The cybersecurity standard IEC 81001-5-1 focuses on how IT security needs to be taken into account in the software life cycle.
As a special standard for health software, it supplements IEC 82304-1 and IEC 62304 among others, and can close gaps that urgently need to be closed. The EU is currently planning to harmonize IEC 81001-5-1, with a current target date of May 24th, 2024.
In this article, you will find out:
IEC 81001-5-1 targets manufacturers of “Health Software”. This does not just include medical devices, it also includes other software used in the health sector.
Examples of health software that is not a medical device:
The standard therefore does not just target manufacturers of medical devices, but also manufacturers of software for the health sector, or “Health Software”.
“software intended to be used specifically for managing, maintaining, or improving health of individual persons, or the delivery of care, or which has been developed for the purpose of being incorporated into a medical device”
(Source: IEC 81001-5-1 3.15)
IEC 81001-5-1 also includes stakeholders other than manufacturers: the introduction highlights how important bilateral communication with other organization (such as healthcare delivery organizations) is. This exchange is specifically considered in the standard.
“This document applies to the development and maintenance of Health Software by a manufacturer, but recognizes the critical importance of bilateral communication with organizations (e.g. healthcare delivery organizations, HDOS) who have security responsibilities for the Health Software and the systems it is incorporated into, once the software has been developed and released.”
In this respect, IEC 81001-5-1 also deals with the relationship with Healthcare Delivery Organizations (HDOs), which share responsibility for cybersecurity with manufacturers. This aims to ensure, for example, that operators have enough information on the safe operation of the products from manufacturers.
For example, operators must inform manufacturers of problems with IT security promptly so they can work together to find solutions quickly.
“facility or enterprise such as a clinic or hospital that provides healthcare services”
(Source: ICE 81001-5-1, 3.16; identical in ISO 81001-1:2021, 3.1.4)
IEC 81001-5-1, entitled “Health software and health IT systems safety, effectiveness and security — Part 5-1: Security — Activities in the product life cycle” covers the entire life cycle of health software: from development through to post-marketing monitoring. In addition to the general information and specifications for the life cycle processes such as software development and software maintenance, the standard’s annexes also provide tips on best practice.
Many of the requirements in IEC 81001-5-1, though, are not new for manufacturers of medical devices and in some cases they are redundant: the standard takes content from numerous existing specifications such as the framework of the National Institute of Standards and Technology (NIST), guidance documents from the FDA and IEC 62443 (“Industrial communication networks - IT security for networks and systems”). Manufacturers who have taken into account the latest developments to date and complied with them will not be surprised
The requirements of IEC 81001-5-1, however, are noteworthy because, unlike comparable standards (such as IEC 62443), they are specifically tailored to the field of health software.
We have put together more information on the general requirements for IT security in the health care sector in a special article.
The general specifications of IEC 81001-5-1 for software relate to:
IEC 81001-5-1 contains specifications for the following processes:
These processes overlap with the processes in IEC 62304, but are specifically tailored to health software. More information on the relationship with IEC 62304 can be found below.
The annexes also offer a guide for how best to handle many relevant topics.
According to IEC 81001-5-1, manufacturers must implement a cybersecurity process into their quality management.
With regard to this, the standard states:
“The manufacturer” shall perform security activities in the product life cycle on the basis of an established and documented quality management system.”
IEC 81001-5-1 therefore leaves the question of whether cybersecurity is implemented as a separately described process or the corresponding activities are integrated into existing quality management system processes open.
“Upstream cybersecurity” (in other words IT security relating to collaboration with third parties) has proven to be very relevant in practice:
Suppliers can represent a security risk for health software. It is often small companies with limited knowledge of the field of software security that take insufficient security measures at a company level or during the development process.
Hackers are aware of this weakness. They focus on these gateways. Manufacturers should therefore carry out a critical evaluation of their suppliers as a matter of urgency.
Health software must be continuously improved. If manufacturers identify a cybersecurity problem on the market, they must provide a security update or patch if necessary,
but this is generally not sufficient. Manufacturers need to ask themselves the question of whether the cybersecurity problem occurred as a result of a cause in the quality management system as part of the continuous improvement process. Corresponding corrective actions must be implemented in their processes if necessary.
For example, network connection ports that were accidentally left open may have enabled an attack to be carried out. In this case, the manufacturer must ensure that the product is delivered with closed ports and they must provide for port scans in their product verification process.
