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Changes to Occupational Safety Rules at the Beginning of the Year

Reading time: 7 minutes

As we reported in our extraordinary newsletter, Act XCIII of 1993 on Labour Safety (“Labour Safety and Health Act”) introduces new rules as of 1 January 2026 for employer organizations regarding the provision of conditions for occupational safety and health. In this article, we summarize the requirements necessary to comply with these obligations.

Principles and requirements

The Labour Safety and Health Act sets out in detail the requirements that employers must take into account to ensure occupational safety and health. In this context, employers must strive to avoid hazards, assess risks that cannot be avoided, and combat hazards at their source. Furthermore, undertakings are required to take human factors into consideration when designing workplaces and selecting work equipment and work processes, to apply the achievements of technical progress, to replace hazardous solutions with less hazardous ones, and to provide appropriate instructions to employees. Companies must develop a coherent and comprehensive prevention strategy covering work processes, technology, work organization, working conditions, social relationships, and the effects of workplace environmental factors.

The role of risk assessment

One of the employer’s most important obligations is the preparation and maintenance of a risk assessment, including risk management and the determination of preventive measures. The assessment is carried out by a specialist, who identifies the hazard sources, determines the group of employees exposed to risks, and assesses the nature of the hazards and the extent of exposure. The risk assessment must be carried out before the commencement of the activity and reviewed when justified—at least every five years. Justifiable cases include changes in technology, work equipment, the method of work, or the scope of the employer’s activities. A risk assessment is likewise justified and required if a work accident or occupational disease occurs in connection with deficiencies in the applied activity, technology, work equipment, or method of work. These tasks qualify in all cases as occupational safety and occupational health professional activities and may only be performed by persons with the prescribed qualifications.

Persons authorized to carry out risk assessments

The Labour Safety and Health Act also contains differentiated rules regarding the qualifications required to carry out risk assessments and to define the occupational safety and occupational health content of the prevention strategy, with particular regard to the hazard class and the number of employees. The detailed rules are set out in Decree 5/1993. (XII. 26.) MüM (hereinafter: “MüM Decree“), which classifies employers into hazard categories and stipulates the qualifications required to perform the tasks accordingly.

In the case of employers classified in hazard class III with a maximum of 50 employees (e.g., labour market service providers, IT infrastructure providers, and wholesale and retail trade in general), there has been no change since 1 July 2025, in accordance with the MÜM Decree, the activity may also be carried out by a person holding a specialist medical qualification in occupational medicine, industrial medicine, occupational hygiene, public health and epidemiology, preventive medicine and public health, or by a person holding a qualification as a public health or epidemiological inspector or supervisor.

As of 1 January 2026, a new rule provides that, for employers employing at least 50 employees, the occupational safety content of the prevention strategy must be developed by a person with higher-level occupational safety qualifications in the case of activities classified under Hazard Classes I and II pursuant to the MüM Decree, such as paper manufacturing, pharmaceutical manufacturing, machinery manufacturing, computer, electronic and optical product manufacturing, and tobacco product manufacturing.

Also introduced as of this year is the rule that, for activities classified under Hazard Class I pursuant to the MüM Decree—such as paper manufacturing, pharmaceutical manufacturing, and machinery manufacturing—the preparation of the risk assessment at employers employing at least 50 employees must be carried out by a person with higher-level occupational safety qualifications.

Special rules for teleworking

In the case of teleworking, the employee performs work for part or all of their working time at a location separate from the employer’s premises. In such cases, work may be performed using equipment provided by the employer or, by agreement, by the employee. Where equipment is provided by the employee, the employer must, as part of the risk assessment, ensure that the work equipment is in a safe condition that does not endanger health, while maintaining this condition is the employee’s responsibility.

If work is not performed using IT equipment, it may only be carried out at a remote workplace that has been preliminarily assessed by the employer as appropriate from an occupational safety perspective, and the employer must regularly monitor working conditions and compliance with the applicable rules.

