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Transatlantic Toolkit

Introducing our collection of quick tips and suggestions dedicated to helping US attorneys navigate UK and European patents, designs and the UPC.

Below you’ll find our developing list of tips specifically designed with the considerations of US attorneys in mind, aiming to help inform your high-level strategy decisions and assist you advising your clients.

We want this resource to be as collaborative and useful as possible, so please contact Olivia Crawford and Oliver Poskett with any comments, suggestions, and topics you want addressed, or questions you might have.

If these brief pointers prompt a deeper or client-specific consideration, we would be glad to hear from you directly to provide our input.

This page will be updated regularly, so bookmark it for ease of access and follow us on LinkedIn to see each update as it goes out.

 

Patents

Is your client concerned about the cost of filing an EP application in view of a negative International Search Report?

Consider filing a Demand for PCT Chapter II Examination at the EPO in the international phase. This provides applicants an additional bite of the cherry: an opportunity to submit amendments and arguments to the EPO before fully committing to the regional phases.

Further, if the EPO was ISA as well as IPEA, applicants enjoy a significant 75% reduction in the EPO’s examination fee – an effective discount of over $1,500 in Fall 2023.

Is your client concerned about the cost of renewal fees for an EP application, and is primarily interested in the UK market?

Consider filing in the UK directly: the UK fees are much lower and kick in later. The following figures are based on exchange rates in Fall 2023:

EPO renewal fees by year

  • 3rd year: $570
  • 4th year: $710
  • 5th year: $1000
    • Total up to year 5: $2,280

UKIPO renewal fees by year

  • 3rd year: $0
  • 4th year: $0
  • 5th year: $85
    • Total up to year 5: $85

Seek advice from a UK/EP patent attorney before filing solely in the UK, particularly for software inventions. Contact us directly for further information.

Notes

  • EP Renewal fees: €530 (3rd), €660 (4th), €925 (5th)
  • UK Renewal fees (upon grant): £70

Is your client concerned about the cost of filing an EP application, and is primarily interested in the UK market?

Consider filing in the UK directly in view of the much lower official fees [1] for a typical PCT national/regional phase entry in fall 2023:

  • EPO: c. $3,600 (if EPO was ISA) to $4,900 (if EPO was not ISA)
  • UKIPO: c. $350

Seek advice from a UK/EP patent attorney before filing solely in the UK, particularly for software inventions. Contact us directly for a breakdown of the above costs.

[1] UKIPO – Filing fee: £30 + Search fee: £150 + Exam fee: £100 = £280 ≈ $350

EPO was ISA – Filing fee: €135 + Exam fee: €2,055 + Designation fee: €660 + 3rd year renewal fee: €530 = €3,380 ≈ $3,600

EPO was not ISA – Filing fee: €135 + Search Fee: €1,460 + Exam fee: €1,840 + Designation fee: €660 + 3rd year renewal fee: €530 = €4,625 ≈ $4,900

Are you frustrated by the difference between unity requirements in the US and Europe?

The EPO considers claims to be unified when all claims recite at least one common feature which is novel and inventive.  Make sure your independent claims meet this requirement!

If in doubt, put the most commercially valuable claim first, as the EPO will use the search fee paid on filing to search this invention (and require additional search fees to search other inventions).

Regardless of whether additional search fees are paid, non-unified claims will have to be amended for unity or deleted, but divisional applications can be filed if desired.

Removal of the 10-day notification period

For many Communications issued before 1 November 2023, the time limit for responding was calculated from the 10th day after the date of the Communication to allow for postal delays.

The rule changed on 1 November 2023 so the time limit for responding is calculated directly from the date of the Communication – so no more ‘10 days’. The rule change only applies to Communications issued from 1 November 2023.

So, the first Rule 161/162 or Rule 70/70a Communications with the regular 6-month response term that this change will affect are coming up for response from 1 May 2024, so don’t forget that you no longer have the extra 10 days to provide your EP attorney with instructions!

The quirk of automatic validation for EP patents

Here’s a question we’re often asked : “My client only wanted to validate the European patent in the UK and Switzerland, so why does the EP register show it’s valid in Lichtenstein?”

Usually, after grant, the Applicant must choose in which EPC states to validate. This involves meeting the translation and fee requirements for each state.

However, some states have chosen to remove these validation requirements by signing the London Agreement, which aims to make the European patent regime lower cost and more attractive. In these states, validation is automatic and immediate upon grant.

The relevant states are: Belgium, France, Germany, Ireland, Luxembourg, Monaco, Switzerland, Liechtenstein and the United Kingdom.

However, whilst automatically validated in these states, the Applicant still retains control of whether to keep the patent alive in any particular state through selective payment or non-payment of the renewal fees. 

PACE - How to accelerate prosecution at the EPO

Is your client eager to speed up the prosecution of their patent application before the European patent office (EPO)?

Consider requesting accelerated search and/or examination of the application under the “Programme for Accelerated Prosecution of European Patent Applications” (also known as PACE).

  • What is the benefit of requesting PACE? – If requested during the search stage, the EPO will endeavour to issue the search report within six months from the PACE request. If requested during the exam stage, the EPO will endeavour to issue the first/next exam report within three months of the PACE request.
  • How can I request PACE – PACE can be requested once during the search stage, and/or once during the exam stage.
  • How much does PACE cost? PACE is a free service offered by the EPO.

