Health Care

Explore three essential health care standards—SIST EN 17984-6:2025, SIST EN 4641-102:2025, and SIST IEC 60050-826:2023—that address medical equipment accessibility, quality assurance, and terminology for electrical installations. This comprehensive article demystifies compliance for organizations including hospitals, care facilities, medical device manufacturers, aerospace suppliers, and public service providers. Understand requirements for assistance dog accessibility, robust optical cables for critical environments, and coherent vocabulary for safe electrical installations. Perfect for professionals aiming to scale operations, enhance compliance, and deliver inclusive, safe, and reliable health care services. Discover actionable insights, practical implementation tips, and direct links to the official standards on iTeh Standards.

Explore the latest advancements in health care technology with the publication of two essential standards for ophthalmic optics in January 2026. This article covers ISO 11986:2026 and ISO 11987:2026, addressing preservative uptake/release in contact lenses and reliable shelf-life determination. Discover critical updates impacting manufacturers and organizations in the eye care sector, including best practices for compliance and implementation. Stay ahead in ensuring the safety, efficacy, and quality of contact lenses and care products by understanding how these new standards affect innovation, regulatory demands, and day-to-day industry operations. Essential reading for professionals focused on quality, compliance, or product development in the health care technology sector.

Explore the latest updates in health care technology standards released in January 2026. This comprehensive review covers five critical new and revised standards in areas such as medical electrical equipment, wheelchair seating, external cardiac pacemakers, and animal health diagnostics. Gain insight into new safety and performance requirements, test protocols, regulatory compliance, and harmonization best practices in medical device manufacturing and diagnostics. Essential reading for quality managers, compliance officers, engineers, procurement specialists, and health technology professionals seeking to ensure conformity, optimize safety, and stay ahead in the rapidly evolving health care sector.

Explore the latest international standards published in January 2026 for the health care technology sector. This comprehensive article covers five crucial standards, including new requirements for medical electrical equipment, hospital beds for children, washer-disinfectors for non-critical devices, and key guidelines in traditional Chinese medicine. Professionals in health care, compliance, quality management, engineering, procurement, and research will find essential updates on safety, performance, and implementation. Discover the impact these standards will have on clinical practice, patient safety, operational processes, and global trade, and learn what steps your organization should take to ensure timely compliance and ongoing excellence.

Discover the critical January 2026 update in healthcare technology standards with the newly published prEN IEC 80601-2-23:2024. This international standard focuses on the safety and essential performance of transcutaneous partial pressure monitoring equipment, ensuring reliable patient monitoring and enhanced compliance for medical device manufacturers and clinical facilities. Explore comprehensive details on requirements, industry impact, and technical implementation, with direct access to the full standard. Stay informed about how these updates will influence diagnostic equipment safety, quality assurance, and regulatory compliance for healthcare professionals.

Explore December 2025’s key international standards updates for health care technology, covering sleep apnoea therapy masks, diagnostic X-ray equipment, and the safety of radiotherapy treatment planning software. This in-depth review (Part 2 of 3) highlights five standards essential for manufacturers, clinicians, compliance officers, and technology providers. Learn about new safety requirements, revised test protocols for medical imaging equipment, adaptive radiotherapy requirements, and harmonized global guidelines. Discover the benefits of timely adoption, compliance implications, and industry best practices, with authoritative links to the full standards on iTeh Standards. Stay ahead of regulatory requirements—read on for actionable insights and practical impact analysis.

Explore the latest December 2025 health care technology standards critical to patient safety and device performance. This article reviews five new international specifications for pediatric medical beds and sleep apnoea breathing therapy equipment, with a focus on IEC 80601-2-89:2025 and EN ISO 80601-2-70:2025. Professionals and compliance specialists will gain actionable insights into requirements for mechanical safety, electrical integrity, patient entrapment protection, and breakthrough changes tailored for children and home care users. Discover who must comply, how implementation impacts hospital workflows and procurement, and the advantages of early adoption. Stay up to date with authoritative industry guidelines and direct links to official standards on iTeh Standards.