The title of 5.7.5 of IEC 81001-5-1 is Managing conflicts of interest between testers and developers. It is about achieving objectivity when evaluating test results. The standard feels that the greatest possible objectivity is achieved through having testers and developers that are separate from one another. This can be achieved by having an internal testing team that is separate to the development team or by using external testing providers.
Although IEC 81001-5-1 does not bring with it any groundbreaking innovations, it does specify the regulations of other standards more precisely for health software.
Health software may differ from other medical devices or software in terms of
- the role of the operator (healthcare delivery organization),
- the link to risk management according to ISO 14971 in the field of safety, and
- the reference to other standards from the health environment.
To date, only IEC 82304-1 and ISO 82304-2 were specifically for health software. IEC 82304-1, though, only sets out general requirements of the software life cycle (IEC 82304-1: “General requirements for product safety”. It primarily focuses on dangers that may be caused by the product itself (such as danger to humans caused by defective software).
In contrast to this, IEC 81001-5-1 requires a development process according to ISO 62304 and ISO 82304 and states which specific activities are necessary in the respective phases of the development process to ensure cybersecurity. In this respect, 81001-5-1 functions as a supplement to IEC 82304-1 and IEC 62304.
ISO 82304-2 differs in terms of the scope and the objective, as ISO 82304-2 relates specifically to quality labels for health apps.
IEC 81001-5-1 also closes the gaps in specific standards for medical device manufacturers who provide software within the scope of the MDR. While all other topics from Annex I MDR area already broadly covered by standards that are harmonized (or yet to be harmonized), this is missing for the field of IT security (Annex I point 17.2 MDR).
In addition to the MDR, to date there was only the Guideline MDCG 2019-16 (Guidance on Cybersecurity for medical devices). This summarizes the requirements of the MDR in terms of cybersecurity and provides reflections and background. IEC 81001-5-1, meanwhile, contains specific and compact requirements for manufacturers.
Otherwise, to date manufacturers have had to rely on guides such as that of the Johner Institute or the standard IEC 62443-4-1, which is from outside the industry. IEC 62443-4-1, for example, does not just take into account the special features of medical devices.
The overlaps with the related (but not specific to medical devices) standards IEC 62443-4-1 and IEC 62304 were taken into account in the draft of IEC 81001-5-1. The relationship with both standards is explicitly explained in Annex A of IEC 81001-5-1.
Since IEC 81001-5-1 covers important points under EU law about which there has as yet not been a standard, it is already on the EU’s application list for harmonization (heading “Attachment”, pos. 27) before it is even published. The implementation is planned for May 24th, 2024.
IEC 81001-5-1 addresses numerous point that have already been discussed in other documents, e.g. in the guideline of the Johner Institute on cybersecurity (IT Security Guideline), but the new IEC standard remains abstract in many places.
One example of this is the “Intended product security context”. Here, the standard merely states that this must be documented. It would be more helpful to describe the practical implementation in detail, which could look something like this:
“- the manufacturer has identified all neighboring systems (e.g. medical devices, IT systems, cloud services) that may be connected to the product."
"- the manufacturer has created a list of roles (people, neighboring systems) that may interact with the product.”
(Source: IT Security Guideline of the Johner Institute)
In this respect, IEC 81001-5-1 is helping to implement the procedural landscape. More specific details in some places would help manufacturers to meet the requirements. Other documents such as the IT Security Guideline should therefore continue to be used as checklists.
All in all, IEC 81001-5-1 is a very important standard that was long overdue. Uniform standards for cybersecurity in the field of medical devices have been needed for a long time. That was why the Johner Institute provided an IT Security Guideline some time ago. It provides important additions to existing standards and the new IEC 81001-5-1.
The fact that the standard had been intended for harmonization with EU regulations even before it was published also shows how much a standard of this type was needed.
IEC 81001-5-1 will also help the notified bodies. They will be able to use the standard as the basis for audits of the quality management system and the technical documentation in the future.
Manufacturers of medical devices should implement IEC 81001-5-1 as soon as it is published. It will already be significant as the “state of the art” even before the official harmonization.
You can use the IT Security Guideline by the Johner Institute as a guide when looking at the security of your health software. You can contact us at any time if you have any questions about the topic. You can use this form or simply send an email.