regulation's
specification of EMC environments (light
industrial, heavy industrial, and so on).
This made implementation of the EMC regulations
easier by shifting the focus from the
specification of particular products and
environments to the applicability of the
scope of some individual EMC standard.
If a product comes under the scope of
one of the mandated EMC standards and
it is not specifically excluded from the
EMC framework, it must comply.
Compliance with the EMC regulations requires
that the supplier placing the product
on the Australian market declare that
the product meets the applicable EMC standards.
The declaration is to be supported by
a compliance folder including test data
or other evidence to support the claims
of compliance. The product must be labeled
with the C-tick mark and other information
that is used to trace the supplier. Permission
to use the C-tick mark must be obtained
from the ACA before a supplier can legally
apply it. Permission, granted in the form
of a supplier code, is available only
to residents of Australia. The ACA will
recognize agents authorized by manufacturers
in cases where the resident agent accepts
the responsibility for compliance. The
ACA supplier code, or other information
that makes the identity of the supplier
evident, must be used in conjunction with
the C-tick on all products marketed by
a supplier. The ACA uses this information
to trace the responsible supplier if the
compliance of a device is called into
question or in the event of an audit.
Mandatory EMC Standards. The ACA
has addressed the problem of electromagnetic
interference by implementing a standards-based
regulation. All electrical and electronic
products that fall within the scope of
one of the mandated standards of the EMC
framework, and that are not covered by
the exemption provisions, must comply
with the regulations. There are no mandatory
immunity requirements except for medical
equipment covered by the Therapeutic Goods
Administration (TGA).
The Australian EMC standards are derived
from the internationally harmonized CISPR
standards and are generally adopted by
Standards Australia and Standards New
Zealand as harmonized Australian/New Zealand
standards (AS/NZS), sometimes with minor
national deviations. In some cases, interpretations
and variations in implementation of the
standards may conflict with the requirements
of other regulatory regimes, such as the
FCC and the European EMC Directive. Retesting
or "top-up" testing of products approved
elsewhere may sometimes be necessary to
ensure that the product has been fully
tested to the Australian variations and
at the Australian mains voltage of 240
V ac at 50 Hz.
The ACA mandatory standards (with their
international source standards in parentheses)
are
-
AS/NZS 3548 (CISPR 22/EN 55022):
Information technology equipment (ITE).
-
AS/NZS 2064 (CISPR 11/EN 55011):
Industrial scientific and medical (ISM)
equipment.
-
AS/NZS 2557 (CISPR 12): Spark
ignition equipment.
-
AS/NZS 1053 (CISPR 13/EN 55013):
TV, radio receivers.
-
AS/NZS 1044 (CISPR 14/EN 55014):
Domestic and household appliances.
-
AS/NZS 4051 (CISPR 15/EN 55015):
Luminaires and lighting equipment.
-
AS/NZS 1052 (CISPR 16/EN 55016):
Measurement methods and apparatus.
-
AS/NZS 4251.1 (IEC 61000-6-3):
Generic emission standard, light industry.
-
AS/NZS 3652 (EN 50199:1996):
Arc welding equipment (emissions only).
It is important to note that not all
EMC standards published as AS/NZS standards
are mandated by the ACA into regulation.
A product must comply with the EMC standard
applicable at the time the product enters
the market for the first time. If the
particular EMC standard was modified within
six months of the product's introduction
to the market, then the previous version
of the standard may be used. The standard
applicable at the time the product is
first marketed is applicable for the life
of the product. There is no set date for
withdrawal of superseded standards as
is the case with the European EMC Directive.
Whenever the product is modified, the
new (current) standard applies.
Exemptions. Equipment that falls
within the scope of other regulatory bodies
is exempt from the ACA EMC regulations.
The Civil Aviation Safety Authority approves
equipment fitted to aircraft. Equipment
used by defense forces for military operations
is under the purview of the Australian
Department of Defense. The Department
of Transport and Regional Services regulates
design safety codes for road-registrable
vehicles. EMC requirements modeled on
the European Automotive Directive have
been adopted by the Federal Chamber of
Automotive Industries. However, aftermarket
products intended for automotive applications
are subject to the full provisions of
the EMC regulations. And, lastly, all
medical devices covered by the listing
requirements of the TGA are exempt from
the ACA EMC regulations.