Explore the latest updates in health care technology standards for December 2025. This in-depth feature covers five newly published international standards, including advances in the biological evaluation of medical devices, updated requirements for transfusion equipment, performance tests for radionuclide imaging devices, and quality guidelines for traditional Chinese medicine (Gastrodia elata tuber). Learn about key changes, compliance expectations, and best practices for implementation, specially tailored for industry professionals and leaders. Stay ahead of regulatory shifts and quality expectations in the evolving landscape of health care technology with expert insights and direct access to the full standards on iTeh Standards.

Discover the December 2025 release of EN 17984-3:2025, a groundbreaking European standard setting out core and specialist competencies for professionals working with assistance dogs. This comprehensive guideline, essential for health care organizations and assistance dog providers, improves quality, consistency, and safety across roles such as breeding, training, assessment, and instruction. Learn what’s new, who must comply, and how this benefits organizations, professionals, and stakeholders in health care technology. Stay ahead on compliance and best practices by exploring the detailed insights and practical steps presented in this authoritative iTeh Standards news article.

Discover the November 2025 updates in health care technology standards with this detailed review covering five newly published international specifications. This comprehensive article is essential reading for medical technology professionals, compliance officers, procurement specialists, and quality managers. We explore updates to standards on tissue-engineered products, hip joint prosthesis testing, sleep apnoea breathing therapy equipment (with parallel ISO and IEC releases), and advanced airborne room disinfection processes. Learn about scope, technical requirements, implementation implications, and how these standards shape safety, quality control, and regulatory compliance. Stay ahead in the health care sector by understanding how these vital standards impact your operations and why proactive adoption is a key to maintaining excellence.

Explore the latest developments in health care technology standards with our November 2025 update. This comprehensive article covers three newly published international standards focusing on dental product safety and animal welfare in medical device testing. Professionals in dentistry, medical manufacturing, quality management, and regulatory compliance will find key insights on ISO 11040-3:2025 (dental syringe cartridge seals), ISO 6876:2025 (endodontic sealing materials), and prEN ISO 10993-2 (animal welfare for device biocompatibility testing). Learn about new requirements, major changes, compliance considerations, and best practices for effective implementation. Stay current and ensure your organization meets international benchmarks in safety, quality, and ethical research by reviewing these critical updates.

Stay ahead in the evolving world of health care technology with this comprehensive overview of five newly published international standards in November 2025. This article, part 3 of 4, covers critical updates including biological evaluation of medical devices, small-bore connector requirements for liquid and gas applications, safety of transportable liquid oxygen systems, system reliability for single-use drug delivery systems, and dental endodontic sealing materials. Learn about the latest compliance requirements, technical specifications, and best practices impacting industry professionals, quality managers, engineers, and procurement specialists. Dive in to discover key highlights, actionable insights, and how these updated standards will drive higher safety, efficacy, and operational efficiency across medical and dental technologies.

Explore the first part of our November 2025 coverage on newly published international standards in health care technology. This article details five significant standards, including essential updates for medical device marking in MR environments, liquid oxygen systems for home care, sleep apnoea therapy accessories, and testing implants for spinal disc prostheses. Gain insight into technical requirements, compliance implications, and industry best practices, with practical guidance for quality managers, compliance officers, engineers, and procurement specialists overseeing medical devices and technologies. Stay informed with authoritative backlinks to the full standards on iTeh Standards.

This monthly overview examines the standards published in October 2025 for the Health Care sector. In Part 2, we review five key standards that address medical supply units, traditional Chinese medicines, dental elevators, textile disinfection, and medicinal root quality. These publications highlight ongoing priorities in patient safety, device performance, infection control, and the growing global regulation of natural medicines. Industry professionals, quality managers, and compliance officers will benefit from concise summaries, analysis of emerging themes, and practical recommendations for compliance. Discover what these standards mean for the future of Health Care and stay informed on recent regulatory directions.

This monthly overview examines five significant standards published in October 2025 for the Health Care Technology sector. Covering critical updates to small-bore medical connectors (ISO 80369-1:2025, issued by both IEC and ISO), advancements in virucidal efficacy testing (EN 14476:2025), and accessibility requirements for persons with reduced mobility in railway settings (EN 16584-1:2025 and EN 16584-3:2025), this summary unpacks the month’s standards activity. Key themes include patient safety, infection control, and inclusive design. Professionals in design, quality management, procurement, and compliance will find retrospective analysis, actionable insights, and compliance guidance to align their processes with evolving international expectations. Explore the detailed highlights and access full standards via iTeh Standards to ensure your operations remain current and robust.

