As of 26 May, new rules on in vitro diagnostic medical devices (IVDR) such as HIV tests, pregnancy tests or COVID-19 tests, are applicable.
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1. What are in vitro diagnostic medical devices?
In vitro diagnostic medical devices are tests used on biological samples to determine the status of a person’s health. There is a broad range of in vitro diagnostics (IVDs), from self-tests for pregnancy and blood glucose tests for diabetics, to sophisticated tests performed in clinical laboratories, for example to screen blood donations for various infections or to match up the donor and recipient for a transfusion. SARS-CoV-2 tests are also IVDs.
2. Why are new rules on in vitro medical devices needed?
The first EU-level rules for placing IVDs on the market were created in 1998. To reflect the substantial technological and scientific progress in this sector over the last 20 years, the EU lawmakers updated the rules to improve the safety of medical devices, modernise the sector and consolidate the EU’s role as a global leader in this area.
The Regulation on in vitro diagnostic medical devices (IVD Regulation) entered into force in May 2017 and becomes applicable on 26 May 2022. The IVD Regulation seeks to ensure a high level of public health and patient safety, taking into account scientific progress, as well as a smooth operation of the single market for these products. It was adopted together with the Regulation on medical devices that is applicable since 26 May 2021.
3. What are the main benefits of the new regulation?
The new rules on in vitro medical devices contain a number of improvements, including:
- clear obligations for economic operators (manufacturers, importers, distributors);
- introduction of a risk-based classification system with 4 risk classes of IVDs: class A (low individual risk and low public health risk), class B (moderate individual risk and/or low public health risk), class C (high individual risk and/or moderate public health risk) and class D (high individual risk and high public health risk);
- stricter control for high-risk in vitro diagnostic devicesvia a new pre-market scrutiny mechanism with a pool of experts at EU level;
- reinforcement of the criteria for the designation and oversight of notified bodies (a ‘notified body’ is an independent third party conformity assessment body) more information below;
- improved transparencythrough a comprehensive EU database on medical devices (Eudamed), parts of which will be publicly accessible more information below;
- a traceability system based on a unique device identifier (UDI);
- reinforced rules on clinical evidence and performance evaluation, including an EU-wide coordinated procedure for authorising multi-centre performance studies;
- strengthened post-market surveillancerequirements for manufacturers;
- improved coordination mechanisms between EU countries on vigilance and market surveillance;
- a specific regime for devices manufactured and used in the same health institution (‘in-house devices’).
4. What does the application of the Regulation mean in practice?
New devices being placed on the EU market from 26 May 2022, regardless of their risk class, must follow the rules of the Regulation. Existing devices for which the manufacturer significantly changes either the intended purpose or the design must also follow the Regulation, as opposed to the old Directive.
All class A non-sterile devices (such as laboratory instruments), regardless whether new or already on the market, must comply with the Regulation from 26 May 2022.
According to the Regulation’s transitional provisions, existing devices other than class A non-sterile that comply with Directive 98/79/EC may still be placed on the market during transitional periods under certain conditions. Several requirements of the Regulation already apply also to those devices, such as the registration of devices and economic operators, market surveillance and vigilance.
5. Why were the transitional provisions of the IVD Regulation amended?
Due to resources being diverted to addressing the COVID-19 pandemic and the substantial changes introduced by the IVD Regulation, Member States’ authorities, health institutions, notified bodies and economic operators were not ready to fully meet the requirements of the IVD Regulation at the date of application on 26 May 2022.
In particular, with only seven notified bodies designated so far under the IVD Regulation, there is a grave shortage of notified body capacity, making it difficult for manufacturers to conduct the legally required conformity assessment procedures in time. As the currently designated notified bodies are established in only four countries (Germany, France, the Netherlands and Slovakia), the situation is particularly problematic for SMEs established in other Member States, which have a tendency to apply to notified bodies in their own or neighbouring Member States.
If not addressed, this situation would have led to a significant disruption in the supply of a multitude of in vitro diagnostic medical devices on the market both for health institutions and for the public. This is why the European Parliament and Council adopted Regulation (EU) 2022/112, on the basis of a proposal from the European Commission.
6. Which transitional periods will apply?
For in vitro diagnostic medical devices with a certificate issued by a notified body in accordance with the previous Directive before 26 May 2022, there is now a transitional period until May 2025. However, only devices that require a notified body certificate already under the previous Directive (around 8%) will benefit from this existing transitional provision.
In order to address the shortage of notified body capacity more broadly, additional transitional periods were introduced for IVDs that have to undergo a conformity assessment involving notified bodies for the first time under the IVD Regulation.
The transitional provisions differentiate between risk classes:
- for high risk devices (class D) there is a transition period until May 2025,
- for class C devices the transition period lasts until May 2026
- for lower risk devices (class B and A sterile) it lasts until May 2027.
Devices that are concerned by the additional transitional periods may make use of them only provided they satisfy certain conditions, notably they continue to comply with the Directive and there are no significant changes in their design and intended purpose. This approach aims to balance the available notified body capacity with a high level of public health protection.
As mentioned above, there is no transitional period for the lowest-risk devices, class A non-sterile.
7. What is the role of notified bodies?
Unlike medicinal products, medical devices, including in vitro diagnostic medical devices, are not subject to a pre-market authorisation by a regulatory authority. Instead, medium and high risk devices are subject to a conformity assessment procedure involving an independent third party known as a ‘notified body’.