In general, equipment that falls under
the scope of one of the mandated standards
must comply unless it meets the exclusion
criteria. Categories of products receiving
general exclusion from the EMC regulations
include
-
Devices for export.
-
Prototypes and equipment on
display at exhibitions and trade fairs.
-
Kits sold to hobbyists.
-
Spare parts.
-
Secondhand apparatus (except
imported secondhand devices, which are
deemed to be new).
-
Electromagnetically benign
devices (those that emit a total interference
power of less than 6 nW).
-
Inputs to other devices (an
exclusion generally intended for components
and not OEM devices).
-
Equipment specifically for
rental or lease purposes. (If subsequently
sold, compliance becomes mandatory.
This exemption is likely to be removed
in the near future.)
-
Amateur radio equipment and
other devices subject to ACA radiocommunications
licenses and type approvals.
-
Devices used for the study
of electromagnetic effects in an educational,
training, or research institution.
-
Specific installations excluded
by the ACA.
-
Installations.
Other exemptions have come into existence
as a result of legal interpretation of
the CISPR standards.
The EMC regulation has modified the scope
of some standards so that some equipment
is intentionally exempted from the compliance
requirements. Equipment powered by three-phase
mains supply, or by battery, and being
governed by AS/NZS 1044 (CISPR 14) or
AS/NZS 4051 (CISPR 15) is exempted from
the EMC regulations (that is, only single-phase
equipment under these standards must comply).
The intention of this exemption was to
exclude industrial machines and simple
battery-operated devices, such as toys
and domestic appliances. Another special-case
exemption involves the generic emission
standard, AS/NZS 4251.1 (EN 50081-1/IEC
61000-6-3). In general, products not covered
by the scope of a family standard or a
product-specific standard are covered
by the generic standard. According to
legal advice received by the ACA, battery-operated
equipment does not fall under the scope
of the generic emission standard; hence,
it is exempt from the regulations.
Declaration of Conformity.
The Australian regulations are based on
the manufacturer's declaration of conformity
(DoC). Once compliance is established, and
prior to marketing, a DoC with a sound and
justifiable basis is prepared. The DoC is
placed in a compliance folder, and the C-tick
is then affixed to the product. At this
stage there is no need to submit products
or any documentation to the ACA for testing
or certification. A test report accredited
by NATA (National Assocation of Testing
Authorities, Australia) has national and
international recognition. The ACA will
always be satisfied with a bona fide NATA
report or one produced by a mutual recognition
agreement (MRA) partner.
Although the previous system of
Austel permits has been changed to a DoC
system, NATA- or MRA-accredited testing
remains compulsory. All devices connecting
to the telecommunications system must be
tested for compliance to the appropriate
limit under AS/NZS 3548. As of January 1,
1998, Class A limits apply to all devices
to be used in a commercial or industrial
environment, and Class B limits apply to
devices used in a domestic or residential
environment. There are some differences
in the compliance and marking requirements
for telecommunications and terminal equipment
(TTE), which are covered under the "Labelling
Instrument" section of the Telecommunications
Act 1997. The C-tick is not used for TTE
devices. The A-tick must be applied once
the additional requirements of the labeling
notice have been met.
Items of equipment covered under AS/NZS
2064 (CISPR 11) as Group 2 ISM devices
are considered high risk and must be declared
only on the basis of a NATA or NATA MRA
partnerendorsed report.
The C-tick Mark. Use of
the C-tick mark is regulated under a legal
instrument issued in September 1998, under
Subsection 183 of the Radiocommunications
Act 1992, "Radiocommunications (C-Tick
Mark) Determination 1998," which established
the design of the C-tick mark and specified
it as a protected symbol under the regulations.
The determination regulates the use and
application of the C-tick mark for products
under the scope of the Radiocommunications
Act, including products subject to the
EMC requirements. It is an offense to
use the C-tick mark without first registering
as a supplier or to use it on products
that are not covered by the EMC regulations.
The C-tick mark may be used in advertising,
packaging, displays, warranties, and user
instructions to indicate that a product
complies with applicable standards. It
may also
Compliance Levels. The Australian
EMC regulation defines three levels of
compliance requirements based on the expected
risk of interference to radiocommunications
and telecommunications arising from use
of the product.
