The Patents Act 1990 is Australia’s main law creating a quid‑pro‑quo: inventors disclose how inventions work in exchange for temporary exclusive rights (standard patents ~20 years; innovation patents ~8 years, noting new innovation patents are no longer granted). It sets rules on what is patentable, how to apply and examine applications, ownership/transfer, and how patents can be challenged or extended (notably for delayed drug approvals).
It affects inventors, businesses, competitors, consumers and pharma firms — balancing incentives to innovate with eventual public access and influencing medicine prices and technology diffusion.
The Patents Act 1990 (Cth) establishes a dual‑track patent system in Australia that rewards inventiveness while balancing the interests of rights holders, technology users and the public. Its object, expressed in section 2A, is to promote economic wellbeing through technological innovation and the transfer and dissemination of technology. The Act creates two species of patent:
standard patents (ss 18(1), 67) with a 20‑year term, requiring an inventive step; and
innovation patents (ss 18(1A), 68) with an 8‑year term, requiring only an innovative step, although the innovation patent system has been closed to new filings (ss 52(3), 101B(2)(ha)).
A patent gives the patentee the exclusive right, during the patent term, to exploit the invention and to authorise others to do so (s 13). The Act then provides a comprehensive lifecycle: application and examination, acceptance, grant, maintenance, amendment, exploitation, Crown use, compulsory licensing, infringement remedies, revocation and the professional regulation of patent attorneys. It also contains specific regimes for pharmaceutical patent term extensions, divisional applications, patents of addition, associated technology under the Safeguards Act, and the implementation of the Patent Cooperation Treaty (PCT) and the Budapest Treaty.
Main concepts
Current sections
Direct links to the current provisions in Patents Act 1990.
290
1
Short title
1 Short title
This Act may be cited as the Patents Act 1990.
2
Commencement
2 Commencement
(1) Subject to subsection (2), this Act commences on a day to be fixed by Proclamation.
(2) If this Act does not commence under subsection (1) within the period of 6 months beginning on the day on which it receives the Royal Assent, it commences on the first day after the end of that period.
2A
Object of this Act
2A Object of this Act
The object of this Act is to provide a patent system in Australia that promotes economic wellbeing through technological innovation and the transfer and dissemination of technology. In doing so, the patent system balances over time the interests of producers, owners and users of technology and the public.
3
Definitions
3 Definitions
The following expressions are defined, for the purposes of this Act or of a particular Chapter of this Act, in the dictionary in Schedule 1:
5
Associated applications
5 Associated applications
For the purposes of this Act, a complete application is to be taken to be associated with a provisional application if, and only if, the patent request filed in respect of the complete application identifies the provisional application and contains a statement to the effect that the applications are associated.
[Note: see sections 29 and 38]
6
Deposit requirements
6 Deposit requirements
For the purposes of this Act, the deposit requirements are to be taken to be satisfied in relation to a micro‑organism to which a specification relates if, and only if:
(a) the micro‑organism was, on or before the date of filing of the specification, deposited with a prescribed depositary institution in accordance with the rules relating to micro‑organisms; and
(b) the specification includes, at that date, such relevant information on the characteristics of the micro‑organism as is known to the applicant; and
(c) at all times since the end of the prescribed period, the specification has included:
(i) the name of a prescribed depositary institution from which samples of the micro‑organism are obtainable as provided by the rules relating to micro‑organisms; and
(iii) the file, accession or registration number of the deposit given by the institution; and
(d) at all times since the date of filing of the specification, samples of the micro‑organism have been obtainable from a prescribed depositary institution as provided by those rules.
[Note: see sections 41 and 42]
7
Novelty, inventive step and innovative step
7 Novelty, inventive step and innovative step
Novelty
(1) For the purposes of this Act, an invention is to be taken to be novel when compared with the prior art base unless it is not novel in the light of any one of the following kinds of information, each of which must be considered separately:
(a) prior art information (other than that mentioned in paragraph (c)) made publicly available in a single document or through doing a single act;
(b) prior art information (other than that mentioned in paragraph (c)) made publicly available in 2 or more related documents, or through doing 2 or more related acts, if the relationship between the documents or acts is such that a person skilled in the relevant art would treat them as a single source of that information;
(c) prior art information contained in a single specification of the kind mentioned in subparagraph (b)(ii) of the definition of prior art base in Schedule 1.
Inventive step
(2) For the purposes of this Act, an invention is to be taken to involve an inventive step when compared with the prior art base unless the invention would have been obvious to a person skilled in the relevant art in the light of the common general knowledge as it existed (whether in or out of the patent area) before the priority date of the relevant claim, whether that knowledge is considered separately or together with the information mentioned in subsection (3).
(3) The information for the purposes of subsection (2) is:
(a) any single piece of prior art information; or
(b) a combination of any 2 or more pieces of prior art information that the skilled person mentioned in subsection (2) could, before the priority date of the relevant claim, be reasonably expected to have combined.
Innovative step
(4) For the purposes of this Act, an invention is to be taken to involve an innovative step when compared with the prior art base unless the invention would, to a person skilled in the relevant art, in the light of the common general knowledge as it existed (whether in or out of the patent area) before the priority date of the relevant claim, only vary from the kinds of information set out in subsection (5) in ways that make no substantial contribution to the working of the invention.
(5) For the purposes of subsection (4), the information is of the following kinds:
(a) prior art information made publicly available in a single document or through doing a single act;
(b) prior art information made publicly available in 2 or more related documents, or through doing 2 or more related acts, if the relationship between the documents or acts is such that a person skilled in the relevant art would treat them as a single source of that information.
(6) For the purposes of subsection (4), each kind of information set out in subsection (5) must be considered separately.
[Notes: (1) For the meaning of document see section 2B of the Acts Interpretation Act 1901.
(2) See also the definitions of prior art base and prior art information in Schedule 1: see also paragraph 18(1)(b) and section 98.]
7A
Meaning of useful
7A Meaning of useful
(1) For the purposes of this Act, an invention is taken not to be useful unless a specific, substantial and credible use for the invention (so far as claimed) is disclosed in the complete specification.
(2) The disclosure in the complete specification must be sufficient for that specific, substantial and credible use to be appreciated by a person skilled in the relevant art.
(3) Subsection (1) does not otherwise affect the meaning of the word useful in this Act.
