International Patents · IP Australia
Australia Patent
IP Australia grants standard patents under the Patents Act 1990, with a 20-year term and examination standards significantly raised by the 2013 Raising the Bar reforms. The innovation patent was abolished in 2021. Pharmaceutical patents benefit from an Extension of Term of up to 5 additional years for TGA regulatory delay.
Patent authority
IP Australia (IPAUSTRALIA)
Standard patent term
20 years from filing date
Examination request deadline
5 years from filing (or lapse)
PCT national phase
31 months from priority date
Extension of Term (pharma)
Up to 5 years; ≤ 25 years from grant
Innovation patent
Abolished August 26, 2021
Examination Process
The IP Australia standard patent process
Filing
Applications are filed with IP Australia (Australia's patent, trademark, and designs office). A standard patent application can be filed directly, or — more commonly for international filers — entered via the PCT national phase (deadline: 31 months from earliest priority date). Patent applications must be in English. Filing fee: AU$370 for standard patent application (electronic); AU$1,710 for comprehensive first stage for applications with more than 20 claims (additional claim fees apply).
Publication
Applications are published 18 months from the earliest priority date (same as EPO/JPO/USPTO). After publication, the application is open for public inspection (OPI). Pre-grant opposition can be filed within 3 months of acceptance advertisement — NOT at publication. There is no inter partes proceeding at the publication stage.
Request for examination
An examination request must be filed within 5 years of the filing date. If no request is filed within 5 years, the application lapses (automatic). The examination request fee is AU$490 (electronic). IP Australia offers a 'deferred examination' pathway — applicants can delay requesting examination for up to 5 years to assess commercial viability. PPH (Patent Prosecution Highway) is available: if a US, EPO, KIPO, JPO, or other PPH-participating office has allowed claims, Australian examination can be accelerated using the corresponding allowed claims as the basis.
Examination
The examiner conducts a prior art search and issues a First Examination Report (FER) raising objections under the Patents Act 1990. Common rejections include: lack of novelty (s. 18(1)(a)), lack of inventive step (s. 18(1)(b)), insufficient support/enablement (s. 40), fair basis objections. Response due within 21 months of the filing date (or within 12 months from the FER, whichever gives more time). Additional examination reports (AERs) may be issued. Examiners have significant latitude to conduct further searches.
Acceptance and opposition
When examination is successfully completed, IP Australia issues a Notice of Acceptance and advertises the acceptance in the Australian Official Journal of Patents. A 3-month opposition window opens from the date of advertisement. Any person may oppose the grant of the patent during this window by filing a Statement of Grounds and Particulars. IP Australia conducts the opposition hearing (unlike Australia's court-based revocation, which goes to the Federal Court). Opposition grounds include lack of novelty, inventive step, or utility; false suggestion; and improper obtaining. If no opposition is filed (or opposition fails), the patent is granted.
Grant and renewal
The standard patent grants after the opposition period expires without opposition (or after a failed opposition). The patent term is 20 years from the filing date. Annual renewal fees are due from Year 5 onward. Fees increase each year: AU$300 (Year 5) rising to approximately AU$1,800 (Year 20). Pharmaceutical patents may apply for an Extension of Term (EoT) of up to 5 years — application must be made within 6 months of TGA approval of the pharmaceutical substance.
Raising the Bar Reforms
The Raising the Bar Act 2012 — key changes for applications filed from April 15, 2013
Prior art base expanded
Before Raising the Bar (pre-April 15, 2013 applications): the prior art base for inventive step was limited to documents 'published in the patent area' — essentially Australia plus major patent offices. After Raising the Bar: the prior art base aligns with international standards — any published document worldwide is relevant to inventive step analysis (s. 7(3)). This significantly raised the bar for what constitutes an inventive step in Australia.
Sufficiency/enablement raised
Before Raising the Bar: specifications only needed to 'describe' the invention. After Raising the Bar: the full scope of the claims must be 'fully enabled' — aligning with UK/EPO enablement standards. The key decision is Idenix Pharmaceuticals LLC v Gilead Sciences Pty Limited [2019] FCAFC 237 — the Full Federal Court applied the post-Raising the Bar enablement standard to functional genus claims for HCV treatment, finding claims covering millions of compounds were not enabled by the specification's examples. This mirrors the US Amgen v. Sanofi result at the Supreme Court.