The situation differs when work is performed using IT equipment. In such cases, the employer is not required to conduct a risk assessment; it is sufficient for the employer to inform the employee of the rules for ensuring safe and healthy working conditions and to oblige the employee to comply with these rules, and the employer may obtain a declaration from the employee acknowledging this obligation. The employer may keep a register of work equipment. The employee is required to select the place of remote work in compliance with these conditions. Compliance with the rules may, of course, be monitored remotely by the employer through the use of IT tools. Although an individual risk assessment is not required in this case, proper employee information and regular monitoring remain part of the employer’s occupational safety obligations.

Employer obligations and liability

The employer’s ongoing responsibility does not end with the preparation of documentation. Employers must ensure proper information and instruction for employees, regularly monitor working conditions and compliance with regulations, provide safe work equipment, and promptly investigate irregularities and reports. In addition, employers must ensure the proper usability and condition of personal protective equipment, as well as the lawful investigation of work accidents and occupational diseases.

Compliance with occupational safety regulations is also of outstanding importance from the perspective of employer liability for damages, as under Act I of 2012 on the Labour Code the employer bears objective liability for damage caused to employees in connection with the employment relationship. To be exempted from liability, the employer must prove that the damage was caused by a circumstance beyond its control that it could not have foreseen and that it was not reasonably expected to prevent or mitigate. Under this strict regulatory framework, any failure to comply with occupational safety regulations is necessarily assessed to the detriment of the employer. For these reasons, it is particularly important that employers always have up-to-date occupational safety measures in force and that these are properly and verifiably documented.

Summary

Occupational safety regulations make it clear that ensuring occupational safety and health is not merely a formal obligation, but one of the most important elements of employer responsibility. Failure to properly prepare and regularly review the risk assessment and prevention strategy, as well as failure to actually comply with occupational safety requirements, entails not only regulatory sanctions but also significant compensation risks, given the employer’s objective liability. Our firm is pleased to assist in preparing for regulatory changes and in establishing operations that comply with applicable legislation.

Photo source: pexels.com, suntorn somtong

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The foundations of artificial intelligence regulation in the European Union

Reading time: 4 minutes

In 2024, the European Union adopted its Artificial Intelligence Regulation (the “AI Regulation“), which established the world’s first comprehensive regulatory framework for artificial intelligence. The provisions of the AI Regulation will gradually become mandatory until August 2, 2027. The AI Regulation refers certain implementation and supervisory tasks to the Member States, as a result of which a domestic regulatory framework for the use of artificial intelligence (“AI“) was also promulgated in Hungary in the fall of 2025.

Given that the AI Regulation will have to be applied almost in its entirety from August this year, CLVPartners is launching a series of newsletters on artificial intelligence to help with preparations. The aim of the series of articles is to present the legal issues related to the use of artificial intelligence in a practical yet easy-to-understand way. In the first part of the series, we will outline the basic concept of the current EU and Hungarian regulatory framework and its main objectives.

Purpose of the AI Regulation, concept of its regulation

AI is one of the fastest-growing areas of technology, and according to some forecasts, its application could bring significant benefits across a wide range of economic and social activities. At the same time, the European Union has recognized that the use of AI also carries a number of risks, such as the risk that its inappropriate use could jeopardize the fundamental rights and freedoms protected by EU law.

The purpose of the AI Regulation is to ensure that the development and use of AI systems takes place within a responsible framework. It is important to note that the AI Regulation applies not only to manufacturers, importers, distributors, and service providers operating in the European Union, but also to companies outside the EU if their products or services are available on the EU market or have an impact on EU citizens. To this end, the AI Regulation imposes obligations on developers and users of AI systems and establishes a uniform regulatory system for their authorization on the EU market. The AI Regulation stipulates that its regulatory framework serves to strengthen transparency and accountability and to promote the spread of human-centered and reliable artificial intelligence. It also aims to eliminate discrimination and bias, while ensuring that EU fundamental values and rights are upheld and providing effective protection against the risks posed by AI systems.

