About Cabling Installation & Maintenance

Our mission: Bringing practical business and technical intelligence to today's structured cabling professionals

For more than 30 years, Cabling Installation & Maintenance has provided useful, practical information to professionals responsible for the specification, design, installation and management of structured cabling systems serving enterprise, data center and other environments. These professionals are challenged to stay informed of constantly evolving standards, system-design and installation approaches, product and system capabilities, technologies, as well as applications that rely on high-performance structured cabling systems. Our editors synthesize these complex issues into multiple information products. This portfolio of information products provides concrete detail that improves the efficiency of day-to-day operations, and equips cabling professionals with the perspective that enables strategic planning for networks’ optimum long-term performance.

Throughout our annual magazine, weekly email newsletters and 24/7/365 website, Cabling Installation & Maintenance digs into the essential topics our audience focuses on.

  • Design, Installation and Testing: We explain the bottom-up design of cabling systems, from case histories of actual projects to solutions for specific problems or aspects of the design process. We also look at specific installations using a case-history approach to highlight challenging problems, solutions and unique features. Additionally, we examine evolving test-and-measurement technologies and techniques designed to address the standards-governed and practical-use performance requirements of cabling systems.
  • Technology: We evaluate product innovations and technology trends as they impact a particular product class through interviews with manufacturers, installers and users, as well as contributed articles from subject-matter experts.
  • Data Center: Cabling Installation & Maintenance takes an in-depth look at design and installation workmanship issues as well as the unique technology being deployed specifically for data centers.
  • Physical Security: Focusing on the areas in which security and IT—and the infrastructure for both—interlock and overlap, we pay specific attention to Internet Protocol’s influence over the development of security applications.
  • Standards: Tracking the activities of North American and international standards-making organizations, we provide updates on specifications that are in-progress, looking forward to how they will affect cabling-system design and installation. We also produce articles explaining the practical aspects of designing and installing cabling systems in accordance with the specifications of established standards.

Cabling Installation & Maintenance is published by Endeavor Business Media, a division of EndeavorB2B.

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EU Regulations for Digital Medical Devices with AI Components Specialist Course | A Basket Full of Requirements - What Does a Manufacturer Need to Consider? (ONLINE EVENT: October 7, 2025) - ResearchAndMarkets.com

The "The EU Regulations for Digital Medical Devices with AI Components - A Basket Full of Requirements - What Does a Manufacturer Need to Consider?" training has been added to ResearchAndMarkets.com's offering.

This compact 4-hour specialist course provides manufacturers, developers and quality managers with a systematic overview of the regulatory requirements that must be observed when developing and placing AI-based medical software on the market in Europe.

In addition to EU MDR 2017/745, numerous other EU regulations and national regulations apply to the development, approval and documentation of digital medical devices with AI components, the sheer number of which can make even well-informed manufacturers and developers lose track. In addition, various legal deadlines expire or have already expired by 2031, with further requirements to be met with each deadline. For example, the AI Act is already legally binding and applicable, while the regulations on the European Health Data Space (EHDS) have several transitional periods.

It is also often unclear what exactly the legislator means by a digital medical device and how an AI component affects the requirements. It should also be borne in mind that digital products that become part of a critical infrastructure must comply with the NIS2 Directive or the KRITIS Umbrella Act. This seminar systematically guides you through the requirements for digital medical devices with AI components in the regulatory role of manufacturer and contract developer. It provides you with a structured approach on how to comply with and apply the current and future regulations.

The development and marketing of digital medical devices with AI components is subject to numerous European regulations. In addition to the EU Medical Device Regulation (MDR), the AI Act, data protection requirements (GDPR) and standards such as IEC 62304, ISO 14971 and ISO/IEC 42001 are increasingly coming into focus.

Why Should You Attend

You should attend this webinar to understand, what are the changes to the previous ISO 14971 and how to implement the changes in your risk management file in a simple and quick way. Your implementation time can be shorter with a good plan and approach and need smart ideas to reach the right level to pass the expectation by your certification company or notified body.

Who Should Attend:

  • Manufacturers and developers of digital medical devices
  • Regulatory affairs managers
  • Quality managers
  • Technical project managers and software architects

Key Topics Covered:

What is a digital medical device with an AI component?

  • Definition of the term from the perspective of various applicable regulations.
  • Comparison of different terms and definitions.
  • Definition and differentiation from digital health applications (DiGA)

Where can the requirements for digital medical devices be found in the EU MDR 2017/745?

which other EU regulations and EU directives apply?

  • AI Act, Data Act, Data Governance Act, EHDS Act, GDPR, NIS-2, new Product Liability Directive.

Which mandatory harmonized standards apply?

How do the various regulations interact and what impact does this have on the development and approval process and product documentation?

Transitional periods

  • When do which transition periods expire and what does this mean for manufacturers and operators of digital medical devices?
  • A parallel overview of the deadlines for all the regulations discussed here

Speakers:

Prof. Dr. h.c. Frank Stein

Senior Medical Device Expert

Nemius Consulting GmbH

Dr. h.c. Frank Stein, medical engineer, medical engineering experience since 25 years, clinical and research experience in cardiac surgery and cardiology, industrial experience in ophthalmology, neurology, traumatology and dental implants, active implants, active devices, international project and regulatory consulting experience in Europe, North-America, Asia, Australia, Arabic Countries, Latin-America.

For more information about this training visit https://www.researchandmarkets.com/r/4kqcev

About ResearchAndMarkets.com

ResearchAndMarkets.com is the world's leading source for international market research reports and market data. We provide you with the latest data on international and regional markets, key industries, the top companies, new products and the latest trends.

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