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PatentBrief

Post-Grant Challenges

Patent Opposition

EPO opposition within 9 months of grant can revoke a patent across 44 countries — the most cost-effective way to challenge a European patent.

FAQ

What are EPO opposition proceedings and how do they work?

EPO opposition is the primary mechanism for challenging European patents after grant: LEGAL BASIS: Article 99-105 EPC (European Patent Convention); TIMING: any third party (including competitors, industry groups, or anonymous third parties) can file an opposition within 9 months of the publication of the grant of the European patent; GROUNDS FOR OPPOSITION: Article 100 EPC — only three grounds: (a) lack of novelty or inventive step (prior art): the most common ground; (b) insufficient disclosure (enablement failure): the application doesn't enable a POSITA to reproduce the invention; (c) extension beyond original disclosure: the granted claims or description were extended beyond the content of the original application (added subject matter); NOTE: unlike US IPR, EPO oppositions can include Art. 100(c) added matter challenges; PROCEDURE: opposition is filed with the EPO Opposition Division (three technically qualified examiners); observation period: patent owner responds; typically 12-24 months to first written decision; POSSIBLE OUTCOMES: patent MAINTAINED AS GRANTED; patent MAINTAINED IN AMENDED FORM (proprietor proposes amendments to overcome the opposition); patent REVOKED (the entire patent is invalidated); APPEAL: either party can appeal to the EPO Technical Board of Appeal (TBA); TBA decisions are final and binding; third-level appeal to the Enlarged Board of Appeal for important legal questions; GEOGRAPHIC SCOPE: if the EPO revokes a European patent, the revocation applies to ALL member states in which the patent was validated; this is extremely powerful — one proceeding can invalidate protection across 44 member states; COST: opposition filing fee ~€880; attorney fees €10,000-€50,000+ through oral proceedings; much cheaper than litigating separately in each European country; ANONYMITY: oppositions can be filed 'in the name of' a third party through a straw-man opposition attorney; the true opponent's identity need not be revealed.

How does US inter partes review compare to EPO opposition?

Inter partes review is the primary US mechanism for challenging issued patents at the USPTO: LEGAL BASIS: 35 U.S.C. §§ 311-319; created by the America Invents Act (AIA); effective September 16, 2012; TIMING: must be filed within 1 year after service of a complaint alleging infringement; no general 9-month window (unlike EPO); if no infringement complaint has been filed, can file at any time during the patent term; GROUNDS: only § 102 (novelty) and § 103 (obviousness) based on patents or printed publications; § 101 and § 112 grounds CANNOT be raised in IPR (unlike EPO opposition); INSTITUTION THRESHOLD: 'reasonable likelihood that the petitioner would prevail on at least 1 challenged claim'; about 60-70% of IPR petitions are instituted; PROCEDURE: three-member panel of Administrative Patent Judges (APJs) at PTAB; one year from institution to final written decision (FWD); DISCOVERY: limited — depositions of declarants only; no document requests or interrogatories; oral hearing optional but typical; ESTOPPEL: after FWD, petitioner estopped from asserting invalidity in district court or ITC on any ground that was raised OR COULD HAVE BEEN RAISED in IPR; COST: USPTO fees $19,000-$25,000; attorney fees $50,000-$200,000+; OUTCOME: FWD cancels all, some, or none of the challenged claims; certificate of unpatentability issued for canceled claims; STATISTICS: approximately 45-50% of all claims that reach FWD are canceled; EPO vs. IPR: EPO: 9-month window; all grounds; covers all EP states; appeals within EPO; cheaper; IPR: 1-year bar from complaint; § 102/§ 103 only; covers US only; PTAB + Federal Circuit appeals; more expensive; faster timeline (12 months).

What is post-grant review and how does it differ from IPR?