Grace period refined
The Raising the Bar Act refined the 12-month grace period under s. 24(1). Disclosures by or with the consent of the applicant within 12 months of filing are protected. However, the grace period requires that the disclosure must have been 'publicly available' — disclosures under confidentiality agreements that are not publicly available are not grace-period disclosures and can still constitute prior art. Best practice remains: file before disclosing.
Key Differences
Australia vs United States — key patent law differences
| Dimension | Australia (IP Australia) | United States (USPTO) |
|---|---|---|
| Patent term | 20 years from filing date (standard patent). Extensions of time (EOT) available for pharmaceutical patents for regulatory delay — up to 5 additional years. | 20 years from earliest effective US filing date. Patent Term Adjustment (PTA) for USPTO delays. Patent Term Extension (PTE, § 156) for pharma. |
| Grace period | 12 months (s. 24(1)(a) Patents Act 1990) for the applicant's own disclosures. CRITICAL: this grace period was narrowed by the Raising the Bar Act 2012 to exclude certain disclosures that were not made publicly available in the ordinary course of business. | 12 months under AIA (§ 102(b)(1)) for applicant's own disclosures. Pre-AIA: 12 months for any disclosure anywhere. |
| Inventive step test | Two-step test: (1) determine the common general knowledge (CGK) of the relevant skilled addressee; (2) ask whether the invention would have been obvious to that person. Post-Raising the Bar: information from any published document worldwide (not just Australian) can be combined with CGK for inventive step analysis — aligning closer to US § 103 standard. | Graham v. John Deere four-factor framework; KSR flexible obvious-to-try standard; TSM no longer required but still relevant. |
| Innovation patents | ABOLISHED from August 26, 2021 (IP Laws Amendment (Productivity Commission Response Part 2) Act 2020). Innovation patents were a second-tier patent for minor innovations: 8-year term, 'innovative step' (lower than inventive step — any novel, micro-contribution qualifies), self-certification at filing, substantive examination only when certified for enforcement. No new innovation patent applications accepted after August 26, 2021; existing innovation patents remain valid for their term. | No equivalent second-tier patent system. Utility patents require full inventive step. Provisional applications serve a comparable 'placeholder' function but require a full utility application within 12 months. |
| Examination request | Required within 5 years of the filing date (or 2 years from filing in some cases). If no request is filed, the application lapses. | Examination is automatic — no separate request required. |
| Continuation practice | No continuation applications in the US sense. Divisionals are available. Divisionals must be filed before the parent is accepted (accepted = allowed). Claims must be consistent with the parent specification. | Continuation (CON), continuation-in-part (CIP), and divisional (DIV) applications available. Continuation can be filed any time while parent is pending. |
| Opposition proceedings | Pre-grant opposition: any person can oppose an accepted application within 3 months of acceptance advertisement. Post-grant revocation: via Federal Court of Australia or IP Australia (re-examination). | No pre-grant opposition. Post-grant: IPR/PGR at PTAB (first 9 months for PGR, any time for IPR), or district court invalidity. |
| Pharmaceutical extensions | Extension of Term (EoT) under s. 70–79H Patents Act 1990: available if first pharmaceutical disclosure (TGA approval) occurred within 20 years of patent grant; maximum extension = 5 years; remaining term capped at 25 years from patent grant. Application must be made within 6 months of TGA approval of the pharmaceutical substance. | Patent Term Extension (PTE) under 35 U.S.C. § 156. Formula: ½ × IND clinical period + full FDA review; max 5 years; remaining term capped at 14 years after approval; one patent per NDA/BLA; 60-day deadline from FDA approval. |
Key Cases
Landmark Australian patent decisions
D'Arcy v Myriad Genetics Inc
[2015] HCA 35 (High Court of Australia)
Isolated naturally-occurring gene sequences (BRCA1 and BRCA2 mutations associated with breast/ovarian cancer risk) are NOT patent-eligible subject matter in Australia. The majority held that the isolated DNA sequences were not a 'manner of manufacture' under s. 18(1)(a) of the Patents Act because they fell within the exception for naturally-occurring subject matter — despite being isolated and purified in the laboratory. The High Court unanimously reversed the Full Federal Court's earlier decision allowing such claims. This case is Australia's equivalent of the US Myriad decision (Association for Molecular Pathology v. Myriad Genetics, S.Ct. 2013), which also held isolated genomic DNA ineligible.