Notified bodies are designated and monitored by the Member States and act under the control of the national authorities. Since 2013, assessments of notified bodies are performed by a joint team of members from other Member States and the Commission. Under the new framework, the successful experience of these joint assessments for the designation of notified bodies is reinforced.
Under the previous Directive on in vitro diagnostics, only a relatively small number of high-risk in vitro diagnostic medical devices is subject to notified body control (about 8% of all in vitro diagnostics on the market). Under the IVD Regulation, around 80% of in vitro diagnostic medical devices will be under the control of notified bodies, the vast majority of them for the first time (MedTech Europe Survey Report, 8 September 2021, page 4).
Under the new IVD Regulation, the notified bodies must also consult an independent panel of experts on certain high-risk devices before the final decision on the certification of the product is taken. This will help a notified body to make more informed decisions, drive innovation while preserving a high level of safety and performance of products.
8. Why are there so few notified bodies?
Notified bodies are in most cases private for-profit entities. Their establishment is therefore market-driven. Under the current Directive 98/79/EC on in vitro diagnostic medical devices, 18 notified bodies are designated (22 before the UK’s withdrawal from the EU). So far, only 7 notified bodies have been designated under the IVD Regulation. 11 applications for designation are pending (May 2022).
The IVD Regulation, like the Regulation on medical devices, has reinforced the criteria for the designation and oversight of notified bodies. While this is necessary for a high level of safety and performance of devices, it also makes it more challenging for a candidate notified body to apply. Moreover, it may be a challenge to identify and recruit personnel with specific qualifications required for notified body staff in the in vitro diagnostics sector.
Together with Member States’ authorities and relevant stakeholders, the Commission is closely monitoring the situation on the market, including notified body capacity and preparedness of manufacturers to submit applications for certification, and is considering measures to address the shortage of notified body capacity.
9. Besides notified bodies, is the other necessary infrastructure in place to ensure application of the Regulation from May 2022?
Besides limited notified body capacity, all the other legal prerequisites for placing devices on the market are in place. The expert panels are the only legally obligatory component of the conformity assessment system of the highest risk (class D) IVDs in addition to the notified bodies. They are already operating, have started receiving submissions and issued scientific opinions.
The IVD Regulation provides the possibility for other optional elements, for example to designate EU reference laboratories and to adopt common specifications. However, neither the EU reference laboratories nor common specifications for IVDs are a pre-condition for the application of the IVD Regulation. It is possible to place devices on the market without them, after the assessment by the notified body and in some cases an expert panel.
For some less common class D devices it could be the case that there will be no EU reference laboratory as there may be no candidate laboratories. It may also be that there is insufficient scientific consensus in the field to produce common specifications for those less common class D devices. Such devices can nevertheless be legally placed on the market and made available to patients.
Even though they are not obligatory, it would be very helpful for the sector to have EU reference laboratories designated and common specifications available. The Commission is working on establishing the EU reference laboratories and adopting common specifications for 16 types of IVDs.
10. What is the state of play of the medical devices database Eudamed?
Eudamed will provide an overview of all medical devices available in the European Union. It will be composed of six modules related to: actor registration, unique device identification (UDI) and device registration, notified bodies and certificates, clinical investigations and performance studies, vigilance and market surveillance. It will integrate different electronic systems with information about medical devices and related companies (e.g. manufacturers).
The development of Eudamed is progressing, with the first Eudamed module on actor registration made available in December 2020. Since the beginning of October 2021, the second and third modules are available, namely the module on UDI/device registration and the module on certificates and notified bodies, except for the mechanism for scrutiny and the clinical evaluation consultation procedure functionalities (CECP) (the latter relevant only to medical devices such as implants and not in vitro diagnostics). The remaining modules as well as the functionalities for the mechanism for scrutiny and the CECP will be released when Eudamed is fully functional.
The Commission will continue to work in close cooperation with the Member States on this highly complex project.
11. What are the rules for ‘in-house devices’?
‘In-house devices’, also referred to as ‘laboratory-developed tests’ are manufactured and used within the same health institution. They are not marketed or transferred to other legal entities and do not bear the CE marking. In-house devices developed in laboratories can be essential for the diagnosis and treatment, especially for rare diseases.
With the exception of the general safety and performance requirements laid down in Annex I of the IVD Regulation, in-house devices are exempted from the IVD Regulation requirements, provided the health institution meets a number of conditions set out in Article 5(5) of the Regulation.
Among other things, health institutions must have an appropriate quality management system, comply with the international standard setting out the quality and competence requirements for medical laboratories (EN ISO 15189) or other national provisions, and must justify that the target patient group’s specific needs cannot appropriately be met by an equivalent in vitro diagnostic medical device available on the market.
Since the outbreak of the pandemic, many health institutions, in particular hospitals, have had to focus their efforts on dealing with COVID-19. Therefore Regulation (EU) 2022/112 postpones the application of most of the conditions to be met by health institutions making in-house devices by 2 years until 26 May 2024. The requirement for the justification that there is no equivalent CE marked device available to meet the target patient group’s specific needs is postponed even further, until 26 May 2028, as the health institutions will need an overview of CE-marked in vitro diagnostic medical devices available on the market to comply with this requirement.
Medical Devices – New regulations
Source: European Commission