9
Secret use
9 Secret use
For the purposes of this Act, the following acts are not to be taken to be secret use of an invention in the patent area:
(a) any use of the invention by or on behalf of, or with the authority of, the patentee or nominated person, or his or her predecessor in title to the invention, for the purpose of reasonable trial or experiment only;
(b) any use of the invention by or on behalf of, or with the authority of, the patentee or nominated person, or his or her predecessor in title to the invention, being use occurring solely in the course of a confidential disclosure of the invention by or on behalf of, or with the authority of, the patentee, nominated person, or predecessor in title;
(c) any other use of the invention by or on behalf of, or with the authority of, the patentee or nominated person, or his or her predecessor in title to the invention, for any purpose other than the purpose of trade or commerce;
(d) any use of the invention by or on behalf of the Commonwealth, a State, or a Territory where the patentee or nominated person, or his or her predecessor in title to the invention, has disclosed the invention, so far as claimed, to the Commonwealth, State or Territory;
(e) any use of the invention by or on behalf of, or with the authority of, the patentee or nominated person, or his or her predecessor in title to the invention, for any purpose, if a complete application is made for the invention within the prescribed period.
[Note: See also paragraph 18(1)(d)]
10
Certain international applications to be taken to have been given an international filing date
10 Certain international applications to be taken to have been given an international filing date
(1) Where:
(a) an international application specifies Australia as a designated State under Article 4(1)(ii) of the PCT; and
(b) the receiving Office does not give the application an international filing date; and
(c) the Commissioner is satisfied, on the balance of probabilities, that the application should, under Article 25(2)(a) of the PCT, be treated as if it had been given an international filing date;
the application is to be taken, for the purposes of this Act, to have been given an international filing date under Article 11 of the PCT.
(2) This section does not apply to an international application that was not filed in the receiving Office in English unless the following documents have been filed:
(a) a translation of the application into English;
(b) if required by the regulations—a certificate of verification (within the meaning of the regulations) of the translation.
(3) Where this section applies, the international filing date of the application is to be taken to be the date that, in the opinion of the Commissioner, should have been given to the application as its international filing date under the PCT.
[Note: international filing date is defined in Schedule 1.]
11
Act binds the Crown
11 Act binds the Crown
(1) This Act binds the Crown in right of the Commonwealth, of each of the States, of the Australian Capital Territory and of the Northern Territory.
(2) Nothing in this Act makes the Crown liable to be prosecuted for an offence.
12
Application of Act
12 Application of Act
This Act extends to:
(a) each external Territory; and
(b) the Australian continental shelf; and
(c) the waters above the Australian continental shelf; and
(d) the airspace above Australia, each external Territory and the Australian continental shelf.
12A
Application of the Criminal Code
12A Application of the Criminal Code
Chapter 2 of the Criminal Code applies to all offences created by this Act.
Note: Chapter 2 of the Criminal Code sets out the general principles of criminal responsibility.
Chapter 2—Patent rights, ownership and validity
Part 1
Patent rights
Part 1—Patent rights
13
Exclusive rights given by patent
13 Exclusive rights given by patent
(1) Subject to this Act, a patent gives the patentee the exclusive rights, during the term of the patent, to exploit the invention and to authorise another person to exploit the invention.
(2) The exclusive rights are personal property and are capable of assignment and of devolution by law.
(3) A patent has effect throughout the patent area.
14
Assignment of patent
14 Assignment of patent
(1) An assignment of a patent must be in writing signed by or on behalf of the assignor and assignee.
(2) A patent may be assigned for a place in, or part of, the patent area.
Part 2
Ownership
Part 2—Ownership
15
Who may be granted a patent?
15 Who may be granted a patent?
(1) Subject to this Act, a patent for an invention may only be granted to a person who:
(a) is the inventor; or
(b) would, on the grant of a patent for the invention, be entitled to have the patent assigned to the person; or
(c) derives title to the invention from the inventor or a person mentioned in paragraph (b); or
(d) is the legal representative of a deceased person mentioned in paragraph (a), (b) or (c).
(2) A patent may be granted to a person whether or not he or she is an Australian citizen.
16
Co‑ownership of patents
16 Co‑ownership of patents
(1) Subject to any agreement to the contrary, where there are 2 or more patentees:
(a) each of them is entitled to an equal undivided share in the patent; and
(b) each of them is entitled to exercise the exclusive rights given by the patent for his or her own benefit without accounting to the others; and
(c) none of them can grant a licence under the patent, or assign an interest in it, without the consent of the others.
(2) Where a patented product, or a product of a patented method or process, is sold by any of 2 or more patentees, the buyer, and a person claiming through the buyer, may deal with the product as if it had been sold by all the patentees.
(3) This section does not affect the rights or obligations of a trustee or of the legal representative of a deceased person, or rights or obligations arising out of either of those relationships.
17
Directions to co‑owners
17 Directions to co‑owners
(1) Where there are 2 or more patentees, the Commissioner may, on the application of any of them, give such directions in accordance with the application as the Commissioner thinks fit, being directions about:
(a) a dealing with the patent or an interest in it; or
(b) the grant of licences under the patent; or
(c) the exercise of a right under section 16 in relation to the patent.
(2) If a patentee fails to do anything necessary to carry out a direction under subsection (1) within 14 days after being asked in writing to do so by one of the other patentees, the Commissioner may, on the application of one of those other patentees, direct a person to do it in the name and on behalf of the defaulting patentee.
(3) Before giving a direction, the Commissioner must give an opportunity to be heard:
(a) in the case of an application by a patentee or patentees under subsection (1)—to the other patentee or patentees; and
(b) in the case of an application under subsection (2)—to the defaulting patentee.
(4) The Commissioner must not give a direction that:
(a) affects the rights or obligations of a trustee or of the legal representative of a deceased person, or rights or obligations arising out of either of those relationships; or
(b) is inconsistent with the terms of an agreement between the patentees.
More sections below
Source text: opening excerpt
Sourced from the Federal Register of Legislation (legislation.gov.au), CC BY 4.0.
1 Short title
1 Short title
This Act may be cited as the Patents Act 1990.
2 Commencement
2 Commencement
(1) Subject to subsection (2), this Act commences on a day to be fixed by Proclamation.