Idenix Pharmaceuticals LLC v Gilead Sciences Pty Ltd
[2019] FCAFC 237 (Full Federal Court of Australia)
Applied the post-Raising the Bar enablement standard (s. 40(2)(a)) to a broad functional genus claim covering nucleoside compounds for treating HCV (Hepatitis C). The Full Federal Court found that the patent specification did not enable the full scope of the claimed genus — thousands of claimed compounds were not shown to work by the specification's examples, and the skilled addressee could not work the full scope without undue experimentation. This established Australia's modern enablement doctrine and aligned it closely with the EPO/UK sufficiency standard, foreshadowing what the US Supreme Court would hold in Amgen v. Sanofi (2023).
Sigma Pharmaceuticals v Wyeth
[2011] FCAFC 132 (Full Federal Court of Australia)
Found that the Extended Release venlafaxine formulation patent was invalid for lack of inventive step, even though the specific formulation was commercially successful. An important case illustrating that commercial success in Australia is considered as a secondary consideration for inventive step but does not override clear obviousness findings. Also illustrates Australia's pharmaceutical patent litigation landscape — generic drug companies commonly challenge pharma patents at the Full Federal Court level.
FAQ
Frequently asked questions
How long does Australian patent examination take?
Australian patent examination timelines depend on whether examination is expedited and on the technology area. Standard examination: after an examination request is filed, IP Australia typically issues a First Examination Report (FER) within 12–18 months from the examination request date. The total time from filing to grant for a standard patent without opposition is approximately 3–5 years. Expedited examination: IP Australia offers expedited examination for a fee of AU$2,000 — this accelerates the FER issuance to approximately 3–6 months. PPH (Patent Prosecution Highway) examination: if the USPTO or another PPH partner has allowed corresponding claims, Australian examination can be accelerated using those allowed claims as the basis. PPH applications typically receive a FER within 3–6 months. IP Australia accelerated examination for urgent commercial reasons: available on request with written justification (e.g., actual commercial working of the invention, impending litigation), no additional fee. The 5-year deadline for examination request is absolute — applications that do not receive an examination request within 5 years of filing automatically lapse.
What happened to the Australian innovation patent?
The innovation patent was a second-tier Australian patent designed to protect minor innovations that would not reach the inventive step required for a standard patent. Key characteristics: 8-year maximum term; 'innovative step' standard (defined as any new and innovative step, which was a much lower threshold than inventive step — essentially any contribution not previously known); self-certification at filing (no upfront examination); substantive examination only triggered when the patent owner sought to certify the patent for enforcement purposes. The innovation patent was abolished by the IP Laws Amendment (Productivity Commission Response Part 2) Act 2020, which came into force on August 26, 2021. No new innovation patent applications are accepted after August 26, 2021. This followed a recommendation by the Productivity Commission's 2016 IP review, which found that the innovation patent system primarily benefited existing patent holders and litigation defendants rather than stimulating actual innovation by small businesses. Impact on practitioners: existing innovation patents remain valid for their stated term. Practitioners are now focusing exclusively on standard patents for Australian protection. The loss of the innovation patent system means Australian law no longer offers a quick-registration, low-threshold option for protecting minor improvements.
Are software patents allowed in Australia?