To make use of PACE, the EPO expects applicants to reply to communications on time. This means that the EPO will remove an application from PACE if the applicant requests any extension of a time limit.

Notes

The EPO may not allow an applicant to request PACE for all their applications.

PACE requests are hidden from view of the public file.

EPO welcomes USPTO-like fee discount for micro-entities

Effective from 1 April 2024, the EPO is introducing a number of important fee changes.

Whilst these include the usual fee increases – this year by 4% – with the exception of filing, appeal and opposition fees, there’s also some good news that will be surprisingly familiar to our US colleagues…

…the introduction of a 30% reduction in all main fees for applicants deemed micro-entities.

The reduced fees include those for filing, examination, grant and renewal, and are available providing the applicant has filed fewer than 5 applications in the 5 years before the date of filing of the application concerned (or the date of EP regional phase entry for a PCT).

The micro-entity fee reductions are available for:

  • microenterprises
  • natural persons, and
  • non-profit organisations, universities or public research organisations

To benefit, applicants must declare which of the above applies, and this must be at the latest when making the first reduced fee payment.

For our US colleagues, it’s worth considering whether any of your clients qualifying for the USPTO micro-entity status may also qualify for the new EPO equivalent… especially for clients previously put off EP patents due to high fees!

Please get in touch if you’d like us to assess whether your client qualifies for these reduced fees, and for associated cost estimates.

Incorporation by reference – a pet peeve of the EPO.

Many US-originating patent applications include the expression “incorporated by reference” when there is a need to consider the content of another document when reading the patent application, without having to literally restate the content of the other document within the patent application.

While this approach is acceptable in the US, the EPO dislike “incorporated by reference” expressions and will require their deletion from the patent application.

Why? In Europe, a patent application must be self-contained, i.e. capable of being understood without reference to another document.

What does this deletion mean for the patent application?   This depends on whether the referenced document contains subject-matter that is “essential” for carrying out the invention.

Subject-matter is considered essential if it is needed for the application to disclose the invention sufficiently clearly and completely enough for the invention to be carried out by a skilled person.

If none of the content of the referenced document is essential, the deletion of “incorporated by reference” should not be problematic.

However, if any of the referenced subject-matter is essential, the essential subject-matter needs to be expressly incorporated into the patent application.

Doesn’t adding this essential subject-matter to the application lead to problems with added matter?

Not necessarily, if the subject-matter is taken word-for-word from the referenced document.  Note that there is very little scope for adapting the wording of the content of the referenced document to the particular features or terminology used in the patent application.

So, it is highly recommended that any essential subject matter is added to the patent application, and linked to the wording or terminology used in the patent application, before it is filed in Europe.

Can the content of a referenced document be used to support amendments to the claims of the patent application?

Only in very limited circumstances, and so, again, it is highly recommended that any essential subject matter is added to the patent application before it is filed in Europe.

Correcting an error before the EPO

What happens if a document filed at the European Patent Office (EPO) contains an error or a mistake?

Well, the rules of the European Patent Convention state that linguistic errors, errors of transcription, and mistakes in any document filed with the EPO may be corrected on request.

However, there is a specific caveat for corrections relating to the description, claims and drawings…

If a correction of an error concerns the description, claims or drawings, then the correction must be obvious in the sense that it is immediately evident that nothing else would have been intended than what is offered as the correction. This requirement can be tricky, as illustrated below:

2 + 2 = 3

Imagine the description includes the above equation. It’s obvious that an error exists here, and many may consider the correction to be obvious as well – but is this actually the case?

2 + 2 1 = 3

2 + 2 = 3 4

As shown above, there is more than one possible correction for the error, and it’s not immediately evident which one was originally intended.

As a result, there’s no guarantee that the error could be corrected before the EPO.

Of course, the previous examples have considered the error in isolation from the rest of the description, which may provide evidence that a particular correction is obvious.

Nevertheless, the example illustrates the bar that applicants must meet when attempting to correct an error in a patent application before the EPO.

Delay the filing of claims at the EPO with CAUTION...

Unlike US patent applications, European patent applications do not need to contain any claims in order to be given a filing date.

But be wary – late filing claims can be RISKY.

If an EP application does not contain any claims, the EPO will issue an invitation inviting the applicant to file one or more claims.

The invitation sets a 2 month deadline for the applicant to file their claims.

Delaying the filing of claims can be useful in many scenarios.

For example, an applicant may be eager to obtain a filing date (e.g. in anticipation of an upcoming public disclosure) but may be uncertain of the content and/or number of claims to file.

In such a scenario, the applicant could have originally agreed on a claim set containing 20 claims, but may be unsure whether to cut the number of claims to 15 – to avoid paying excess claims fees.

In such a case the claims could be included as numbered paragraphs in the description whilst the applicant decides which claims to pursue.

However, delaying the filing of claims can be risky.

The subject-matter of any such claims must be directly and unambiguously derivable from the EP application as originally filed – so as not to raise an added subject-matter objection.

Remember, added matter before the EPO is notoriously strict…

EPO Remedies – Further processing

What is further processing?

Further processing is the EPO’s standard remedy for failure to meet a deadline during prosecution of a patent application.

For example, if the deadline for responding to an exam report is missed, further processing can be used to effectively extend the deadline, for a price.