This monthly overview examines the standards published in October 2025 for the Health Care Technology sector, providing a comprehensive retrospective analysis. Focusing on EN 16585-3:2025—the latest in railway accessibility for persons with reduced mobility—this summary details important updates to equipment and component requirements on board rolling stock, including clearways and internal doors. Industry professionals, compliance officers, and quality managers will gain insights into sector trends, implementation guidance, and the significance of these developments for accessible transportation. This concise recap ensures you stay informed on critical regulatory shifts and evolving best practices impacting inclusive design in health care-related transport applications.

This monthly overview examines vital Health Care standards published in October 2025, providing analytical insights for professionals in the sector. Covering five newly released standards across laboratory data exchange, pandemic response infrastructure, ophthalmic device safety, dental instrument quality, and emergency resource management, this summary highlights prevailing themes such as digital transformation, patient safety, and readiness for public health crises. Discover how these standards reflect ongoing trends and challenges, including data interoperability, compliance with regulatory norms, and strengthened healthcare resilience. Professionals seeking to stay current with requirements, implementation strategies, and sector directions will find actionable guidance and curated backlinks for direct standard access within this comprehensive recap.

This monthly overview revisits the Health Care sector’s standards published in September 2025, offering in-depth analysis and context for professionals seeking to stay abreast of regulatory and technical developments. The article closely examines ISO 7376-2:2025, which establishes vital requirements for video laryngoscopes – a rapidly adopted tool in airway management. Key themes include enhanced patient safety, rigorous performance criteria, and harmonization with broader frameworks for anaesthetic and respiratory equipment. This comprehensive analysis outlines core requirements, user impacts, sector implications, and actionable guidance for compliance and implementation. Whether you are a healthcare provider, quality manager, or device manufacturer, this article distills the month’s most relevant standard, offering insights to inform procurement, compliance, and operational excellence in the evolving Health Care landscape.

This monthly overview examines the standards published in September 2025 for the Health Care Technology sector, summarizing five key documents that set terminology, safety, and material requirements for critical medical equipment. Covering areas such as respiratory care, MR safety labeling, implant materials, and radioactive source security, this recap identifies significant industry themes—standardization, patient safety, interoperability, and regulatory alignment. Professionals including quality managers, compliance officers, engineers, and procurement specialists will find this analysis invaluable for staying current, identifying emerging industry directions, and prioritizing compliance efforts. Ensure your organization does not miss essential updates impacting device labeling, clinical workflows, and procurement in health care technology.

This monthly overview examines the health care technology standards published in May 2025, providing industry professionals with critical insights and analysis. Covering five newly released standards, this article explores key updates in absorbable surgical implants, water-based dental cements, ophthalmic diagnostic instruments, and neural small-bore connectors. The review spotlights trends such as material innovation, patient safety, and performance verification, helping organizations understand their compliance obligations and the broader regulatory landscape. Whether you are a quality manager, engineer, compliance officer, or procurement professional, this summary offers valuable context, implementation guidance, and links to each standard on the iTeh Standards portal. Stay current on emerging issues and ensure your operations align with the latest international best practices by reviewing the most impactful standards from May 2025.

This comprehensive monthly overview examines five significant standards published for the Health Care Technology sector in May 2025—covering neural application connectors, lower limb prosthetics testing, ultrasonic surgical equipment measures, medical device radiation sterilization, and gravity-feed transfusion equipment. Industry professionals, compliance managers, and engineers will benefit from insights on evolving clinical safety, technical performance, compatibility, and harmonized regulatory approaches. The article identifies cross-cutting trends in standardization, practical compliance strategies, and why these standards will shape the future of patient safety and device reliability. Review this expertly curated roundup to ensure your organization’s approach to quality and technology remains current in a sector marked by constant innovation.

This monthly overview examines the standards published in May 2025 for the Health Care Technology sector, delivering valuable insights for quality managers, compliance officers, engineers, and industry professionals. Covering five critical standards, including ISO specifications on transfusion sets, chemical disinfection washer-disinfectors, AI in dental radiography, traditional Chinese medicine quality, and accessible systems for independent living, the article unpacks their scopes, key requirements, and industry implications. Discover how these standards respond to emerging trends like AI-driven diagnostics, infection prevention, accessibility, and global trade in medicinal products. Gain perspective on compliance priorities and integration strategies to ensure your organisation maintains best practices and regulatory alignment. Read the full summary for a comprehensive analysis of Health Care Technology standardization activity and its ongoing influence on quality, safety, and innovation.

