Standard essential patents: What the medtech industry needs to know

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Howard Wright, a partner and patent attorney at European intellectual property firm, Withers & Rogers, explains what medtech firms need to know about standard essential patents.

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The rapid growth of the medtech sector as it aims to equip people to monitor and manage their own health conditions at home means that more innovators in the sector may be coming into contact with standard essential patents (SEPs) for the first time. Is this a risk or an opportunity, and what exactly do they need to know?

SEPs are familiar to innovative companies in the consumer electronics sector, especially in relation to mobile phone technology. SEPs are patents covering inventions which form part of a standard. Standards, such as 4G or 5G, aim to provide a standardised approach to technology, and are important for ensuring technological interoperability between devices and methods offered by different manufacturers and innovators. By law, SEP holders must be willing to offer a licence to implementers to use their SEP technology. By doing so, they will facilitate the sharing of patented technologies that are required for a product to meet a mandatory industry standard.

Without access to telecommunication standards, it would be virtually impossible for smartphone owners to communicate with other smartphone owners, regardless of which phone network or operating system they are using, wherever they are in the world. The law aims to ensure that SEP holders cannot prevent their competitors from operating according to a standard, without the competitor first being offered the opportunity to take a licence.

Whilst able to realise value from their innovations by licensing them to third parties, SEP holders must be willing to do so on fair, reasonable and non-discriminatory (FRAND) terms. If a SEP holder fails or refuses to offer to license its intellectual property rights (IPR) to a prospective licensee on FRAND terms, it could be in breach of antitrust regulations in the UK, EU, and many other global jurisdictions.

In the medtech sector, the rapid rise in innovation activity aimed at monitoring, analysing, and transferring patient data is leading to the development of technologies that require the use of smartphones and phone networks. As such, more innovators in the sector may be finding it necessary to interface with SEP owners in the telecoms sector for the first time. There is also a possibility that as this sphere of technological innovation expands, there could be a need for new standards in the future, particularly as new medtech devices are generating large amounts of data on patients that must be collected, transmitted, and analysed. It will be beneficial to both patients and medical practitioners to do this in a standardised way, to provide greater understanding of the outcomes of medical interventions, which can then feed into the development of future medical treatment preventative measures.

In the UK, the Government published a call for views to find out whether SEPs are functioning efficiently and effectively and whether SEP holders are adhering to FRAND terms. The findings show that whilst most respondents believe SEPs help to create a balanced ecosystem, some felt that there was still some imbalance, with one side benefitting more than the other. For example, there was concern that SEP holders could leverage their market power and the threat of court action to dictate excessive royalty rates. Based on these findings, it is possible that standards might tighten in the future, although it seems unlikely that the UK Government would take this action unilaterally.

Due to the largely discretionary nature of the guidance and rules relating to the use SEPs, there have been some high-profile legal disputes. Most have centred on what it means for holders to be fair, reasonable, and non-discriminatory and what enforcement rights they should have access to. For example, after considering questions raised by Unwired Planet v Huawei, the Supreme Court confirmed that a UK Court has the power to grant an injunction to prevent a SEP’s infringement and to determine the terms of a global FRAND licence agreement. Increased use of SEPs by medtech innovators could mean that more disputes are likely in the future.

The principles behind the use of SEPs are not totally new in healthcare. During the COVID-19 pandemic, innovators involved in the development of vaccines faced pressure to waive IP rights to make patented technologies available to as many people as possible, as quickly as possible. The World Health Organisation established a COVID-19 Technology Access Pool to hold patented technologies that might need to be shared quickly under licence across the global biotech and pharmaceutical industry. While patent pools are not the same as SEPs, they are rooted in the same principles, encouraging the sharing of technologies on fair and reasonable terms. A patent pool enables a third party to seek licences to multiple patents, often from multiple patent holders, in a single transaction, consequently, improving and simplifying access to the patented technologies. Patent pools may become particularly useful as medtech innovators increasingly seek to incorporate new technologies, such as communication functions, into their products and services.

For innovators working in the fields of telemetry and biometric analysis and diagnostics, it is especially important to be aware of SEPs and how to use them. Here’s some key advice to bear in mind:

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