(2) If this Act does not commence under subsection (1) within the period of 6 months beginning on the day on which it receives the Royal Assent, it commences on the first day after the end of that period.
2A Object of this Act
2A Object of this Act
The object of this Act is to provide a patent system in Australia that promotes economic wellbeing through technological innovation and the transfer and dissemination of technology. In doing so, the patent system balances over time the interests of producers, owners and users of technology and the public.
3 Definitions
3 Definitions
The following expressions are defined, for the purposes of this Act or of a particular Chapter of this Act, in the dictionary in Schedule 1:
5 Associated applications
5 Associated applications
For the purposes of this Act, a complete application is to be taken to be associated with a provisional application if, and only if, the patent request filed in respect of the complete application identifies the provisional application and contains a statement to the effect that the applications are associated.
[Note: see sections 29 and 38]
6 Deposit requirements
6 Deposit requirements
For the purposes of this Act, the deposit requirements are to be taken to be satisfied in relation to a micro‑organism to which a specification relates if, and only if:
(a) the micro‑organism was, on or before the date of filing of the specification, deposited with a prescribed depositary institution in accordance with the rules relating to micro‑organisms; and
(b) the specification includes, at that date, such relevant information on the characteristics of the micro‑organism as is known to the applicant; and
(c) at all times since the end of the prescribed period, the specification has included:
(i) the name of a prescribed depositary institution from which samples of the micro‑organism are obtainable as provided by the rules relating to micro‑organisms; and
(iii) the file, accession or registration number of the deposit given by the institution; and
(d) at all times since the date of filing of the specification, samples of the micro‑organism have been obtainable from a prescribed depositary institution as provided by those rules.
The architecture of the Act is built around the patentability criteria in section 18, interpreted through definitions in Schedule 1 and elaborated in sections 7, 7A and 9.
Patentable invention. For a standard patent, each claim must be a “manner of manufacture”, novel, involve an inventive step, be useful and not have been secretly used (s 18(1)). For an innovation patent the criteria are the same except “innovative step” replaces “inventive step” (s 18(1A)). Certain subject matter is excluded: human beings and biological processes for their generation cannot be patented at all (s 18(2)); for innovation patents, plants, animals and biological processes for their generation are also excluded unless the invention is a microbiological process or product (s 18(3)-(4)).
Novelty, inventive step and innovative step. The prior art base is defined in Schedule 1.
Novelty (s 7(1)): an invention is novel unless, against the prior art base, it is not new when compared with (a) a single document or act, (b) two or more related documents or acts that a skilled person would treat as a single source, or (c) a single prior‑filed specification of a particular kind. Each piece of information is considered separately.
Inventive step (s 7(2)-(3)): an invention lacks an inventive step if it would have been obvious to a person skilled in the art in light of common general knowledge (anywhere) before the priority date, considered alone or together with a single piece of prior art, or with a combination of pieces that the skilled person could reasonably have been expected to combine.
Innovative step (s 7(4)-(6)): an invention lacks an innovative step if, to a skilled person, it would only vary from prior art (single documents/acts or related sources treated as a single source, considered separately) in ways that make no substantial contribution to the working of the invention.
Useful (s 7A): an invention is not useful unless the complete specification discloses a specific, substantial and credible use sufficiently clear for a skilled person to appreciate it. This does not otherwise alter the meaning of “useful” (s 7A(3)).
Secret use. Section 9 deems certain acts not to be secret use: reasonable trial or experiment, confidential disclosures, use for non‑trade purposes, use by the Crown after disclosure and use made public before the patent application’s priority date, among others.
Specifications. A provisional specification must disclose the invention sufficiently (s 40(1)). A complete specification must describe it fully, disclose the best method and end with claims that are clear, succinct and supported by the matter disclosed (s 40(2)-(3)). Claims must not rely on references to descriptions or drawings unless absolutely necessary (s 40(3A)). Innovation patents are limited to five claims (s 40(2)(c)). Where an invention involves a micro‑organism, the deposit requirements in section 6 must be met for the specification to be adequate (s 41). If a deposited organism ceases to be reasonably available, the Commissioner or a court may declare the specification non‑compliant (s 42).
Priority date. Each claim has a priority date, generally the filing date of the specification first disclosing it, but regulations may provide for an earlier date based on an earlier related application (s 43). A subsequent Convention application can displace an earlier withdrawn application for priority purposes (s 43(5)).
Examination, acceptance and grant. A standard patent application proceeds through examination (ss 44-45), acceptance (s 49) and grant (s 61). The Commissioner must accept if, on the balance of probabilities, the specification meets section 40(2)-(4) and the invention satisfies the criteria in section 18(1)(a)-(c) (s 49(1)). Acceptance may be postponed (s 49A) or revoked before grant (s 50A). Innovation patents undergo a formalities check (s 52) and are granted on acceptance (s 62). They cannot be enforced unless examined and certified (s 120(1A)); examination leads to certification or revocation (ss 101A-101F). Both types of patent may be re‑examined after grant (standard: Ch 9, innovation: Ch 9A Pt 2) and are subject to opposition (standard: Ch 5, innovation: Ch 9A Pt 3).
Infringement and remedies. Infringement is addressed in Chapter 11. The patentee or exclusive licensee may sue for infringement (s 120). Relief includes an injunction and, at the plaintiff’s option, damages (including additional damages for flagrancy) or an account of profits (s 122). Innocent infringers may escape monetary relief but not an injunction (s 123). Specific exemptions cover temporary foreign vessels, aircraft and land vehicles (s 118), prior use (s 119), acts done solely for regulatory approval of pharmaceuticals (s 119A) or non‑pharmaceuticals (s 119B), and experimental use relating to the subject matter of the invention (s 119C). A separate cause of action exists for unjustified threats of infringement proceedings (ss 128-132).
Crown exploitation, compulsory licensing and prohibition orders. The Crown may exploit a patented invention for the services of a relevant authority under either a general pathway (s 163) or an emergency pathway (s 163A), subject to remuneration (s 165). Compulsory licences may be granted by the Federal Court (s 133), with a dedicated Part for patented pharmaceutical inventions for export to eligible importing countries (Ch 12 Pt 3). The Commissioner may make prohibition orders restricting publication in the interests of defence (s 173) or for associated technology (ss 152-153).