Compliance Level 1. Level 1 covers
low-risk devices that are unlikely to
generate emissions with the potential
to cause interference. Examples are low-EMI-risk
squirrel-cage motors, simple relays, and
basic ac-to-ac transformers. Conformance
assessment procedures are not mandatory,
and the C-tick can be applied without
necessarily performing formal testing.
Responsibility for proof of compliance,
however, still rests with the supplier,
who must sign a DoC, establish a compliance
folder, and apply the C-tick.
Compliance Level 2. Level 2 devices
are those not qualifying for Level 1 (low
risk) or Level 3 (high risk). They are
considered to have medium potential to
cause interference. Level 2 devices include
most of the electrical devices covered
by the mandated (CISPR) standards except
for high-risk TTE devices covered by AS/NZS
3548 (CISPR 22) and Group 2 ISM products
within the scope of AS/NZS 2064 (CISPR
11). While NATA or MRA reports are not
mandatory, the ACA views provision of
a test report from a laboratory accredited
for the particular standard as constituting
a high-confidence, low-risk approach to
compliance. If the compliance of the product
should be challenged, the ACA will request
the testing of three samples by a NATA-accredited
laboratory at the supplier's expense.
For documentation, the supplier must establish
a compliance folder that includes a signed
DoC, test reports, and a technical description
of the product.
Compliance Level 3. Level 3 requirements
encompass high-risk devices likely to
generate emissions with a high potential
to cause interference with communications.
This compliance level currently applies
to only two categories of equipment: Group
2 ISM devices under AS/NZS 2064 (CISPR
11) and telecommunication products requiring
A-tick under AS/NZS 3548 (CISPR 22). Because
it requires the highest confidence of
compliance, a NATA or NATA MRA-partner
conformance report is mandatory. The supplier
must establish a compliance folder that
includes a signed DoC, a technical description
of the product, and an accredited test
report.
Documentary Recordkeeping. The
EMC regulation lays down minimum requirements
for the content of a compliance folder.
The supplier must retain the compliance
folder and all relevant records for a
period of five years after the date of
last sale of the device. The compliance
folder may be stored electronically, but
it must be produced for ACA audit or investigation
purposes within 10 working days of a written
request. The DoC must be held in Australia
at the registered supplier code address.
Keeping the compliance folder overseas
is permissible, but the supplier should
check that it contains the necessary information
before committing it to storage.
Enforcement. The ACA is the enforcement
body, and regards it as an obligation to
responsible suppliers who comply with the
regulations to ensure that an effective
enforcement mechanism operates. This is
critical for a system based on self-declaration
by suppliers. The general policy of the
ACA is to enforce the regulations by educating
suppliers and by negotiating in order to
resolve problems and complaints. As a last
resort, the ACA will use the penalty provisions
against suppliers who are in willful violation
of the regulations.
If a product's compliance is questioned,
the ACA will conduct an audit of the compliance
folder and may undertake further investigations.
Penalties for willful violations can be
imposed on both individuals and companies,
with regulations enforceable under the
Radiocommunications Act 1992, the Trade
Practices Act 1974, the Telecommunications
Act 1997, and the Crimes Act 1914. Prosecution
for breaches of the C-tick labeling provisions
under trademark and copyright regulations
is also possible.
The supply of a nonstandard device, a
primary offense under the Radiocommunications
Act, may result in the seizure and forfeiture
of stock and up to $160,000 in criminal
penalties. Imprisonment is a possible
punishment under the Crimes Act.
The ACA can issue a notice to prohibit
the sale or use of a device that is causing
interference until the problem is corrected.
Provisions exist for fines of up to $12,000
per day for the period of the infringement.
A system of on-the-spot fines for minor
transgressions is also in place. In addition,
failure to prepare and maintain a compliance
folder that adheres to the ACA requirements
for a device imported or placed on the
market may constitute a number of offenses.
If the ACA auditor is not satisfied
with the evidence of compliance, then an
accredited report demonstrating compliance
must be provided within 30 working days
of request. The supplier may also be required
to submit three samples of the device to
a NATA-accredited test laboratory nominated
by the ACA. All testing costs must be borne
by the supplier.
The Testing Route. The most
common and cost-effective means of compliance
with the EMC framework involves testing
against the ACA emission standards. EMC
test houses are accredited by NATA to
specific EMC standards in accordance with
IEC Guide 25. The test report to be included
in the compliance folder must be in English,
and, if not an original, must be a certified
copy. Product variants whose altered features
are irrelevant to the question of RF emissions
or do not increase RF emissions can be
presumed to comply. The supplier may market
any number of such product variants under
a single DoC. However, the compliance
folder must identify variants and contain
descriptions of the changes made to the
basic model. It must also include the
rationale for marketing the device and
its variants under the one DoC.
