We explore some of the key updates by topic below.
The Guidelines introduce a change of practice regarding the assessment of novelty for selection inventions (G-VI, 7 and G-VII, 12).
The previous tests—"seriously contemplate" for individual selections and "narrow and sufficiently far removed" for sub-ranges—have been abandoned. In their place, the Guidelines adopt the "gold standard": a sub-range is novel if it cannot be established that the skilled person, using common general knowledge, can directly and unambiguously derive the selected sub-range from the prior art (G 2/10, T 1688/20).
The Guidelines have been amended in view of decision G 1/23, with key updates to prior art and enabling disclosure (G-IV, 2 and G-IV, 7.2.1).
The updated guidance confirms:
New guidance on novelty assessment for Article 54(5) claims, including a dedicated F-III, 10. Key new subsections clarify when prior art is novelty-destroying: G-VI, 6.1.2.1 addresses preclinical data and clinical trials (mere announcement of a clinical trial without positive results may not destroy novelty); G-VI, 6.1.2.2 covers patient group definitions (a different patient sub-group characterised by biomarkers, age, etc. may represent a new specific use); and G-VI, 6.1.2.3 addresses mechanistic definitions leading to new clinical situations.
The Guidelines have been amended in view of decision G 1/24, with key updates to claim interpretation principles (F-IV, 4.2) and consequential changes at the search stage (B-III, 3.2).
The updated guidance confirms that:
Part F, Chapter IV has been updated with:
Following OJ EPO 2025, A49 and A57, the Guidelines now address the processing of colour drawings across multiple sections. Key updates include:
The Programme for Accelerated Prosecution of European Patent Applications (PACE) has been abolished for the search phase (E-VIII, 4). Accelerated search is no longer available, as reflected in amendments to A-XI, 2.3 referencing OJ EPO 2025, A69. PACE remains available for examination.
The Guidelines now provide important clarifications on how divisions must exercise their discretion when admitting or refusing amendments.
Examination (H-II, 2.3): When exercising discretionary power not to admit amendments, the Examining Division must give reasons as to why the amended claims are prima facie not allowable. Importantly, if the reasons for refusing a request require the same detailed discussion as would be needed had the request been admitted, then that request should be admitted. An extensive reasoning as to why amended claims are not allowable is not compatible with a prima facie assessment.
Opposition (E-VI, 2.2.1): The Opposition Division must first review the contents of an auxiliary request when considering whether to refuse it. This ensures an assessment is made as to whether the request is a fair attempt at overcoming objections, and whether it is prima facie allowable.
Postponement for New Objections (E-III, 8.11.1): Where new and major objections are raised during oral proceedings, and the applicant or proprietor cannot reasonably be required to make the necessary amendments there and then, a request for postponement or to continue proceedings in writing shall be granted.
Repeated Amendment Requests After Rule 71(3) (C-V, 4.10): New guidance on the procedure to be followed when applicants repeatedly request amendments in reply to communications under Rule 71(3) (text intended for grant). The Guidelines now detail when a summons to oral proceedings must be issued and when the application can be refused immediately.
Euro-PCT procedural guidance has been reorganised: Part E, Chapter IX content has moved to new Chapters A-XII to A-XV, consolidating all formalities examination within Part A.
A new General Part, Section 5 addresses the use of artificial intelligence. The EPO has adopted a clear principle: parties are responsible for the content of their patent applications and submissions regardless of whether a document has been prepared with the assistance of an AI tool - mirroring the position taken by the epi in their guidelines on generative AI.
This builds upon the preliminary guidance introduced in 2025, which first acknowledged AI tool usage. The 2026 update goes further—the EPO now has a dedicated section rather than a passing reference, and confirms that AI "can improve the quality and efficiency" of its own work while committing to a "human-centric approach" governed by its formal AI policy.
Additionally, the EPO has introduced AI-assisted minute-taking for oral proceedings (E-III, 10.1). Sound recordings are now made when minutes of oral proceedings held by videoconference before examining and opposition divisions are drawn up with AI assistance. These recordings are deleted once the minutes are issued to the parties, and copies of the recordings are not provided to parties. This follows a successful pilot phase—for more detail, see our previous coverage of the EPO's AI-assisted minute-taking initiative.
The EPO's recognition that AI "can improve the quality and efficiency" of patent work reflects a growing consensus across the profession - from the epi to major law firms and in-house teams worldwide.
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The 2026 Guidelines enter into force in April 2026. The binding version will be published on the EPO website in both HTML and PDF formats, with modifications viewable via the "Show modifications" feature. This article provides a general overview and does not constitute legal advice. Readers should consult qualified professionals before acting on any of the information presented.
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