Patent attorneys. Chapter 20 establishes a registration and discipline regime. Registered patent attorneys enjoy a statutory privilege for communications made for the dominant purpose of providing intellectual property advice, equivalent to legal professional privilege (s 200(2)-(2C)). The Designated Manager keeps the Register of Patent Attorneys (s 198). The Trans‑Tasman IP Attorneys Board oversees qualifications, deregistration and professional conduct (s 227A).
Who it affects
The Act touches a wide population.
Applicants, nominated persons and patentees: individuals, companies, universities and research institutions that seek or hold patent rights.
Exclusive licensees: may sue for infringement and must be party to certain proceedings (s 120(2), s 139(1)).
The Commissioner of Patents and Deputy Commissioners: charged with examination, acceptance, grant, re‑examination, extensions of time, coercive evidence‑gathering and many discretionary decisions.
The Designated Manager: responsible for the patent attorneys register and for intervening when an incorporated patent attorney lacks a patent attorney director (ss 198, 200A, 201B).
The Trans‑Tasman IP Attorneys Board: sets professional standards and disciplinary rules for patent attorneys (s 227A).
The Crown: the Commonwealth, States and Territories, and relevant authorities have statutory exploitation and acquisition rights (Ch 17).
Third parties: persons opposing grants (s 59) or extensions (s 75), seeking revocation (s 138), applying for non‑infringement declarations (s 125), requesting examination of an innovation patent (s 101A(1)(b)), making unjustified threats claims (s 128), or applying for compulsory licences (s 133).
Patent attorneys (individuals and incorporated entities) and legal practitioners: subject to the conduct and offence provisions of Chapter 20.
Generic pharmaceutical manufacturers: may rely on the regulatory approval exemption (s 119A) or apply for compulsory PPI licences.
The public: may inspect the Register (s 190) and certain documents (s 193).
Key duties and rights
Patentee and exclusive licensee rights. A patentee has the exclusive right to exploit the invention (s 13). Infringement proceedings may be brought in a prescribed court or the Federal Court; for innovation patents, the patent must be certified first (s 120(1A)). An exclusive licensee may sue, with the patentee joined as a defendant unless joined as plaintiff (s 120(2)). The limitation period is the later of three years from grant or six years from the infringing act (s 120(4)).
Crown rights and duties. A relevant authority may exploit a patented invention for Crown purposes without infringing, provided the relevant Minister gives a written approval and, for the general pathway, the authority has tried for a reasonable period to obtain the patentee’s authorisation on reasonable terms, and at least 14 days’ written notice of the approval is given before exploitation starts (s 163(3)). In an emergency, approval must be obtained before exploitation starts and notice given as soon as practicable afterwards (s 163A). The Crown must pay remuneration on terms agreed or determined by a court (s 165). Once terms exist, failure to comply constitutes infringement (ss 163(2), 163A(2)).
Applicant and patentee duties. An applicant for a standard patent must request examination within the prescribed period (s 44); failure to do so causes the application to lapse (s 142(2)(a)). Applicants and patentees must pay continuation or renewal fees (ss 142(2)(d), 143, 143A). They may amend the specification, but amendments must not extend beyond the as‑filed disclosure or, after acceptance or certification, widen the claims or breach section 40(2)-(3A) (s 102). Amendments require consent of a mortgagee or exclusive licensee (s 103).
Commissioner’s duties and powers. The Commissioner must examine applications (s 45), accept or refuse them (ss 49-50), grant patents (s 61), maintain the Register (s 186), rectify it on specified grounds (s 191A), award costs (s 210(1)(d)) and extend time in three tiers:
mandatory extension if the failure was caused by an error or omission of the Patent Office, a service provider, the receiving Office or the International Bureau (s 223(1));
discretionary extension for errors or omissions by the person or their agent, or circumstances beyond control (s 223(2)); and
a “due care” extension, which the Commissioner must grant if satisfied the person took due care to do the act in time, limited to a prescribed maximum period (s 223(2A)-(2B)).
The Commissioner may, for the purposes of the Act, summon witnesses, receive evidence on oath, require production of documents and award costs (s 210(1)). Before exercising a power adversely, the Commissioner must give the person a reasonable opportunity to be heard (s 216(1)), except for directing a request for examination (s 216(2)).
Patent attorney privilege. Communications and records made for the dominant purpose of a registered patent attorney providing “intellectual property advice” are privileged to the same extent as legal professional privilege (s 200(2)-(2C)). The privilege extends to foreign individuals authorised to provide such advice, but “intellectual property advice” does not cover advice of a purely scientific or technical nature (s 200(2C)).
Duties of incorporated patent attorneys. An incorporated patent attorney must have at least one patent attorney director. If it ceases to have one, it must notify the Designated Manager within seven days and must not carry on business after that period without a director (s 201B(1)-(2)). The Designated Manager may appoint a replacement attorney (with consent) to take charge of its patents work or remove the entity from the Register (s 201B(3)-(7)).
Public access. After acceptance of a standard patent application, the specification becomes open to public inspection (OPI) (s 55). The Register of Patents is open for public inspection (s 190). From the time a complete specification becomes OPI until grant, the applicant has the same rights as if a patent had been granted, but cannot start proceedings until grant (s 57).
Penalties and enforcement
The Act deploys a mixture of civil remedies, criminal offences and administrative sanctions.
Civil remedies. Infringement attracts an injunction and, at the plaintiff’s option, damages or an account of profits (s 122(1)). Additional damages may be awarded for flagrant infringement, the need for deterrence, the infringer’s post‑infringement conduct, the benefit to the infringer and any other relevant matter (s 122(1A)). A court may refuse damages or an account if the defendant proves innocent infringement (unawareness and no reason to believe a patent existed); knowledge is presumed if patented products were marked and substantially sold or used in the patent area (s 123). A person aggrieved by unjustified threats of proceedings may obtain a declaration, an injunction and damages (including additional damages) (s 128).