The Technical Construction File Route.
In some cases, a technical construction
file (TCF) can be prepared and submitted
to a competent body for assessment. The
TCF route is intended to be used when
the product is too large or otherwise
impossible to test or when there are a
large number of variants of a basic model.
The Australian EMC regulation permits
either the testing or the TCF route to
compliance to be taken at the discretion
of the supplier. The Australian TCF route
is virtually identical to the European
TCF route. The only difference is that
compliance is assessed against specific
emission standards (limits) in Australia;
whereas, in the European Union compliance
is assessed against broadly based noninterference
requirements.
The Role of the Competent Body.
Competent bodies (CBs) are accredited
by NATA in accordance with the requirements
of IEC Guide 39/EN 45004, Guidelines for
the Accreditation of Inspection Bodies.
The role of the CB is to provide a technical
report based on technical assessment of
the TCF prepared and submitted by the
supplier and which confirms the claims
of compliance made by the supplier. Any
testing requested by the CB must be NATA
accredited. The report issued by a CB
will be a NATA-endorsed document that
will have the same status as a NATA test
report. Only NATA-accredited CBs are able
to issue endorsed reports against TCFs.
A competent body may not approve
test reports, whether accredited or not,
and it may not conduct testing itself as
part of the assessment of a TCF unless it
has NATA accreditation for that testing
and unless the testing and CB functions
are totally independent of each other. Only
organizations like NATA can approve test
laboratories or manufacturers' in-house
testing.
When the CB requires extra testing in
support of a TCF assessment, it may use
only NATA-accredited testing or its equivalent.
These test data may be used in conjunction
with other data supplied by the manufacturer,
including nonaccredited testing, in the
assessment of the device against the appropriate
standard. The TCF route to compliance
is generally not cost-effective except
when there are a number of variations
of the same model within a family of products.
Some very large or complex products can
be difficult or impractical to transport
to a test laboratory. For these, the supplier
may prepare a TCF with assistance from
a CB. The TCF route to compliance may
be the best for large and complex products.
In these cases, some standards permit
in situ testing at the user installation;
this option should be seriously considered,
especially for single installations. As
more EMC standards permit in situ tests
for products that are difficult to test
at a test house, the supplier is advised
to consult with a test laboratory accredited
by NATA for testing to the standard in
question or to seek advice from a competent
body.
Product variants are approached in a
manner similar to that of the TCF route
under the EMC Directive. In cases involving
product variations, the supplier must
identify variants that are benign and
those that do not require testing or CB
assessment of a TCF. The ACA framework
specifically allows the presumption of
compliance for electromagnetically benign
products and those variants of a basic
model that are irrelevant to the RF characteristics
of the device (cosmetic changes) or that
do not increase the RF emission characteristics
established for the basic model. The supplier
can legally claim compliance under these
circumstances without testing and without
the involvement of a CB. It is still necessary
to prepare a compliance folder for that
product.
An MRA between the European Union
and Australia/New Zealand was ratified in
1999. This MRA facilitates the acceptance
of testing and CB reports among Australia,
New Zealand, and the EU member countries.
The EU CBs must be accredited to the ACA
requirements, and the Australian CBs must
be accredited to the EU EMC Directive.
Compliance with the Australian EMC regulations
became mandatory on January 1, 1999. All
products encompassed by the scope of the
mandated standards and marketed in Australia
must be labeled with a C-tick and supported
by a compliance folder maintained at the
disposal of the ACA. The ACA actively
enforces the self-certification system
by the regular audit of compliance folders.
Following extensive industry consultation,
the new Australian EMC regulations are now
firmly entrenched. The C-tick scheme is
widely regarded as a success. General industry
and community awareness of the C-tick is
very high, and the ACA strategy of conciliation
and education has fostered industry cooperation.
Despite a certain spirited opposition and
difficulties experienced by some industry
sectors, implementation of the new EMC regulations
has gone well.
Chris Zombolas is technical director
at EMC Technologies Pty Ltd. (Melbourne,
Victoria, Australia).
Illustration by Bob
Schuchman