Therapeutic Goods (Charges) Act 1989

3 Incorporation

(1) The Therapeutic Goods Act 1989 is incorporated, and is to be read as one, with this Act.

Note: Subsection (1) applies the interpretation provisions of the Therapeutic Goods Act 1989 (such as subsection 3(8) of that Act, which says a reference to the registration of therapeutic goods includes a reference to the provisional registration of a medicine).

(1A) For the purposes of this Act, if a suspension of the registration or listing of therapeutic goods has effect under Therapeutic Goods Act 1989, the goods are taken to be included in the Register under that Part.Part 3-2 of the

(1B) For the purposes of this Act, if a suspension of a biological from the Register has effect under Therapeutic Goods Act 1989, the biological is taken to be included in the Register under that Part.Part 3-2A of the

(2) For the purposes of this Act, if a suspension of a kind of medical device, or any medical devices of a particular kind, has effect under Chapter 4 of the Therapeutic Goods Act 1989, that kind of medical device is taken to be included in the Register under that Chapter.

(3) For the purposes of this Act, if a suspension of a conformity assessment body determination has effect under regulations made for the purposes of Therapeutic Goods Act 1989, the determination is taken to be in force for the period of the suspension.Part 4-4A of the

4 Charges

Annual charges of such amounts as are prescribed are payable in respect of the registration or listing of therapeutic goods, other than grouped therapeutic goods, that is in force at any time during a financial year.

Note: The reference to registration of therapeutic goods includes a reference to the provisional registration of a medicine (see subsection 3(8) of the Therapeutic Goods Act 1989 as applied by subsection 3(1) of this Act).

If the registration or listing of one or more grouped therapeutic goods, being goods covered by a single registration or listing number, is in force at any time during a financial year, an annual charge of such amount as is prescribed is payable in respect of all of the registrations or listings concerned.

(1AA) An annual charge of such amount as is prescribed is payable in respect of the inclusion of a biological in the Register under Part 3-2A of the Therapeutic Goods Act that has effect at any time during a financial year.

Annual charges of such amounts as are prescribed are payable in respect of the inclusion of kinds of medical devices in the Register under Chapter 4 of the Therapeutic Goods Act that has effect at any time during a financial year.

An annual charge of such amount as is prescribed is payable in respect of a licence that is in force at any time during a financial year.

An annual charge of such amount as is prescribed is payable in respect of a conformity assessment body determination that is in force at any time during a financial year.

Corresponding State laws

If, because of the operation of section 6AAE of the Therapeutic Goods Act, goods are included in the part of the Register for goods known as registered goods, this section has effect as if the goods had been registered under Part 3-2 of that Act.

If, because of the operation of section 6AAE of the Therapeutic Goods Act, goods are included in the part of the Register for goods known as provisionally registered goods, this section has effect as if the goods had been registered under Part 3-2 of that Act.

If, because of the operation of section 6AAE of the Therapeutic Goods Act, goods are included in the part of the Register for goods known as listed goods, this section has effect as if the goods had been listed under Part 3-2 of that Act.

If, because of the operation of section 6AAE of the Therapeutic Goods Act, a biological is included in the part of the Register for biologicals included under Part 3-2A, this section has effect as if the biological had been included in the Register under Part 3-2A of that Act.

If, because of the operation of section 6AAE of the Therapeutic Goods Act, goods are included in the part of the Register for medical devices included under Chapter 4, this section has effect as if the goods had been included in the Register under Chapter 4 of that Act.

If:

because of the operation of the Secretary issues a licence; andsection 6AAA, 6AAB or 6AAC of the Therapeutic Goods Act,

the licence is issued for the purposes of provisions of a corresponding State law that correspond to Part 3-3 of the Therapeutic Goods Act;

this section has effect as if the licence had been issued under Part 3-3 of that Act.

Definitions

In this section:

amount includes a nil amount.

Therapeutic Goods Act means the Therapeutic Goods Act 1989.

5 Regulations

The Governor-General may make regulations, not inconsistent with this Act, prescribing the amounts of charges.

The regulations may prescribe different charges in relation to:

different classes of goods (including medical devices); or

in the case of annual licensing charges—different steps in the manufacture of goods; or

conformity assessment body determinations of different kinds.

Endnotes

Endnote 1—About the endnotes

The endnotes provide information about this compilation and the compiled law.

The following endnotes are included in every compilation:

Endnote 1—About the endnotes

Endnote 2—Abbreviation key

Endnote 3—Legislation history

Endnote 4—Amendment history

Abbreviation key—Endnote 2

The abbreviation key sets out abbreviations that may be used in the endnotes.

Legislation history and amendment history—Endnotes 3 and 4

Amending laws are annotated in the legislation history and amendment history.

The legislation history in endnote 3 provides information about each law that has amended (or will amend) the compiled law. The information includes commencement details for amending laws and details of any application, saving or transitional provisions that are not included in this compilation.

The amendment history in endnote 4 provides information about amendments at the provision (generally section or equivalent) level. It also includes information about any provision of the compiled law that has been repealed in accordance with a provision of the law.

Editorial changes

The Legislation Act 2003 authorises First Parliamentary Counsel to make editorial and presentational changes to a compiled law in preparing a compilation of the law for registration. The changes must not change the effect of the law. Editorial changes take effect from the compilation registration date.

If the compilation includes editorial changes, the endnotes include a brief outline of the changes in general terms. Full details of any changes can be obtained from the Office of Parliamentary Counsel.

Misdescribed amendments

A misdescribed amendment is an amendment that does not accurately describe the amendment to be made. If, despite the misdescription, the amendment can be given effect as intended, the amendment is incorporated into the compiled law and the abbreviation “(md)” added to the details of the amendment included in the amendment history.

If a misdescribed amendment cannot be given effect as intended, the abbreviation “(md not incorp)” is added to the details of the amendment included in the amendment history.

Endnote 2—Abbreviation key

Endnote 3—Legislation history

Endnote 4—Amendment history

Endnote 5—Editorial changes

In preparing this compilation for registration, the following kinds of editorial change(s) were made under the Legislation Act 2003.

Long t itle

Kind of editorial change

Change to punctuation

Details of editorial change

Schedule 1 item 1 of the Therapeutic Goods (Charges) Amendment Act 2018 provides as follows:

1 Title

Omit “and on the licensing of manufacturers of therapeutic goods”, substitute “, on the licensing of manufacturers of therapeutic goods and on the making of conformity assessment body determinations”.

This action leaves two commas before the phrase “on the licensing”.

This compilation was editorially changed to omit the redundant comma.