Criminal offences. The following attract specified penalties:
false representation of connection with the Patent Office: 30 penalty units (s 177);
false representation that a person is a patentee or that an article is patented or the subject of an application: 60 penalty units; prosecution requires Ministerial consent (s 178);
officers trafficking in inventions or patents: 60 penalty units (s 182);
unauthorised disclosure of information by employees or others: imprisonment for two years (ss 183, 184);
false entries in the Register: imprisonment for two years (s 191);
patent attorney offences: acting or holding out without registration (s 201), failing to have a patent attorney director (s 201B), preparation of specifications by legal practitioners or unregistered persons outside supervised channels (ss 202, 202A, 202B), and failing to have an individual registered patent attorney in regular attendance and continuous charge at each office (s 203). Penalties range from 30 penalty units for individuals and partnerships to 150 penalty units for companies. For these attorney‑related offences, a prosecution may be started within five years of the offence (s 204), displacing the standard limitation period under the Crimes Act 1914.
contravention of prohibition orders (defence or associated technology): imprisonment for two years (ss 152(4), 173(2)).
Chapter 2 of the Criminal Code applies to all Act offences (s 12A).
Administrative sanctions. Where a person fails to comply with a summons or a requirement to produce documents under section 210, the Commissioner may, if satisfied on the balance of probabilities it is appropriate, refuse to grant a patent (if the person is an applicant), draw an adverse inference in proceedings or take prescribed actions (s 210A(2)). Before doing so, the Commissioner must consider any reasonable excuse, any offer of expenses and any other relevant matter (s 210A(3)). Costs awarded by the Commissioner are recoverable as a debt (s 211).
Revocation and cessation. A patent may be revoked by a prescribed court on grounds including lack of entitlement, non‑patentability, fraud or specification non‑compliance (s 138). An application lapses if the applicant does not meet deadlines (s 142); a standard patent ceases if renewal fees are not paid (s 143); an innovation patent ceases on similar grounds or if the Commissioner does not decide on certification within the prescribed period (s 143A).
Review and appeals. Specified decisions of the Commissioner, the Designated Manager and the Director (Safeguards) are reviewable by the Administrative Review Tribunal (ART) (s 224). These include decisions under ss 223 (extensions of time), 215 (death of patentee), 52 (innovation patent formalities), 137(3) (surrender), 141(1)(b) (withdrawal), 150(2) and 151(2) (restoration of lapsed applications) and a Designated Manager’s refusal to register a patent attorney (s 198). A decision substituted by the Commissioner under the computerised decision‑making power (s 223A) is also reviewable (s 224(1A)). Appeals against many Commissioner decisions lie to the Federal Court (e.g., s 51, s 60(4), s 104(7)); an appeal from a single judge’s decision on an appeal from the Commissioner to the Full Federal Court requires leave (s 158(2)).
How it interacts with other laws
The Patents Act 1990 does not operate in isolation.
Criminal Code: Chapter 2 applies to all offences under the Act (s 12A). Notes in Chapter 20 refer to evidential burdens under section 13.3(3) of the Code.
Corporations Act 2001: Related company groups for the patent attorney offence exceptions are determined under that Act (s 201(10)). An attorney appointed by the Designated Manager to take charge of an incorporated patent attorney’s work is not a director for the purposes of the Corporations Act (s 201B(6)).
Personal Property Securities Act 2009 (PPSA): The evidential status of the Register (s 195(3)) and the rule barring unregistered documents as proof of title (s 196(2)) do not apply to PPSA security interests.
Safeguards Act: Chapter 15 imports special provisions for associated technology, allowing the Director to issue certificates and directions that cause an application to lapse or to be withdrawn from international processing.
Trans‑Tasman mutual recognition: The Act recognises that it is immaterial whether events or decisions occur in New Zealand for purposes including patent attorney registration, deregistration and merits review (ss 198(12), 199(2), 227AB, 228(4C)-(4E)). The Trans‑Tasman IP Attorneys Board is continued under section 227A.
International treaties: Regulations may be made for giving effect to the PCT and the Budapest Treaty (s 228(1)(d)-(e)). A PCT application is treated as a complete application for a standard patent (s 29A). The TRIPS Agreement is also mentioned (s 228(1)(f)).
Therapeutic goods legislation: The regulatory approval exemption for pharmaceuticals in section 119A links to inclusion on the Australian Register of Therapeutic Goods; the definition of “pharmaceutical patent” in section 119A(3) is used to delimit the scope of the non‑pharmaceutical exemption in section 119B.
Administrative Review Tribunal Act 2024: Section 224 expressly references review by the ART and defines “decision” accordingly (s 224(4)). The Act also supplants the former AAT provisions.
1952 Act: Transitional provisions (Ch 23) preserve orders, directions, registers and patent attorney registrations made under the repealed legislation (ss 237, 239, 240).
Recent changes and why
The notes record several significant changes, all evident from the statutory text.
Innovation patent phase‑out. The formalities check for an innovation patent now requires that the date of the patent be before the day on which section 52(3) commenced (12 February 2021). Similarly, examination must confirm that the priority date of each claim is before the day section 101B(2)(ha) commenced (ss 101B(2)(ha), 101E(1)(viiia)). These amendments, introduced by the Intellectual Property Laws Amendment (Productivity Commission Response Part 2 and Other Measures) Act 2020, effectively close the innovation patent system to new filings.
Extensions of time for due care. The addition of sections 223(2A) and (2B) created a new “must grant” extension where the person took due care, but capped the period and required the application to be made after the time had expired (s 223(3A)).
Computerised decision‑making. Section 223A allows the Commissioner to use computer programs to make decisions and exercise powers. The Commissioner may substitute a decision if satisfied the computer‑generated decision is incorrect, and a substituted decision is subject to ART review (s 224(1A)).
Trans‑Tasman Board. Section 227A continued the former Professional Standards Board for Patent and Trade Marks Attorneys as the Trans‑Tasman IP Attorneys Board, with detailed membership and appointment provisions spanning Australia and New Zealand.
Migration to the ART. Section 224 was updated to refer to the Administrative Review Tribunal Act 2024, replacing the Administrative Appeals Tribunal pathway.
Court challenges and controversies
Although the notes do not reference decided cases, the text of the Act harbours several points that are inherently contentious and provide fertile ground for disputes.
Obviousness and the common general knowledge. The inventive step test in section 7(2)-(3) requires an assessment against common general knowledge “whether in or out of the patent area”. The availability of information artificially disaggregated or outside Australia, and the standard a court will apply to “could reasonably be expected to have combined”, is frequently debated.
Innovative step. The threshold of a “substantial contribution to the working of the invention” (s 7(4)-(6)) lacks legislative definition, and the requirement that variants be assessed against each prior art source “considered separately” makes the scope of the defence difficult to predict.