The application is deemed withdrawn and the EPO issues a loss of rights communication.

From the moment you miss the deadline, you’re in the further processing period. However, it is the loss of rights communication that sets the two-month deadline for requesting further processing and for responding to the exam report.

Since there is a delay between the application being considered withdrawn and the receipt of the loss of rights communication, the deadline for responding to the exam report is effectively extended by over two months. Hence your attorney won’t know the exact date of the extended deadline until the loss of rights communication is received.

What are the requirements for requesting further processing?

Within two months of the communication of loss of rights:

  • Pay the prescribed fee – the fee for further processing can vary depending on what is being remedied; and
  • Complete the omitted act(s) – e.g. respond to exam report

Note

  • Proceed with caution – not all deadlines and time limits can be remedied by further processing.
  • Further processing is available as of right – this means that the Applicant does not need to provide a reason for using further processing.

Limits on the number of independent claims in the US and Europe – what’s the difference?

There is a notable difference between US and European practice when considering how many independent claims to include in your patent application.

USPTO

The USPTO charges excess claims fees for any more than three independent claims. However, as long as the total number of claims is considered “reasonable” there’s no defined upper limit on the number of independent claims that can be included.

As such, a US patent application can include multiple independent claims in the same category (e.g. multiple independent product claims, and/or multiple independent process claims.

EPO

In contrast, the number of independent claims that can be included in a European patent application is limited to one per category (e.g. a single independent product claim, and/or a single independent process claim), with no option to pay for more.

However, there are three specific exceptions in which multiple independent claims in the same category is allowable.

EPO – exceptional circumstances

A European patent application may contain more than one independent claim in the same category only if the subject-matter of the application involves one of the following:

(a) a plurality of interrelated products, (b) different uses of a product or apparatus,

(c) alternative solutions to a particular problem, where it is inappropriate to cover these alternatives by a single claim.

EPO – examples of exceptional circumstances

(a) Interrelated products is usually interpreted to mean different objects that complement each other or work together – such as a plug and socket, or transmitter and receiver.

(b) Claims directed to further medical uses, when a first medical use is known, could be considered to fall under the exception of different uses of a product or apparatus.

(c) In some cases, a group of chemical compounds could reasonably be argued to involve alternative solutions to a particular problem.

In particular, whilst exceptions (b) and (c) seem generous, in practice they are much more limited!

Regardless, your EP attorney can help you review the claims to navigate these principles before EPO filing.

Europe’s inescapable trap – how to avoid getting caught!

The inescapable trap is a formidable by-product of two criteria laid out in the European Patent Convention (EPC) which dictate the way amendments can be made. The two criteria are as follows:

  1. A European patent application cannot be amended to extend its content beyond the application as filed (Article 123(2) EPC); and
  2. A European patent cannot be amended to extend its scope of protection (Article 123(3) EPC)

To explain how one can fall victim to the inescapable trap, consider a basic example.

Claim 1 of an application originally claims a laptop.

During prosecution, Claim 1 is amended to claim a laptop with circular keys.

The application is granted containing amended Claim 1.

The granted patent is opposed.

The opponent successfully argues that there is no basis in the application as filed for a laptop with circular keys.

Criterion A is not met and thus Claim 1 as granted is considered invalid.

To meet Criterion A, the proprietor may try to reverse the amendment such that Claim 1 claims a laptop only (i.e. as originally claimed).

However, such an amendment broadens the scope of protection and thus Criterion B is not met.

Result: The proprietor can neither remove the added-matter nor retain the added-matter.

The proprietor is now caught in the inescapable trap!

The possibility of the inescapable trap highlights the importance of  thoroughly and cautiously checking basis in the application as filed when amending the application.

However, there may be options for avoiding the inescapable trap in our example…

It may be the case that the application as filed only describes a laptop with circular keys in combination with a circular touchpad.

Therefore, Claim 1 could be amended to claim a laptop with circular keys and a circular touchpad.

In this way, the subject-matter of Claim 1 no longer extends beyond the content of the application as filed (satisfying Criterion A); and is a more limited version of Claim 1 as granted (satisfying Criterion B).

So here the proprietor has been able to avoid the inescapable trap, but only by limiting further.

Therefore, if you’re making an amendment during prosecution that may be considered to add matter, it’s useful to consider what basis there is for even further limiting amendments to reduce the claim scope, just in case this may be needed later… and if there’s no basis for further amendments, this could tip the scales on whether or not to risk that particular amendment!

EP novelty-only prior art v. US secret prior art

Assessing whether a patent application is novel and inventive/non-obvious requires determining what constitutes the prior art.

However, there’s an important distinction between US and European practice when it comes to the relevance of a particular type of prior art document – pre-filed, but post-published prior art.

To begin with, consider this scenario: Document D1 is not usually considered to be prior art for the patent application A1, since the date of D1’s disclosure occurs after the priority date of A1 (i.e. the “effective filing date” of A1). However, what happens when D1 is also a patent application?

In Europe, if A1 and D1 are both European patent applications, then D1 can be considered to be “novelty-only prior art” for A1, a.k.a. “Article 54(3) EPC prior art”. As such, D1 can be used in the assessment of novelty, but cannot be used to assess inventive step.

Further, even the patent applicant’s own prior applications are citeable against them in this manner.

