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 MDR and FDA Clinical Evaluation of Medical Device Software and Software as a Medical Device Training Course (ONLINE EVENT: October 1, 2025) - ResearchAndMarkets.com

The "Clinical Evaluation of Medical Device Software and Software as a Medical Device Training Course" training has been added to ResearchAndMarkets.com's offering.

This course will provide a clear understanding of the clinical evaluation requirements and their practical application for software products, including AI/ML-based devices. It will also provide advice on how to determine the type and amount of data needed to sufficiently support the intended medical purpose and (individual) clinical claims, with many practical examples and analysis of differences between the EU MDR and FDA approach.

Whether developing new medical software for more precise diagnosis and targeted treatment or a healthcare app for individuals concerned about their health, manufacturers are tasked to appreciably prove to authorities the safety, quality, and effectiveness of their products.

The evaluation of clinical safety and performance, as well as the overall benefit-risk profile of the product, through a critical assessment of relevant data, is one of the key requirements for the manufacturers of medical device software and a focus area for regulators.

Benefits of attending

  • Gain an in-depth understanding of the requirements for clinical evaluation and how to apply them to different types of medical device software, including AI/ML-based devices
  • Understand how to establish measurable endpoints for clinical claims
  • Find out how to define and generate sufficient clinical and/or performance data to meet the safety and performance requirements of your software device
  • Witness the role of human factors and risks
  • Learn how to retrieve and use literature data effectively
  • Identify residual clinical risks and determine whether post-market clinical follow-up is required
  • Provide robust documentation in support of the clinical safety and performance of your device
  • Hear about frequent pitfalls of clinical regulatory submissions
  • Ensure continuing compliance throughout the software lifecycle

Certifications

  • CPD: 6 hours for your records
  • Certificate of completion

Who Should Attend:

  • Clinical and regulatory affairs professionals
  • Medical software R&D engineers and scientists
  • Product and programme managers
  • Quality assurance professionals

Key Topics Covered:

Introduction to clinical evaluation

  • The regulatory framework of gathering clinical evidence for devices and international differences (EU, US and UK.)
  • Clinical evaluation during the software lifecycle
  • Clinical vs performance evaluation
  • Definitions, purpose, deliverables
  • Process and key characteristics
  • Role of literature and state-of-the-art
  • Selecting data sources
  • Defining acceptance criteria
  • Evaluation of indirect benefits and risks

How to define a scope and a level of clinical evidence for medical device software

  • Validation of clinical association, technical performance and clinical performance
  • Role of validation and usability
  • Considerations for AI/ML - devices

Case studies - clinical evaluation of medical device software

Clinical trials and validation studies

  • Selecting appropriate study design and implications
  • Development and validation of AI/ML devices (cohort, case-control)
  • Clinical performance studies
  • Application of standards
  • Generating evidence of effectiveness
  • Evidence for Health Technology Assessment

Clinical trials and validation studies - continued

  • Reporting guidelines and checklists
  • Challenges of mHealth trials
  • Regulatory and ethical considerations

Clinical evaluation post-market

  • Implementing post-market clinical follow-up for medical device software
  • Real-world evidence

For more information about this training visit https://www.researchandmarkets.com/r/vz7re4

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.

Contacts

ResearchAndMarkets.com

Laura Wood, Senior Press Manager

press@researchandmarkets.com



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