Prior use derivation exclusion. Section 119(3) strips the prior‑use defence if the product, method or process was derived from the patentee or predecessor, unless the derivation came from publicly available information disclosed in the grace period circumstances of section 24(1)(a). This demands a careful tracing of provenance and creates litigation risk for seemingly independent prior users.
Crown exploitation and remuneration. While the Crown enjoys statutory immunity during approved exploitation, the meaning of “reasonable terms” in section 163(3)(b) and the basis on which a court determines “just and reasonable” remuneration under section 165(2) (having regard to “the economic value of the exploitation” and any other relevant matter) are inherently value‑laden and apt to provoke disagreement.
Experimental use exemption. Section 119C exempts acts done “for experimental purposes relating to the subject matter of the invention”. The non‑exhaustive list in subsection (2) includes determining properties, improving or modifying, determining validity, and determining whether an act infringes. The boundary between permissible experimentation and commercial infringement remains a matter of ongoing practical tension.
Threats and mere notification. Section 131 declares that “mere notification of the existence of a patent is not a threat of infringement proceedings”. The line between a factual communication and an implied threat is fact‑sensitive and generates litigation.
Revocation of acceptance without appeal. Under section 50A, the Commissioner may revoke acceptance of a standard patent before grant, taking into account all circumstances existing at the time of acceptance even if unknown at that time. The decision is not appealable to the Federal Court (s 51), leaving judicial review as the only recourse and creating a period of acute uncertainty for applicants.
Computerised decisions and substitution. The interplay between an original computer‑generated decision, the Commissioner’s power to substitute it, and the ART’s review of the substituted decision (ss 223A, 224(1A)) raises novel procedural issues concerning finality and natural justice.
Gotchas
Several traps await the unwary practitioner.
Indefinite postponement of acceptance (s 49A(5)). If an applicant requests postponement and the Commissioner does not specify a day, the application sits indefinitely. The applicant must withdraw the postponement request in writing; failure to do so before the deadline prescribed under section 142(2)(e) causes the application to lapse.
Section 50A revocation of acceptance. Acceptance can be undone at any time before grant based on circumstances unknown at acceptance, with no appeal to the Federal Court. Delay between acceptance and grant amplifies the risk.
Innovation patent certification requirement. An innovation patent cannot be enforced unless certified. Sending a threat letter before certification will almost certainly be an unjustifiable threat (s 129A(1)-(2)), exposing the patentee to a claim for damages.
Amendments after acceptance or certification. Once the “relevant time” (acceptance for standard patents, certification for innovation patents) has passed, an amendment is not allowable if the claims would not in substance fall within the pre‑amendment scope or would breach section 40(2)-(3A) (s 102(2)). This restricts the ability to overcome validity attacks.
Prior use defence : derivation. The defence under section 119 is lost if the invention was derived from the patentee or predecessor, even indirectly, unless the derivation was from publicly available information disclosed during the section 24(1)(a) grace period. Practitioners must rigorously trace the origin of the prior use.
Crown exploitation : notice and terms. The 14‑day advance notice requirement under section 163(3)(e) is strict; failure to give it removes the immunity. Once terms are agreed or determined, any deviation constitutes infringement (ss 163(2), 163A(2)).
Legal practitioner trap. A legal practitioner must not prepare a specification or an amendment document unless acting under the instructions of a registered patent attorney or the amendment is directed by a court under section 105 (s 202). This restriction operates despite general rights of legal practice.
Incorporated patent attorneys : director absence. Failing to notify the Designated Manager within seven days of not having a patent attorney director, or carrying on business after that period without a director, is a strict liability offence attracting 150 penalty units (s 201B(1)-(2)).
Evidential burden for patent attorney exception defences. In a prosecution under section 201, the defendant bears the evidential burden for the exceptions concerning a deceased attorney’s business, employees and related company groups (Notes to s 201).
Five‑year prosecution window. The professional conduct offences in Part 2 of Chapter 20 can be prosecuted up to five years after the offence (s 204), far exceeding the usual 12‑month period.
Commissioner’s coercive powers : preconditions. A witness cannot be summoned, and documents cannot be required, unless the Commissioner is satisfied on the balance of probabilities that the person has a substantial interest in the proceedings and the evidence or documents are of substantial relevance (s 210(2), (4)).
Extensions of time : due care cap and intervening users. The “due care” extension under section 223(2A) can only be sought after the time has expired and is subject to a prescribed maximum period. If an extension of more than three months is granted, prescribed provisions operate for the protection or compensation of persons who exploited the invention during the lapse (s 223(9)), and no infringement proceedings can be brought for the gap period (s 223(10)).
Unregistered documents inadmissible to prove title. Section 196(1) provides that a document that has not been filed in the Register is not admissible in any proceedings to prove title to a patent or an interest, except in limited circumstances. This can be catastrophic for a party relying on an unregistered assignment or licence.
Process patent burden shift. Under section 121A, if a product is identical and it is very likely made by the patented process, and the patentee has taken reasonable but unsuccessful steps to discover the defendant’s process, the onus shifts to the defendant to prove a different process was used. The court must, however, consider the defendant’s legitimate interest in protecting manufacturing secrets.
Computerised decision substitution. The Commissioner may substitute a computer‑generated decision if satisfied it is incorrect. This means an initial automated decision has no finality until the substitution window closes and the person may need to monitor both the original output and any subsequent substitute.
Continuous charge requirement for patent attorney offices. A registered patent attorney must ensure an individual registered patent attorney is in “regular attendance” and “continuous charge” of patents work at each office (s 203), a requirement that demands practical attention to office staffing and structure.
How to comply
Compliance and protection strategies flow from the architecture described above.
Ensure proper registration and supervision for patent attorney services. If providing or receiving patent attorney services, confirm the practitioner or firm is appropriately registered on the Register of Patent Attorneys. Incorporated entities must maintain a patent attorney director. Legal practitioners must only prepare specifications under instruction from a registered patent attorney.
Maintain privilege carefully. To benefit from the statutory privilege under section 200, ensure communications are for the dominant purpose of obtaining “intellectual property advice” from a registered patent attorney. Advice of a purely scientific or technical nature falls outside the privilege.