In the US, the corresponding scenario is interpreted differently. If A1 and D1 are both US patent applications, then D1 is considered “secret prior art” for A1. But crucially, here D1 is used in the assessment of both novelty and obviousness.

However, in the US the applicant’s own prior applications cannot be cited against them as secret prior art.

Hence in summary:

  • Whilst the USPTO is able to rely on pre-filed, post-published prior art for the full assessment of both novelty and obviousness, the EPO can only rely on such prior art for the assessment of novelty.
  • Self-collision with your own unpublished applications is possible at the EPO, whereas your own secret applications at the USPTO are not citable in this manner.

As can be seen, understanding these distinctions between European and US practices is essential when developing a filing strategy involving both jurisdictions. 

Boosting your provisional patent application – why adding claim language is a smart idea

Since 1995, the USPTO has offered the option of filing a provisional application as an initial step for obtaining patent protection.

There are many advantages to filing such a provisional application.

A provisional application provides:

  • Simplified filing with a lower initial investment for the Applicant;
  • A 12 month period in which an invention’s commercial potential can be assessed before committing to a nonprovisional application; and
  • The all-important line in the sand – i.e. an official priority date.

A provisional application can provide an Applicant with a simplified filing process.

This simplicity is exemplified by the lack of requirement to include any claims in the provisional application.

However, this doesn’t mean that claim language should be ignored completely!

As suggested by the name, provisional applications are short-lived, and last for a non-extendible period of 12 months from filing. As such, if an Applicant wishes to pursue further protection, then a corresponding nonprovisional (“regular”) application has to be filed.

At this stage, having claim language in the provisional application can provide significant benefits to the Applicant.

Including claim language in a provisional application can:

  • Define the scope of invention – claim-like statements can help to outline the boundaries of the invention to be claimed;
  • Provide support for later applications – well-drafted claim-like statements can provide robust support for drafting the claims of nonprovisional applications. This is particularly useful in Europe, where added subject-matter requirements are strict; and
  • Prevent gaps in coverage – without taking the time to draft claim-like language, key aspects of the invention may be omitted from, or described unclearly in, the provisional application.

Of course, while there are strong benefits associated with including claim language in a provisional application, it is important to ensure that any such language is drafted in a broad and robust manner.

At HLK, we have built up considerable expertise in the field of provisional application drafting, so please get in touch to find out if a provisional application is the right choice for your patent strategy.

Third party observations before the EPO – are they right for you?

Did you know that third parties can submit observations on the patentability of an invention in a pending application at the EPO?

Third party observations (TPOs) can form a strategic and cost-effective tool for challenging the patentability of an invention before it is granted. As such, TPOs offer third parties a means to anonymously influence the outcome of a patent application without having to initiate formal opposition proceedings.

What type of observations can be submitted?

Comments on a lack of novelty and/or inventive step are the most common type of observation. However TPOs can be directed to a range of issues, such as clarity of claims, sufficiency of disclosure, and the allowability of certain amendments (e.g. added subject matter).

What are the requirements for submitting TPOs?

  • The relevant patent application must be published
  • The observations must be filed in English, French or German, and must include a statement of the grounds on which they are based (e.g. lack of novelty)
  • The party filing TPOs cannot be a “party to the proceedings” before the EPO
  • Proceedings in respect of the relevant patent application must be pending upon receipt of the TPOs

Is there a need for the third party to identify themselves?

No – TPOs can be submitted anonymously.

However, the third party does not become a party to the proceedings and thus is not informed of any action taken in response to the TPOs – so you do need to actively monitor the file. Nevertheless, the TPO, and the extent of the Examiner’s reliance on it, will be available for public inspection.

While TPOs provide a relatively low-cost mechanism for influencing the outcome of a patent application, navigating the nuances of the process before the EPO can be complex.

At HLK, we have built up considerable expertise in all manner of procedures before the EPO, so please get in touch if you are curious to discuss how TPOs could benefit your IP strategy.

Designs

Multiple designs: 1+1≠2

Applicants can benefit from significant cost savings in the UK and the EU by including two or more separate designs in a so-called multiple application.

In an EU design application, any number of designs may be included in a multiple application (from 2025 on there is a limit of 50 design), but they must all be within the same broad Locarno class (of which there are 32). (This requirement is expected to be removed in 2025).

In the UK, a multiple application can include a maximum of 50 designs, but there is no such requirement for the designs to be related in any way.

Once filed, each design undergoes a formalities examination, and once registered, each design is treated separately, with renewal fees falling due in respect of each.

Disclaimers

Both UK and EU design laws allow applicants to use disclaimers to control the scope of protection.

Both jurisdictions allow visual disclaimers to be included in the visual representations themselves, typically by using broken lines, shading or faded lines for those parts of the design that are not to be protected.

In the UK, written disclaimers may also be used, either on their own to exclude certain features, colour or texture from protection, or to clarify an accompanying visual disclaimer.

Scope defined (mainly) just by the drawings

In both UK and EU designs, the representations themselves define the scope of protection conferred. Unlike design patents in the US, there are no written claims defining what the applicant intends to protect.

An ‘Indication of Product’ must be included in each EU and UK design application, to indicate the product to which the design is intended to be applied or in which it is intended to be incorporated.