All types of economic activity are regulated by the state where they are located, as well as by the relevant authorities. However, we can confidently talk about the existence of such sectors of the economy that are subject to stricter regulation than others. In particular, we are currently referring to the medical segment. Companies that manufacture medical equipment or medical supplies, or that provide medical services, bear increased responsibility for their actions. Such strictness is due to the fact that they directly interact with their patients and are responsible for their lives. Taking into account all the above factors, we advise you to study in detail the international standards that apply to medicine. On our site you can find a lot of useful information, in particular, some of the latest international medical standards, we have collected for you in this article. These documents will help you determine which aspects of your business you need to improve in order to bring them into compliance. After reading this text, at the end of the article you will be able to find active links to all the international standards we mention here.

Health care is that segment of the economy of a highly developed country, which is always given a significant amount of attention, since the well-being of the population depends on it. Therefore, manufacturers that operate in this segment must correctly assess the degree of responsibility that lies with their company. Medicine has made a big breakthrough over the past years, and accordingly, this has led to the emergence of new research methods, as well as new technologies for treating patients. Modern medicine quite often makes it possible to diagnose the problem in the early stages of the disease, which in turn significantly increases the success rate of cases of recovery. However, if we look at the situation from the point of view of medical equipment manufacturers, then we can see high competition among companies that are ready to provide the market with a high-quality and modern product. As a result, those companies that are able to quickly respond to changes, as well as adapt to the actual needs that exist on the market at a given time, turn out to be more competitive. Managers of such companies often ask themselves how they should properly organize the production processes in the company in order to meet the requirements. In order to answer this question, international standards have been created that regulate the field of health protection, and, accordingly, production in this area. Today we invite you to familiarize yourself with the main international standards that have been developed for this area with us. All documents were divided into categories, which in turn greatly simplifies orientation in them. We would like to emphasize once again that these documents will help you to organize the work of your company in such a way that you can provide the market with a product that will qualitatively differ from your competitors and help you gain leadership in your industry.

The possibilities of modern medicine have expanded significantly in our time, which means that the level of requirements that apply to it and to all related industries has also become higher. When a patient seeks help from a doctor of any specialization, he expects to receive qualified help from a specialist. He also wants to ensure that all procedures, including examinations and further treatment, will be carried out in accordance with international health standards, and without any additional threat to life. The main task of medicine, throughout the history of its existence, has been the preservation of human life. Consequently, medicine is a sector of the economy that is subject to strict regulation by the competent authorities. Given the high level of responsibility for all specialists who work in the field of medicine, it would be quite logical that in their work they will give preference to those tools that will be of high quality and meet all international standards. Thus, we understand that companies that manufacture medical equipment cannot ignore the requirements established by international standards in their work. As a rule, these documents in the field of medicine strictly regulate the requirements for ready-made instruments, as well as regulate production processes to ensure the sterility and safety of medical equipment. Due to the variety of medical specialties, there are already so many medical standards that govern the work of manufacturers, but they continue to be updated so that you can meet the current needs of the market. Today we invite you to familiarize yourself with some of the categories of international standards that relate to the production of medical equipment.

Nowadays technical development is constantly increasing pace of development. Moreover, every technological company is trying to focus its main area of ​​activity specifically on those parts of human life that can be primarily useful for the development of our planet on a global scale and in the long term. One of the most profitable, due to its constant demand, is the consumer sector of medicine, which includes both the production of medicines and the equipment necessary for the implementation of patient treatment processes. Medical research is gaining momentum in achieving unique means, and technology can extend people's lives for years to come. Old books about the fantastic possibilities of technology, including medical ones, are coming true like never before. Nevertheless, striving for the uniqueness of innovative achievements and patent profits, one should not forget that medicine is primarily aimed at saving human life, which is why this industry has a large number of international standards for enterprises that interact with various types of medical equipment and research activities, with which we will introduce you today.