The AI Regulation takes a risk-based approach, classifying AI systems into four risk categories and assigning different rules and obligations to each category. The use of so-called prohibited AI systems that pose an unacceptable risk, such as cognitive behavioral manipulation or emotion recognition in the workplace, is already prohibited in the European Union. High-risk AI systems are subject to strict requirements, in particular testing, transparency, and human oversight obligations, and may only be placed on the market once these requirements have been met. These include, among others, systems used in medical diagnostics, self-driving vehicles, or biometric identification. For low-risk AI systems, such as chatbots, transparency obligations are the main requirement, while the AI Regulation does not set out specific rules for minimal or risk-free AI systems.

The AI Regulation is directly applicable in all EU Member States and, due to its nature as a source of law, cannot be transposed into national law and does not need to be promulgated separately. As a result, the AI Regulation creates a uniform legal framework for the regulation of artificial intelligence throughout the European Union.

Hungarian regulations

In addition to creating a uniform EU regulatory framework, the AI Regulation also imposes several obligations on Member States. Accordingly, Member States, including Hungary, have begun to develop the institutional and legal frameworks necessary to ensure the effective implementation and supervision of the provisions of the AI Regulation.

Under the AI Regulation, the supervision of compliance with the requirements for AI systems classified in each risk category will be the responsibility of the Member States. Accordingly, Member States are required to designate a market surveillance authority and a notifying authority responsible for assessing technical compliance. In addition, each Member State must establish regulatory test environments to support the development of safe and lawful AI.

To ensure compliance with these requirements, in the fall of 2025, the Hungarian Parliament passed Act LXXV of 2025 on the implementation of the European Union’s Artificial Intelligence Regulation in Hungary (“AI Act“), which lays the foundations for the domestic regulatory and institutional structure. The AI Act is also implemented by Government Decree 344/2025 (X. 31.) on the implementation of Act LXXV of 2025 on the implementation of the European Union’s regulation on artificial intelligence in Hungary, which lays down detailed rules on the operation of authorities performing tasks related to artificial intelligence. (X. 31.) on the implementation of Act LXXV of 2025 on the implementation of the European Union’s regulation on artificial intelligence in Hungary (“AI Government Decree“), which lays down detailed rules on the functioning of authorities performing tasks related to artificial intelligence.

Under the AI Act, the reporting authority tasks are performed by a single body, the AI reporting authority. This authority is responsible for designating conformity assessment bodies that examine and certify the technical conformity of high-risk AI systems in advance. Under the provisions of the AI Government Decree, the National Accreditation Authority performs this task.

Under the AI Act, market surveillance tasks are also performed by a single authority. The market surveillance authority is responsible for examining the lawful use of AI systems after they have been placed on the market. The Act also requires the AI market surveillance authority to establish and operate an AI regulatory test environment from August 2026 and to act as a point of contact. Under the provisions of the AI Government Decree, the Minister for National Economy is responsible for performing these tasks.

The AI Act also establishes the Hungarian Artificial Intelligence Council, which acts as a coordinating and advisory body. The task of the Hungarian Artificial Intelligence Council is to promote the uniform interpretation of the AI Regulation in Hungary through guidelines and position statements.

Summary

In summary, it can be said that in 2024, the European Union was the first in the world to adopt a comprehensive regulatory framework whose primary objectives are to promote the spread of human-centered, transparent, and reliable artificial intelligence, protect EU fundamental values and rights, and adequately address the risks arising from AI systems. The AI Regulation applies a risk-based regulatory approach, setting differentiated requirements according to the risk posed by each AI system.

The AI Regulation is directly applicable in all Member States, but leaves the implementation and supervisory tasks to national authorities. As a result, in the fall of 2025, Hungary enacted the AI Act and the related AI Government Decree to ensure the domestic implementation of the AI Regulation.

Photo source: pexels.com, Dušan Cvetanović

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Amendment of the Civil Code – managing directors

Until now, the company and the managing director were jointly and severally liable towards third persons for non-contractual damages caused by the managing director in his executive capacity. Pursuant to the new provisions, only then will the managing director be jointly and severally liable with the company against third persons, if he has caused the damages wilfully in his capacity as managing director.

Furthermore, the amendment clarifies that the managing director’s liability for wilfully caused damage extends not only to non-contractual damages but also to contractual damages (until now contractual damages could only be claimed from the company, and not from the managing director).

 

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