The Indication of Product does not limit the scope of protection conferred by the design.

In the EU, any description included in a design application does not have any legal effect on the scope of interpretation of the design. However, in the UK, a written disclaimer may be included which does have legal effect, so applicants should bear this in mind when including disclaimers.

Surface shading and contour lines

US design patent drawings require surface shading to indicate the character and contour of all surfaces. In contrast, such shading is not required in the EU and the UK and, in some cases, removal of such shading may be advisable.

On the one hand, to ensure any claim to priority is validly maintained, we recommend filing an EU or UK design application with drawings identical to those used in the priority application. On the other hand, however, there is a chance that a court in the UK or in a member state of the EU IPO could construe any such surface shading narrowly.

To give applicants the chance to maximise the scope of protection and to maximise the likelihood of a valid priority claim, a multiple application could be filed in the EU and/or the UK, including a set of drawings identical to those in the priority application, and a set of drawings with the surface shading removed.

Limit on the number of representations

We’re often asked how many representations or views of an article should be included in a design application.

The strict answer is “at least one”, but we typically include a top view, a bottom view, a left view, a right view, a front view and back view and a perspective view.

In the EU, a maximum of 7 views can be included in the design, with a further 3 “unprotected” views, for reference.

In the UK, a maximum of 12 views can be included, all of which define the protected design.

That said, in some cases, a single view can be sufficient, for example when illustrating a graphical user interface (GUI).

Graphical User Interfaces (GUIs)

The appearance of GUIs can be effectively protected using registered designs.

In a US design patent, a GUI is typically shown on a display of a device.

There is no requirement in the EU and the UK to show the display or the device on which the GUI is to be displayed.

Like in the US, the EU IPO and the UK IPO allow animated sequences of images or icons to be protected, meaning that dynamic GUIs can be protected as well as static images.

No prior art searching/substantive examination

Unlike in the US, no substantive examination is carried out in respect of EU and UK design applications. Each EU and UK design application is examined to ensure it meets certain formal requirements. In particular, the representations are examined to check they are in the proper format and relate to a single design only.

In general, once a design application meets the formal requirements, it will be registered. In the UK, this can typically be within two weeks, while in the EU, registration can take place within a day or two of filing a design application.

While this quick turnaround can be beneficial to applicants looking to get registered protection quickly, registered designs are published immediately, so applicants should exercise caution if early publication would be detrimental, for example if the drawings show details to be included in a future patent application. For such cases, deferment of publication of an EU or UK design is possible. 

Deferment of publication?

In some scenarios it may be important for an applicant to have design protection in place for a product, but without the design being made publicly available. In the US, this is typically not an issue since design patents are published only after they have been issued.

Due to the extremely quick registration process in the UK and the EU, however, publication of a design can be undesirable.

For example, if a design application includes images showing features of a product that are to form the basis of a patent application, it may be important for those images not to be published.

In such cases, deferment of publication can be requested in EU and UK design applications.

For EU designs, publication may be deferred for up to 30 months from the priority/filing date.

For UK designs, publication may be deferred for up to 12 months from the date of filing the application.

UPC

Cross-border injunctions UPC

The UPC offers a new model for patent enforcement by allowing a single court to grant injunctions effective across all UPC Member States. This reduces the historical need for patentees to run parallel infringement actions in multiple national courts, reducing costs, shortening timelines, and avoiding inconsistent results.

For Unitary Patents (UPs), any injunction issued by the UPC has the potential to cover all 18 Member States of the UPC. For classic European patents that have not been opted out, the UPC can also issue injunctions covering all UPC states where the patent is validated, offering similar benefits of consolidated enforcement.

UPC injunctions apply uniformly across the Member States, creating a level of territorial coherence that was previously unavailable in Europe.

The court also has the power to grant interim injunctions with the same territorial reach, provided the applicant demonstrates urgency, a likelihood of success on the merits, irreparable harm, and proportionality.

Enforcement is carried out nationally but triggered by the single UPC order. The order is executed using established national enforcement mechanisms, making the injunction territorially broad but procedurally grounded in national practice.

The UPC can also set periodic penalty payments for non-compliance. These accrue until the infringing acts stop and are enforceable through national procedures, giving the injunction coercive force across borders. Customs measures may also be used to prevent the circulation of infringing goods within the UPC territory.

What to do if you are served with an infringement action by the UPC

Being served with patent infringement proceedings by the UPC can be daunting for any business. Service of proceedings signals the start of a legal process that can have significant financial and operational consequences if not handled correctly.

Identifying when you’ve been served and understanding the immediate steps to take is crucial for protecting your rights and developing an effective response strategy.

In many cases, service will be by registered letter. If you are served in this way, you will receive a “Letter to Accompany Service”.

The key elements of the Letter to Accompany Service are as follows:

  • The date of issue of the Letter. This can be used to determine the date of deemed service, which is important for calculating deadlines for responding to the infringement claim.
  • An access code to allow your representative to access the case in the UPC’s case management system.
  • The number of the European patent that is alleged to be infringed.
  • The name of the defendant in the action (as specified by the claimant).
  • The name of the claimant in the action.
  • The identification number allocated to the infringement action by the UPC. This will need to be quoted in all pleadings and correspondence relating to the infringement action.
  • A warning that failure to respond may lead to a judgement in default against you.
  • The name of the UPC Division handling the infringement action. It may be possible to challenge the jurisdiction of the named Division in some circumstances.