Post-grant review (PGR) is a broader but narrowly time-limited post-issuance challenge: LEGAL BASIS: 35 U.S.C. §§ 321-329; available for patents with ANY claim having an effective filing date on or after March 16, 2013 (AIA first-inventor-to-file patents); TIMING: must be filed within 9 months of the patent's grant or reissuance; after 9 months, only IPR is available (limited to § 102/§ 103); GROUNDS: MUCH BROADER than IPR: any ground of invalidity under § 101 (eligibility), § 102 (novelty), § 103 (obviousness), § 112 (specification requirements), and any other ground; this is the same scope as EPO opposition grounds; INSTITUTION THRESHOLD: 'more likely than not that at least 1 of the challenged claims is unpatentable'; slightly higher than IPR's 'reasonable likelihood' standard; PROCEDURE: same PTAB panel as IPR; 12-month timeline to FWD; ESTOPPEL: after FWD, petitioner estopped from raising in district court any ground raised or reasonably could have been raised in PGR; STRATEGIC USE: PGR is ideal for challenging: § 101 eligibility (Alice/Mayo challenges); written description and enablement (§ 112); newly issued patents before competitors design around; COVERED BUSINESS METHOD REVIEW (CBM): a special PGR-like proceeding for financial product/service patents; originally created by AIA; SUNSET: CBM petitions could only be filed before September 16, 2020 — now expired; any CBM patent can still be challenged via IPR (§ 102/§ 103) or PGR (within 9 months of grant); TIMING TRAP: missing the 9-month PGR window and being served with an infringement complaint within 1 year = ONLY IPR available; § 101/§ 112 challenges must then be pursued in district court (more expensive).

When should a company use EPO opposition vs. US IPR vs. district court to challenge a patent?

Patent challenge strategy requires selecting the right forum for each situation: EPO OPPOSITION — BEST WHEN: patent recently granted (within 9 months); patent covers the European market; patent has clear prior art or added matter issues; budget is limited (EPO opposition is very cost-effective per country covered); the company wants to destroy the patent across all of Europe in a single proceeding; challenging validity early before significant infringement damages accumulate; US IPR — BEST WHEN: within 1 year of service of infringement complaint (or proactively before being sued); strong prior art exists (patents or printed publications); the 35-page petition limit allows complete presentation of the strongest arguments; looking for faster resolution (12 months) than district court litigation; using IPR as part of a 'dual track' strategy (IPR + district court invalidity defense running simultaneously); CAUTION: IPR estoppel is broad — all grounds that COULD have been raised; must account for prior art searches before filing; US DISTRICT COURT — BEST WHEN: § 101 eligibility is the primary invalidity argument (cannot be raised in IPR); § 112 challenges are strongest (can be raised in PGR but not IPR; district court has no IPR-timing limit); IPR is time-barred (more than 1 year after complaint); the company can fund full litigation; the company wants a jury decision; COMBINED STRATEGY: file IPR immediately after being served with complaint (within 1 year); simultaneously assert invalidity in district court (§ 101/§ 112/other grounds not available in IPR); attempt to stay district court litigation pending IPR outcome; request is often granted (reduces court workload); COST COMPARISON: EPO opposition: €15,000-€60,000+; US IPR: $70,000-$250,000+; US district court invalidity defense: $1M-$5M+; UK/Germany invalidity: £50,000-£200,000+.

What are the grounds for EPO opposition and how does the opposition division evaluate them?

EPO opposition grounds are more limited but different from US proceedings: GROUND 1 — LACK OF NOVELTY OR INVENTIVE STEP (Article 100(a)): most common ground; based on prior art that was not considered during examination; prior art can include: patents from any country; academic publications; prior use or disclosure (must be sufficiently documented); NOVELTY ANALYSIS: the same EPO novelty test (Article 54): a single disclosure disclosing every claimed feature; prior art not limited to published documents (public prior use also counts); INVENTIVE STEP ANALYSIS: EPO problem-solution approach; identify closest prior art; formulate objective technical problem; could/would analysis; secondary evidence (unexpected technical effects); GROUND 2 — INSUFFICIENCY OF DISCLOSURE (Article 100(b)): the European specification was insufficient for a skilled person to carry out the invention; equivalent to US § 112 enablement; requires clear and convincing evidence that POSITA cannot make/use the invention; GROUND 3 — ADDED MATTER (Article 100(c)): the patent's claims or description were extended beyond the content of the application as originally filed; this is similar to US § 132 new matter prohibition but applies to granted claims; a claim limitation was changed to be broader or narrower without basis in the original application; 'intermediate generalization': adding a specific feature from an example to a broader claim without adequate basis; COMBINATION OF GROUNDS: most successful oppositions use ground 1 (novelty/inventive step) with supporting grounds; ground 3 (added matter) is sometimes the most decisive — if a claim was broadened during prosecution without basis, it can be revoked; BURDEN OF PROOF: opponent bears the burden of proving invalidity; claim construction is done objectively by the Division; AUXILIARY REQUESTS: patent owner can submit multiple auxiliary requests (amended claim sets) to be considered if the main request fails.

Related Guides

Inter Partes ReviewPost-Grant ReviewInventive Step (EPO)International FilingPatent Invalidity