Software and computer-implemented inventions are potentially patentable in Australia, but the legal position is nuanced. The 'manner of manufacture' requirement under s. 18(1)(a) of the Patents Act 1990 is the key eligibility hurdle, and the High Court has not definitively ruled on software in general. The leading case is Research Affiliates LLC v Commissioner of Patents [2014] FCAFC 150, where the Full Federal Court found that a purely mathematical method implemented on a computer was not patent-eligible — if the claimed invention is a scheme, plan, or abstract idea, implementation on a computer does not automatically make it eligible. However, computer-implemented inventions with a 'concrete, tangible, physical, or observable effect' in the computer itself, or which solve a technical problem in a technical way, are generally eligible. IP Australia's 2019 Examination Guidelines for computer-implemented inventions indicate that claims may be eligible if they produce a 'useful, concrete, and tangible result.' Practically: claims directed to improved computer functioning, new computer architectures, or specific technical applications of computing (robotics, signal processing, database management) are well-accepted. Pure business method claims or pure mathematical algorithm claims, even when claimed as implemented on a computer, face Alice/Mayo-equivalent scrutiny in Australia and are high-risk. The Australian position is broadly aligned with — but somewhat more permissive than — the post-Alice USPTO § 101 analysis.
What is an Extension of Term in Australia?
An Extension of Term (EoT) under sections 70–79H of the Patents Act 1990 is Australia's equivalent of the US Patent Term Extension (PTE) — it compensates pharmaceutical patent owners for time lost during TGA (Therapeutic Goods Administration) regulatory approval. Requirements: (1) The patent must be a standard patent for a pharmaceutical substance per se, or a method of use or composition of matter claim covering the substance; (2) The pharmaceutical substance (or a substance that contains the patented substance as an active ingredient) must have first been included in the Australian Register of Therapeutic Goods (ARTG) within 20 years of the grant of the patent; (3) The application for EoT must be made within 6 months of the first inclusion in the ARTG (this is a STRICT deadline — no extensions). How much extension: the EoT extends the patent term by the period from the patent's filing date to the date the first ARTG inclusion occurred, minus 5 years. The maximum extension is 5 years. The remaining patent term after the EoT cannot exceed 25 years from the date of the patent grant. Interaction with generic entry: generic drug companies routinely challenge EoT applications and the underlying patents at IP Australia via oppositions. If the EoT is granted, the generic company is blocked from marketing the drug for the extended period (subject to regulatory exclusivity separately). Key difference from US PTE: Australia's EoT calculation is simpler (filing to ARTG inclusion minus 5 years, capped at 5); the US formula is more complex (½ × IND period + FDA review period). Australia also allows EoT for subsequent ARTG inclusions in some circumstances.
How does Australia's inventive step test differ from the US obviousness standard?
Australia's inventive step test under s. 7(2) of the Patents Act 1990 and the US § 103 obviousness standard share the same ultimate question — would the invention have been obvious to a person skilled in the relevant art? — but differ in approach and application. Australia's two-step inventive step test: (1) Determine the common general knowledge (CGK): what would a skilled addressee have known without conducting a specific search — textbook knowledge, routine experimental practices, and generally known information in the field (but NOT information only discoverable by a specific targeted search); (2) Determine whether the claimed invention was obvious: would the skilled addressee, equipped with the CGK and the content of any applicable prior art document(s), have taken the step to reach the invention without inventive ingenuity? Post-Raising the Bar reforms: before April 2013, the prior art base for inventive step was limited to published documents in Australia and a handful of major patent databases. After the Raising the Bar Act 2012 (applying to applications filed from April 15, 2013), the prior art base for inventive step was expanded to include any published document worldwide — aligning with international standards. Key differences from US § 103: (1) No KSR 'flexible obvious to try' standard in Australian law — the obvious-to-try approach exists but requires a reasonable expectation of success with a finite number of identified candidates; (2) No formal 'secondary considerations' framework comparable to Graham v. John Deere — but commercial success, long-felt need, and failure of others are relevant; (3) Australia does not apply an 'analogous art' limitation in the same way as US pre-KSR TSM — post-Raising the Bar, any worldwide document may form the basis of an inventive step attack; (4) Common general knowledge plays a larger role in Australian inventive step than in US obviousness — CGK is the baseline from which the gap to the invention is measured; documents may be combined only with CGK or with a single document plus CGK, not freely combined with each other.
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