The date of the Letter is the single most important piece of information in the letter, because it can be used to establish the date of service of the infringement claim, which in turn sets the deadline for filing a preliminary objection (one month from service) and the deadline for filing a defence and counterclaim for revocation of the patent (three months from service).

In general, service is deemed to have taken place on the tenth day following posting of the letter.

Note that the claimant will be informed of the date of deemed service of the infringement claim. This information is available to the defendant’s representative in the UPC’s case management system (CMS) but is not automatically communicated to the defendant.

You should therefore adopt a safety-first approach when calculating the deadlines that stem from the date of deemed service, using the earliest possible date of deemed service, which is the tenth day following the date of the Letter.

For example, if the Letter is dated 28 July 2025, it can be assumed that the deemed date of service will be 7 August 2025. The deadline for filing a preliminary objection can then be assumed to be 7 September 2025 and the deadline for filing a defence and counterclaim can be assumed to be 7 November 2025.

The access code is also critically important, as it allows your appointed representative to access the case in the UPC’s case management system and register themselves as the representative.

This will allow your representative to receive future correspondence from the UPC, and to lodge pleadings and other documents at the UPC.

The patent number identifies the European patent that is alleged to be infringed, and is of course necessary to evaluate the infringement claim and formulate a defence and counterclaim for revocation.

If you receive a Letter to Accompany Service from the UPC, the first thing you should do is forward it to your European Patent Attorney or UPC Representative. (Your European Patent Attorney may also be a UPC Representative, capable of dealing with a UPC infringement action.)

It is critical that you do this as soon as possible, as the deadlines for responding to an infringement action in the UPC are very short and are generally not extendable, while the amount of work required to prepare a comprehensive defence and counterclaim is significant. Forwarding the Letter to your European Patent Attorney or UPC Representative immediately will maximise the time available to formulate and implement an effective response strategy.

Note that if your business is based outside the contracting member states of the UPC (e.g. if your business is based in the US) but has a place of business (e.g. a branch office) in a UPC member state, you may be served at that place of business.

Similarly, if your business is based outside the UPC member states but has subsidiaries in UPC member states, it is likely that infringement proceedings will be brought against one or more of the subsidiaries in the UPC member states.

It is therefore important that you have processes in place to ensure that staff in branch offices or subsidiaries in UPC member states know:

  • How to identify the Letter to Accompany Service;
  • Where responsibility for dealing with the Letter lies within your business (e.g. with the Chief IP Counsel, Head of Legal or the like); and
  • To pass the Letter on to the responsible person as a matter of urgency.

Preliminary objections at the UPC

A preliminary objection is a way for the Defendant in an action before the Unified Patent Court (UPC) to challenge the UPC’s competence to hear the action.

The UPC’s jurisdiction can be challenged as a whole, e.g. because the European patent at issue has been opted out or an opt-out has not been validly withdrawn, or the competence of the particular UPC Division in which the action was brought can be challenged, e.g. because the defendant does not have a residence or place of business in the country that hosts that Division.

A preliminary objection cannot be used to challenge the substantive grounds for the action, e.g. to challenge an infringement claim or dispute the validity of a patent.

A decision on the preliminary objection may be made by the UPC before the merits of the dispute are considered, and in such cases a decision will be issued as quickly as possible.

However, the UPC is also permitted to defer deciding on a preliminary objection until the main proceedings.

A preliminary objection must be filed within one month of service of the statement of claim, and must include the grounds on which the preliminary objection is based and all the supporting facts and evidence.

If the defendant fails to lodge a preliminary objection within this period, they are considered to agree to the jurisdiction of the UPC for the dispute, and to the competence of the UPC Division chosen by the claimant.

Filing a preliminary objection rarely affects the deadline for filing a defence and counterclaim (three months from service of the statement of claim).

It is therefore important to begin preparing a defence and counterclaim in parallel with a preliminary objection, to ensure these submissions can be lodged in time if the preliminary objection is rejected or a decision on the preliminary objection is deferred.

If successful, a preliminary objection challenging the UPC’s jurisdiction can prevent unnecessary litigation in the UPC, saving the defendant the cost of defending the action (though there is always a risk that the claimant will bring an action in a national court if the UPC does not have jurisdiction).

If unsuccessful, the case proceeds on the merits. In such cases, the only effects of a preliminary objection may be to increase the cost of the litigation, and possibly to divert attention and resources away from the preparation of a comprehensive defence and counterclaim.

Therefore, defendants should consider the grounds for and likelihood of success of a preliminary objection at the earliest possible opportunity.

Unless a solid case can be made that the UPC lacks jurisdiction over the dispute, it may be that resources are better focused on addressing the substantive issues raised in the claim and preparing a comprehensive defence and counterclaim.

Defence and counterclaim at the UPC

When faced with a patent infringement action before the Unified Patent Court (UPC), the defence – and any counterclaim for revocation – are your primary tools for contesting the claim.

Preparing these submissions thoroughly is crucial, as the Rules of Procedure set strict requirements on timing, content, and admissibility of arguments and evidence.

Deadline for filing

The Statement of Defence (and any Counterclaim for Revocation) must be filed within three months of service of the Statement of Claim. Extensions are rarely granted, so early preparation is essential.