Manage time limits and fees strictly. Diarise requests for examination, payment of continuation and renewal fees, and the lapsing deadlines. Where an extension of time is needed, document the steps taken so that a “due care” argument (s 223(2A)) can be mounted if the ordinary discretionary grounds are unavailable.
Monitor the status of innovation patents. Before sending any demand letter or commencing infringement proceedings, ensure the innovation patent has been examined and certified. Uncertified innovation patents cannot be enforced, and threats based on them are unjustifiable.
Draft and review specifications to meet section 40. Claims must be clear, succinct, supported by the description and not rely on references to drawings or descriptions unless absolutely necessary. For innovation patents, adhere to the five‑claim limit. If micro‑organisms are involved, comply with the deposit requirements in section 6 at filing.
Control the acceptance and amendment process. Avoid indefinite postponement of acceptance under section 49A(5) and, if used, diarise the withdrawal. After acceptance or certification, any amendment must not widen the claims. Consent from mortgagees and exclusive licensees is required before seeking leave to amend (s 103).
Protect prior use rights through provenance records. If a business relies on the prior use defence, document the independent origin of the product or process and confirm it was not derived from the patentee or a predecessor, or ensure it falls within the grace period disclosure exception (s 119(3)).
Manage Crown interactions proactively. If the Crown approaches for authorisation to use a patented invention, engage in negotiations and document attempts to agree reasonable terms. If the Crown proceeds under section 163, monitor the 14‑day notice requirement and ensure an agreement under section 165 is reached, as non‑compliance with that agreement is infringement.
Handle threats with care. Limit communications with potential infringers to factual notifications. Any statement that could be construed as an implied threat may found a cause of action under section 128.
File and register all dealings. Assignments, licences and security interests should be entered on the Register promptly. Section 196(1) renders unregistered documents inadmissible as proof of title, which can undermine enforcement efforts. PPSA security interests are handled separately but should also be perfected under the PPSA.
Plan for review and appeal. When facing an adverse Commissioner decision, check the list in section 224 to see whether a merits review application to the ART lies. For appealable decisions not listed there (or excluded like section 50A), consider Federal Court avenues. Ensure the decision notice contains a statement of review rights; its absence does not affect validity but may give tactical grounds for an extension of time.
Use the formalities instrument. The Commissioner’s instrument under section 229, published in the Official Journal, prescribes the detailed formalities requirements for patent requests and specifications. Before filing, consult the current instrument to avoid a rejection for non‑compliance.
Mark patented products. Substantial sale or use of products marked as patented creates a presumption of knowledge of the patent, which can defeat an innocent infringement defence (s 123(2)) and strengthen the claim for damages.
Novelty
(1) For the purposes of this Act, an invention is to be taken to be novel when compared with the prior art base unless it is not novel in the light of any one of the following kinds of information, each of which must be considered separately:
(a) prior art information (other than that mentioned in paragraph (c)) made publicly available in a single document or through doing a single act;
(b) prior art information (other than that mentioned in paragraph (c)) made publicly available in 2 or more related documents, or through doing 2 or more related acts, if the relationship between the documents or acts is such that a person skilled in the relevant art would treat them as a single source of that information;
(c) prior art information contained in a single specification of the kind mentioned in subparagraph (b)(ii) of the definition of prior art base in Schedule 1.
Inventive step
(2) For the purposes of this Act, an invention is to be taken to involve an inventive step when compared with the prior art base unless the invention would have been obvious to a person skilled in the relevant art in the light of the common general knowledge as it existed (whether in or out of the patent area) before the priority date of the relevant claim, whether that knowledge is considered separately or together with the information mentioned in subsection (3).
(3) The information for the purposes of subsection (2) is:
(a) any single piece of prior art information; or
(b) a combination of any 2 or more pieces of prior art information that the skilled person mentioned in subsection (2) could, before the priority date of the relevant claim, be reasonably expected to have combined.
Innovative step
(4) For the purposes of this Act, an invention is to be taken to involve an innovative step when compared with the prior art base unless the invention would, to a person skilled in the relevant art, in the light of the common general knowledge as it existed (whether in or out of the patent area) before the priority date of the relevant claim, only vary from the kinds of information set out in subsection (5) in ways that make no substantial contribution to the working of the invention.
(5) For the purposes of subsection (4), the information is of the following kinds:
(a) prior art information made publicly available in a single document or through doing a single act;
(b) prior art information made publicly available in 2 or more related documents, or through doing 2 or more related acts, if the relationship between the documents or acts is such that a person skilled in the relevant art would treat them as a single source of that information.
(6) For the purposes of subsection (4), each kind of information set out in subsection (5) must be considered separately.
[Notes: (1) For the meaning of document see section 2B of the Acts Interpretation Act 1901.
(2) See also the definitions of prior art base and prior art information in Schedule 1: see also paragraph 18(1)(b) and section 98.]
7A Meaning of useful
7A Meaning of useful
(1) For the purposes of this Act, an invention is taken not to be useful unless a specific, substantial and credible use for the invention (so far as claimed) is disclosed in the complete specification.
(2) The disclosure in the complete specification must be sufficient for that specific, substantial and credible use to be appreciated by a person skilled in the relevant art.
(3) Subsection (1) does not otherwise affect the meaning of the word useful in this Act.
9 Secret use
9 Secret use
For the purposes of this Act, the following acts are not to be taken to be secret use of an invention in the patent area:
(a) any use of the invention by or on behalf of, or with the authority of, the patentee or nominated person, or his or her predecessor in title to the invention, for the purpose of reasonable trial or experiment only;
(b) any use of the invention by or on behalf of, or with the authority of, the patentee or nominated person, or his or her predecessor in title to the invention, being use occurring solely in the course of a confidential disclosure of the invention by or on behalf of, or with the authority of, the patentee, nominated person, or predecessor in title;
(c) any other use of the invention by or on behalf of, or with the authority of, the patentee or nominated person, or his or her predecessor in title to the invention, for any purpose other than the purpose of trade or commerce;
(d) any use of the invention by or on behalf of the Commonwealth, a State, or a Territory where the patentee or nominated person, or his or her predecessor in title to the invention, has disclosed the invention, so far as claimed, to the Commonwealth, State or Territory;
(e) any use of the invention by or on behalf of, or with the authority of, the patentee or nominated person, or his or her predecessor in title to the invention, for any purpose, if a complete application is made for the invention within the prescribed period.