The provision of medical services is a very complex and important process. Professionals who work in this area are responsible for the safety of the health of their patient. Given this moment, it becomes obvious how carefully they select the materials with which they will work in the future. Companies that manufacture medical supplies must be able to properly control the quality of the product they produce. It is worth making an additional emphasis on the fact that most of these materials are in direct contact with the patient’s body, so they must be completely safe for the body. The main task of the manufacturer of these products is to make sure that they do not contain any substances that could harm a person. The list of prohibited items can be very large and companies that work in the field of medical products need to know and follow it. Based on the importance of providing customers with safe and good products, new standards are constantly being created that regulate their quality. Today, we have prepared a material for you, in which we considered what requirements are for medical materials in the field of dentistry and ophthalmology, and also included information for you regarding testing systems. These documents will be useful for companies that manufacture products for medical activities.

Caring for human health has always been one of the most relevant areas and industries, which later began to develop as a business category. Most types of research and commercial activity in the field of medicine today are closely interconnected with innovative development as well as with financial results, which, as we can observe, influence global processes, especially over the past two years.  Since the health sector is one of the most unified, interaction with technology is not just a recommendation for accelerated development, but a necessity.  Consequently, there is a need for the formation of a scientific and technological base, which will significantly simplify the process of interaction both between organizations in different countries and between individual subjects of this industry.  Today, one of the most influential regulatory acts at the international level is the international standard.  Today we will acquaint you with some of the most significant documents in the field of operation of medical equipment and technologies.

The coronavirus has made its own adjustments to global plans, to the plans of economic financial systems, as well as to the development plans for scaling many businesses around the planet. Today, the prevailing number of organizations that have reached significant financial heights operate in the medical sector and make it possible to develop these industries at an ever faster pace. Nevertheless, one should not forget that oversaturation of the market in this industry can lead to an increase in the number of low-quality services and goods, and therefore directly affect the health of all mankind. That is why the number of medical companies is increasing and the number of norms and requirements, respectively, one of which are international standards.

International standardization is the engine of progress for both small and medium-sized businesses and entire corporations. Today the world is globalizing and the pace of interaction and business expansion is becoming more and more rapid. In order to constantly remain at the top of the so-called competition pyramid, it is necessary, first of all, to focus on the quality of the services provided and the goods produced. The same applies to the medical industry. But it should also be noted that one of the main criteria is the issue of safety and innovation awareness. When it comes to awareness, it should be noted that it is not only the latest equipment that is important, but also the international standardization that matches its implementation and use. Today we will introduce you to international documents that regulate the use of parts for medical equipment.

Product testing is one of the stages for the formation of a complete production cycle in which the final product or service will be presented in the highest quality manner. The same thing happens in the field of medicine, because when creating certain drugs or equipment, as well as services, it is necessary to carry out research stages. Since this industry is directly responsible for human health, the issue of testing, as well as the safety of molecular research testing, is regulated very seriously at many levels. One of these levels is international standardization. If your organization is in contact with medical research and the introduction of medical equipment or molecular research, we strongly recommend that you pay attention to the list of international standards below.

The pace of innovative development is sometimes quite impressive and requires constant staff development in order to quickly adapt to the introduction of new technologies. Today, one of the main issues on a global scale is the issue of the health of each person, which is why all investments and mainly basic scientific and technical research are aimed at creating medical equipment that greatly simplifies the solution of emerging problems in medicine as a whole. In order for each company that comes into contact with the field of medicine to have high-quality equipment, and also to bear full responsibility for the activities carried out, such regulatory legal acts as international standards are being created, with the main ones for medical equipment we will introduce you today.

In the modern world, medical equipment is more and more exposed to the introduction of innovations and the automation of all processes.  Despite the fact that a huge number of technologies and new uses for old equipment are increasing every day, human labor in the field of medicine cannot be completely replaced today.  When it comes to human health, there is a need to create a huge number of regulatory documents that regulate the implementation of innovations and the operation of existing equipment, as well as the general principles for the application of international standards.  One of the most popular documents of this type today are ISO standards, with the last of which we will introduce you today.

The field of drug is developing progressively more reliably, with respect to the field of human activity, which is at risk for the security of life and the protection of prosperity, understand that a colossal commitment is constrained both on each person who works around here and on the stuff that used. To tie together the game plan of usage of headways in medicine, unprecedented managerial legitimate showings are made that immediate all of the features and concentrated limits. Unquestionably the most basic records of this sort are worldwide standards. Since any piece of human activity is making at an accelerated speed, the invigorating of worldwide rules is a need in case you come into contact or work in the field of medicine. Today we give you an overview of presumably the most recent and current worldwide rules for clinical devices.