Statement of Defence

The Statement of Defence should be a comprehensive response to the infringement claim, and must include:

  • The legal reasons why the infringement action should fail, including any challenge to the claimant’s proposed claim construction;
  • The facts relied upon, including any challenges to facts asserted by the claimant;
  • The evidence relied on to support the facts, and an indication of any further evidence that will be submitted later; and
  • A list of documents (including witness statements) referred to in the Statement of Defence.

The importance of facts and evidence

The UPC is a front-loaded system that relies heavily on written arguments; cases are generally decided based on the materials submitted by the parties during the written procedure. Late-filed facts, arguments, or evidence may not be admitted unless they directly respond to new allegations raised later in the proceedings. Accordingly it is crucial that all arguments, facts and evidence that you may wish to rely on in your defence to the infringement claim are included in the Statement of Defence.

It is essential that every statement of fact in your pleadings is accompanied by an indication of the means of evidence (documents, expert opinions, witness statements, physical evidence, etc.) to prove it. Facts that are not substantiated by evidence will generally be less persuasive to the Court when it comes to deciding on the issue in question.

It is also essential that any alleged fact you dispute is explicitly denied and that the denial is substantiated with facts and evidence. Any fact that is not specifically contested will be deemed admitted.

Consequences of an incomplete defence

Failure to include comprehensive facts, arguments, and evidence at this stage may seriously prejudice your ability to defend the infringement claim or to challenge the validity of the patent. The UPC may disregard later submissions that could reasonably have been made in the initial defence and counterclaim.

Key takeaways

  • Act quickly: Begin preparing your defence as soon as you are served.
  • Be comprehensive: Address each allegation, provide facts and evidence, and deny any statement you disagree with.
  • Follow the Rules: The UPC applies strict procedural requirements – missing one can mean losing your chance to present key arguments.

Counterclaim for Revocation at the UPC

When faced with a patent infringement action before the Unified Patent Court (UPC), a Counterclaim for Revocation may be filed in addition to any defence of non-infringement.

Preparing these submissions thoroughly is crucial, as the Rules of Procedure set strict requirements on timing, content, and admissibility of arguments and evidence.

Deadline for filing

A Counterclaim for Revocation (and any Statement of Defence of non-infringement) must be filed within three months of service of the Statement of Claim. Extensions are rarely granted, so early preparation is is essential.

Counterclaim for revocation

The Counterclaim for Revocation should be a thorough submission on why the patent is invalid. It must include:

  • An indication whether revocation of the patent in its entirety, or of only some claims, is requested;
  • Legal reasons explaining why one or more grounds for revocation render the patent invalid, together with relevant arguments on claim construction;
  • The facts and evidence relied on, and an indication of any further evidence that will be submitted later;
  • A list of documents (including witness statements) referred to in the Counterclaim for Revocation.

Grounds for revocation

The Counterclaim for Revocation may be based on any of the following grounds:

  • The claimed invention is non-statutory subject-matter;
  • Lack of novelty;
  • Lack of inventive step;
  • Lack of enablement;
  • New matter (the content of the patent extends beyond the content of the application as filed);
  • Extension of the scope of protection (the claims have been broadened by a post-grant amendment);
  • Proprietor of the patent is not entitled to the patent (i.e. is not the inventor or successor in title to the inventor).

The importance of facts and evidence

The UPC is a front-loaded system that relies heavily on written arguments; cases are generally decided based on the materials submitted by the parties during the written procedure. Late-filed facts, arguments, or evidence are unlikely to be admitted. It is crucial that all arguments, facts and evidence that you wish to rely on to show invalidity are included in the Counterclaim for Revocation.

It is essential that every statement of fact in your pleadings is accompanied by an indication of the means of evidence (documents, expert opinions, witness statements, physical evidence, etc.) to prove it. Facts that are not substantiated by evidence will generally be less persuasive to the Court when it comes to deciding on the issue in question.

Consequences of an incomplete Counterclaim

Failure to include comprehensive facts, arguments, and evidence at this stage may seriously prejudice your ability to challenge the validity of the patent. The UPC may disregard later submissions that could reasonably have been made in the initial Counterclaim for Revocation.

Key Takeaways

  • Act quickly: Begin preparing invalidity arguments as soon as you are served.
  • Be comprehensive: Assert all relevant grounds for revocation and provide facts and evidence.
  • Follow the Rules: The UPC applies strict procedural requirements – missing one can mean losing your chance to present key arguments.

Security for costs at the UPC

What is security for costs?

A party to litigation can apply for security. This is where there are reasonable prospects of success and there is a risk that the other side will not be able to pay a cost award at the end of the proceedings due to their financial position, or because it may be difficult to enforce the cost award against them.

Security is particularly important for defendants who, unlike claimants, do not have a choice about becoming a party to proceedings and incur the costs involved.

What do the UPC rules say about security for costs?

The UPC’s Rules of Procedure (RoP) Rule 158 allow a party to request adequate security for legal costs and other expenses incurred by the other party.

So….either party to proceedings can request a decision on security from the Court, and a failure to comply with such an order may result in a decision by default being given by the Court.

But….a court may be reluctant to impose security on a defendant absent very compelling facts.