[Note: See also paragraph 18(1)(d)]
10 Certain international applications to be taken to have been given an international filing date
10 Certain international applications to be taken to have been given an international filing date
(1) Where:
(a) an international application specifies Australia as a designated State under Article 4(1)(ii) of the PCT; and
(b) the receiving Office does not give the application an international filing date; and
(c) the Commissioner is satisfied, on the balance of probabilities, that the application should, under Article 25(2)(a) of the PCT, be treated as if it had been given an international filing date;
the application is to be taken, for the purposes of this Act, to have been given an international filing date under Article 11 of the PCT.
(2) This section does not apply to an international application that was not filed in the receiving Office in English unless the following documents have been filed:
(a) a translation of the application into English;
(b) if required by the regulations—a certificate of verification (within the meaning of the regulations) of the translation.
(3) Where this section applies, the international filing date of the application is to be taken to be the date that, in the opinion of the Commissioner, should have been given to the application as its international filing date under the PCT.
[Note: international filing date is defined in Schedule 1.]
11 Act binds the Crown
11 Act binds the Crown
(1) This Act binds the Crown in right of the Commonwealth, of each of the States, of the Australian Capital Territory and of the Northern Territory.
(2) Nothing in this Act makes the Crown liable to be prosecuted for an offence.
12 Application of Act
12 Application of Act
This Act extends to:
(a) each external Territory; and
(b) the Australian continental shelf; and
(c) the waters above the Australian continental shelf; and
(d) the airspace above Australia, each external Territory and the Australian continental shelf.
12A Application of the Criminal Code
12A Application of the Criminal Code
Chapter 2 of the Criminal Code applies to all offences created by this Act.
Note: Chapter 2 of the Criminal Code sets out the general principles of criminal responsibility.
Chapter 2—Patent rights, ownership and validity
Part 1 Patent rights
Part 1—Patent rights
13 Exclusive rights given by patent
13 Exclusive rights given by patent
(1) Subject to this Act, a patent gives the patentee the exclusive rights, during the term of the patent, to exploit the invention and to authorise another person to exploit the invention.
(2) The exclusive rights are personal property and are capable of assignment and of devolution by law.
(3) A patent has effect throughout the patent area.
14 Assignment of patent
14 Assignment of patent
(1) An assignment of a patent must be in writing signed by or on behalf of the assignor and assignee.
(2) A patent may be assigned for a place in, or part of, the patent area.
Part 2 Ownership
Part 2—Ownership
15 Who may be granted a patent?
15 Who may be granted a patent?
(1) Subject to this Act, a patent for an invention may only be granted to a person who:
(a) is the inventor; or
(b) would, on the grant of a patent for the invention, be entitled to have the patent assigned to the person; or
(c) derives title to the invention from the inventor or a person mentioned in paragraph (b); or
(d) is the legal representative of a deceased person mentioned in paragraph (a), (b) or (c).
(2) A patent may be granted to a person whether or not he or she is an Australian citizen.
16 Co‑ownership of patents
16 Co‑ownership of patents
(1) Subject to any agreement to the contrary, where there are 2 or more patentees:
(a) each of them is entitled to an equal undivided share in the patent; and
(b) each of them is entitled to exercise the exclusive rights given by the patent for his or her own benefit without accounting to the others; and
(c) none of them can grant a licence under the patent, or assign an interest in it, without the consent of the others.
(2) Where a patented product, or a product of a patented method or process, is sold by any of 2 or more patentees, the buyer, and a person claiming through the buyer, may deal with the product as if it had been sold by all the patentees.
(3) This section does not affect the rights or obligations of a trustee or of the legal representative of a deceased person, or rights or obligations arising out of either of those relationships.
17 Directions to co‑owners
17 Directions to co‑owners
(1) Where there are 2 or more patentees, the Commissioner may, on the application of any of them, give such directions in accordance with the application as the Commissioner thinks fit, being directions about:
(a) a dealing with the patent or an interest in it; or
(b) the grant of licences under the patent; or
(c) the exercise of a right under section 16 in relation to the patent.
(2) If a patentee fails to do anything necessary to carry out a direction under subsection (1) within 14 days after being asked in writing to do so by one of the other patentees, the Commissioner may, on the application of one of those other patentees, direct a person to do it in the name and on behalf of the defaulting patentee.
(3) Before giving a direction, the Commissioner must give an opportunity to be heard:
(a) in the case of an application by a patentee or patentees under subsection (1)—to the other patentee or patentees; and
(b) in the case of an application under subsection (2)—to the defaulting patentee.
(4) The Commissioner must not give a direction that:
(a) affects the rights or obligations of a trustee or of the legal representative of a deceased person, or rights or obligations arising out of either of those relationships; or
(b) is inconsistent with the terms of an agreement between the patentees.
Part 3 Validity
5 Associated applications
For the purposes of this Act, a complete application is to be taken to be associated with a provisional application if, and only if, the patent request filed in respect of the complete application identifies the provisional application and contains a statement to the effect that the applications are associated.
[Note: see sections 29 and 38]
6 Deposit requirements
For the purposes of this Act, the deposit requirements are to be taken to be satisfied in relation to a micro‑organism to which a specification relates if, and only if:
(a) the micro‑organism was, on or before the date of filing of the specification, deposited with a prescribed depositary institution in accordance with the rules relating to micro‑organisms; and
(b) the specification includes, at that date, such relevant information on the characteristics of the micro‑organism as is known to the applicant; and
(c) at all times since the end of the prescribed period, the specification has included:
(i) the name of a prescribed depositary institution from which samples of the micro‑organism are obtainable as provided by the rules relating to micro‑organisms; and
(iii) the file, accession or registration number of the deposit given by the institution; and
(d) at all times since the date of filing of the specification, samples of the micro‑organism have been obtainable from a prescribed depositary institution as provided by those rules.
[Note: see sections 41 and 42]
7 Novelty, inventive step and innovative step
Novelty
(1) For the purposes of this Act, an invention is to be taken to be novel when compared with the prior art base unless it is not novel in the light of any one of the following kinds of information, each of which must be considered separately:
(a) prior art information (other than that mentioned in paragraph (c)) made publicly available in a single document or through doing a single act;
(b) prior art information (other than that mentioned in paragraph (c)) made publicly available in 2 or more related documents, or t
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