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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Patrick McLaughlin

Serena Aburahma

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Peter Fretty - Vice President, Market Leader

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Digital Validation Demystified | GAMP 5 2.0 and CSA Integration Course - Elevating Compliance, Navigating FDA's Data Integrity Focus (ONLINE EVENT: September 18, 2025) - ResearchAndMarkets.com

The "Digital Validation Demystified - GAMP® 5 2.0 and CSA Integration" training has been added to ResearchAndMarkets.com's offering.

This course equips you with the tools, knowledge, and industry best practices necessary to optimize your approach to validation and compliance. Prepare to navigate FDA inspections with confidence and stay ahead of evolving regulatory requirements. This course is a transformative journey to revolutionize your approach to computer system validation and unlock unparalleled success in the ever-evolving landscape of FDA-regulated industries.

GAMP5, the global benchmark in computerized system validation since 2008, has evolved to meet the demands of cutting-edge technologies like Artificial Intelligence, Cloud Computing, and Agile Software Development, alongside regulatory advancements such as ICH Q9 and FDA's CSA initiative. The 2nd Edition of GAMP5 integrates crucial adaptations, emphasizing evolution over revolution, while addressing FDA's heightened scrutiny on data integrity during system validation inspections.

Gain invaluable insights into the nuances of Computer System Validation (CSV), System Development Life Cycle (SDLC) approaches, and 21 CFR Part 11 compliance for electronic records and signatures. Discover how to conduct comprehensive vendor audits to ensure the integrity of products and services delivered. With FDA's heightened focus on data integrity, learn essential strategies to safeguard structured and unstructured data throughout its life cycle. Understand the significance of risk assess...

Who Should Attend:

  • Information Technology Analysts
  • Information Technology Developers and Testers
  • QC/QA Managers and Analysts
  • Analytical Chemists
  • Compliance and Audit Managers
  • Laboratory Managers
  • Automation Analysts
  • Manufacturing Specialists and Managers
  • Supply Chain Specialists and Managers
  • Regulatory Affairs Specialists
  • Regulatory Submissions Specialists
  • Clinical Data Analysts
  • Clinical Data Managers
  • Clinical Trial Sponsors
  • Computer System Validation Specialists
  • GMP Training Specialists
  • Business Stakeholders/Subject Matter Experts
  • Business System/Application Testers
  • Vendors and consultants involved in validation and compliance

Key Topics Covered:

  • Identifying GxP Systems
  • GAMP5 Second Edition What's Different What's New?
  • Understanding GAMP5's impact on validation work
  • FDA requirements for Computer System Validation (CSV)
  • Learn about the System Development Life Cycle (SDLC) approach to validation
  • Data Integrity Assurance that supports GxP work
  • Assessment of a system's size, complexity, business criticality, GAMP5 category, and failure risk
  • Ensuring 21 CFR Part 11 compliance for electronic records and signatures
  • Preparing for an FDA inspection or audit of a GxP computer system
  • Conducting thorough vendor audits
  • Industry best practices based on risk assessment to ensure data integrity

Speaker

Carolyn Troiano has more than 30 years of experience in computer system validation in the pharmaceutical, medical device, animal health, tobacco and other FDA-regulated industries. She is currently an independent consultant, advising companies on computer system validation and large-scale IT system implementation projects.

During her career, Carolyn worked directly, or on a consulting basis, for many of the larger pharmaceutical companies in the US and Europe. She developed validation programs and strategies back in the mid-1980s, when the first FDA guidebook was published on the subject, and collaborated with FDA and other industry representatives on 21 CFR Part 11, the FDA's electronic record/electronic signature regulation.

Carolyn has participated in industry conferences. She is currently active in the PMI, AITP, and RichTech, and volunteers for the PMI's Educational Fund as a project management instructor for non-profit organizations.

For more information about this training visit https://www.researchandmarkets.com/r/8duxrm

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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