Medical equipment is quite diverse in terms of the methods of its use, as well as the complexity of using and implementing updates. Recently, an increasing amount of artificial intelligence is being introduced into any type of equipment, thereby facilitating the possibility of its use, but on the other hand, complicating and lengthening the adaptation process. It is in order for the introduction of innovations to become the safest, to minimize possible physical financial risks and also to create a unified system at the international level, regulatory documents are being created that regulate the aforementioned processes. Today we want to introduce you to the international ISO standards for cardiac equipment. If your field of activity comes into contact with this type of equipment, we strongly recommend staying up to date with the latest developments in the field of international standardization to be sure of the complete safety of existing processes in your production or organization.

In the age of modern technology, many corporations focus on the development of innovations related to the improvement of production aspects. But nevertheless, human health remains at the forefront of the key issues of modern problems. Since this aspect in the context of the engine of progress is the main one, then all financial markets and their development form new trends. To regulate most of the issues arising in the field of medicine, international standards are created, which are responsible for the creation of a single system of safety and quality. Today we will acquaint you with some of the latest documents that will help your business reach international scale in the most harmonious and productive way.

Technological development in every area of people’s lives significantly increases its pace. More than that overwhelming majority of organizations and companies tend to invest in investigations and own laboratories. The general characteristic of the innovation market can be described as a word diverse, but at the same time the diversity of technologies needs to be strongly regulated. As far as medical sector has widen the boundaries of emergency and development of innovation inside this specific field, the demand for international regulatory documents has increased. Today we will familiarize you with the latest updates in the international standardization sphere for medical industry.

Human health is precisely the very aspect that cannot be predicted and it is impossible to give an accurate assessment of the development of events. As the last year has shown, the field of medicine has a huge impact not only on the framework in which it functions, but also on the functioning of any other world system, both economic and financial. Due to the fact that every day today more and more industries and businesses appear in this industry, then the number of regulatory documents regulating this activity is also increasing. Below we will provide you with a list of the most relevant international standards for the use and manufacture of medical devices today. We hope that this information will be the beginning of a new stage in the development of your organization.

Despite the proliferation of wireless technologies and the constant movement towards innovative development, the transmission of electricity and power by wire is still widely used today. Since this category of technologies is the most global one, a single scientific and technological base is created for the entire system and is the same for all countries of the world to create clear instructions for use, implementation, and troubleshooting. In order for the use of the above technologies to be carried out in the safest way and also to bring the most productive results from their operation, it is necessary to follow the rules and regulations prescribed in international standards. Since cables and the accompanying equipment are used in every area of ​​human activity, we recommend that you be aware of the international regulations that govern them.

Over the past year, the issue of medicine and the use of medical equipment has been gaining more and more popularity every day. It should be noted that the increase in the use of devices in the field of medicine implies a directly proportional increase in the number of standards that regulate these processes at the international level. Since in this industry quality is responsible for the preservation of people's health, it is necessary to pay very important attention to the norms that minimize the risks of negative consequences. Today we will introduce you to the standards for the use of medical equipment, which you must have in place if your areas of activity are even slightly in contact with medicine.

In the light of recent events on the world stage, the production and use of protective medical equipment has increased significantly. It should be noted that with the emergence of increased demand, the number of proposals and production in this area also increased. Since the main issue of quality is responsible for human lives, the standardization of this aspect has become much stricter, more and more norms and standards arise every day.
Compliance with international rules in the field of production, sale and use of protective equipment can affect not only the level of demand for your products both in the domestic and foreign markets, but also on the company's image, which will determine the further vector of the company's development. Today, we will introduce you to the most basic international standards applicable to medical protective equipment.

Today, medicine is one of the most sought-after areas in the life of the whole planet.  More and more business services arise associated with it, which is why compliance with correct international standards is mandatory. That is why we strongly recommend to stay up to date with the latest developments and updates in the field of international standards. More than that we emphasize on the fact that standards can be applicable for manufacturers both of medical equipment, parts and appliances, they can also be important for environmental issues and home usage.