Key criteria / factors the court looks at

  • The requesting party must show legitimate and real concerns that a cost order might not be recoverable or its enforcement unduly burdensome.
  • The financial position of the claimant (or whichever party might be ordered to give security) is important.
  • It is not required that enforcement is impossible — it suffices that it would be “unduly burdensome” to enforce.
  • It is not required for the court to assess merits of the claim when deciding on security for costs.
  • Equity and access to justice concerns matter.

What has been developing at the UPC?

  • The court has set security of substantial numbers (€500,000+).
  • If circumstances change the court can amend or release a security order.
  • The fact that a claimant is a non practising entity (NPE) or licensing entity alone is not enough to justify security for costs.
  • If you are on the receiving end of an action, then you can request an order for security for costs from the claimant. Filing a counterclaim does not make you a claimant and so, the UPC will not order you to provide security for costs as counter-claimant.

Key takeaways

  • The UPC can order security for costs, primarily to protect a defendant from a claimant who may be unable to pay costs later.
  • Security against a defendant is possible under the rules but not yet been tested.
  • The claimant’s financial strength (assets, revenue, business model) is key.
  • The court must balance this with the claimant’s right to access justice.

Liability for costs and cost shifting

The general rule for liability for costs

A successful party shall be entitled to recover reasonable and proportionate legal costs and expenses from the unsuccessful party, subject to some exceptions.  This is known as the “costs shifting” rule.

Types of costs recoverable

Recoverable costs include:

  • court fees
  • costs of representation
  • witnesses
  • experts
  • interpreters and translators
  • “other expenses” not defined

The amount of costs recoverable is dependent on the value of the case before the court.

Exceptions to the costs shifting rule

There are exceptions which allow the court to disapply the usual costs shifting rule. These are:

  • Only “reasonable and proportionate” legal costs and other expenses may be recovered.
  • If the court considers it is not equitable for the general rule to apply, perhaps due to inequality in the power and financial status of the parties, it may disapply it.
  • If a party has caused the court or another party unnecessary costs, it must bear those costs regardless of whether it is successful.
  • If a party succeeds only in part or in exceptional circumstances, the court may order that costs be apportioned equitably or that the parties bear their own costs.

The costs “ceiling”

The amount of costs recoverable is subject to a “ceiling” which is determined by the value of the proceedings. The value of the proceedings will reflect “the objective interest pursued by the filing party at the time of filing the action”.

The costs ceilings scale is as follows:

Key criteria / factors the court looks at when considering the ceiling

In particularly complex cases or cases involving multiple languages, the court has discretion to raise the ceiling if a party requests. The court also has discretion to lower the ceiling of recoverable costs.

Some factors the court will consider when exercising such a discretion are:

  • Whether the amount of recoverable costs would threaten the economic viability of a party, especially if the party is an SME, university, non-profit organisation, public research organisation or natural person.
  • The procedural behaviour of the parties.
  • The applicable level of the ceiling for recoverable costs in comparison with the annual turnover of both parties.
  • The type of economic activity of both parties.
  • The impact of changing the ceiling on the other party.

Impact of abandonment

If the action is withdrawn, the party liable for the court fees will be reimbursed:

  • 60% if withdrawn before the closure of the written procedure
  • 40% if withdrawn before the closure of the interim procedure
  • 20% if withdrawn before the closure of the oral procedure

Impact of abandonment

If the action is concluded by settlement, the party liable for the court fees will be reimbursed:

  • 60% if settled before the closure of the written procedure
  • 40% if settled before the closure of the interim procedure
  • 20% if settled before the closure of the oral procedure

However, these reimbursements may be denied or decreased by the court in exceptional cases.

What has been developing at the UPC in this area?

  • Where a Claimant was ultimately successful in a revocation action through settlement, but the trigger for settlement was disclosure of prior art which could have been disclosed before filing the action, the claimant may be liable for the procedural costs of the defendants (Stäubli Tec-Systems GmbH v Konrad & Anor (UPC_CFI_372/2023).
  • A defendant who challenges allegations of infringement and validity after receiving a warning letter, but then gives a cease and desist undertaking shortly after being sued, is liable to pay the claimant’s costs as the claimant shall be regarded the winning party. The declaration itself implies that the claimant’s requests have been met (Meril GmbH and another v Edwards Lifesciences Corporation, UPC_CoA_2/2024).
  • If one party is partially unsuccessful, the costs do not always have to be apportioned proportionately. Where a party was only partially unsuccessful and the unsuccessful claim was relatively minor and did not cause further costs, its entire costs might still be awarded against the other party (Insulet Corporation v EOFlow Co Ltd UPC_CoA_768/2024 (ORD_69078/2024).

Key takeaways

The key takeaways are:

  • The general rule for costs liability at the UPC is the unsuccessful party pays for the successful party’s costs.
  • The value of the claim is key in determining the maximum costs recoverable – however the court can depart from this ceiling following a request and at its discretion.
  • A successful party is not always safe from costs liability as the court can depart from the general rule in exceptional circumstances or in the interests of equity.
  • Parties should be mindful to avoid incurring unnecessary costs, as it may be liable for these even if successful.

Key contacts

 

 

 

 

 

Olivia Crawford

Partner

UK & European Patent Attorney

 

 

 

 

 

 

Oliver Poskett

Senior Associate

UK & European Patent Attorney

 

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