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

Tim Carli - Business Development Manager

Brayden Hudspeth - Sales Development Representative

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Analytical Method Validation, Verification and Transfer - 2 Day Virtual Seminar, Oct 7th- 9th, 2025 - ResearchAndMarkets.com

The "Analytical Method Validation, Verification and Transfer Virtual Seminar (Oct 7th - Oct 9th, 2025)" has been added to ResearchAndMarkets.com's offering.

Dependable analytical results are essential to making a knowledgeable choice about the excellence and care of the products in the medicinal business. Additionally, such investigative data is required for supervisory submissions in the provision of the drug creation recordings. Therefore, expressive untried projects including scheme appropriateness limits must be planned for the intended use of the process.

In this Analytical Method Validation Training Course, a general guideline for the determination of the analytical characteristics for different types of validation procedures is highlighted for the analysis of both the drug substance and drug product. The factors to consider for verification of the compendial procedures will also be discussed.

In addition, different approaches for the transfer of analytical procedures from one lab (transferring) to another lab (s) (receiving) under different circumstances will be covered. Other related topics for obtaining reliable data will also be discussed. These topics include analytical instrument qualification as well as how to set, handle and monitor specifications.

In this Analytical Method Validation Training Course, the overall recommendation for the purpose of the logical features for diverse types of authentication measures is highlighted for the examination of the drug substance and drug product. The trainees will be required to pay attention to the influences to reflect for confirmation of the compendial actions that are an indivisible part of the training course. In addition, different methods for the transmission of the analytical procedures from one lab (transferring) to another lab (s) (receiving) under different conditions will be enclosed. Other related topics for obtaining reliable data will also be discussed. These themes comprise logical tool requirements as well as how to set, grip and screen specifications.

Learning Objectives

The Analytical Method Validation Training Course follows a few objectives that every aspiring candidate needs to focus on while undergoing the course:

  • Drug Endorsement Process and Controlling Necessities (secluded values)
  • Substitute Official methods and options
  • Allowed Alterations of Chromatographic System Strictures
  • Pharmacopeias and Compendial Approval Process (public standards)
  • Logical Method Life Cycle
  • Investigative Method Authentication
  • Compendial Coordination Procedure
  • Analytical Instrument Qualifications including DQ, IQ, OQ, PQ
  • Analytical Method Verification
  • Analytical Method Transfer
  • Chromatography System Appropriateness Necessities
  • Analytical Method Validation
  • How to Set Specifications and how to handle out-of-specification (OOS) and out-of-trend (OOT) results

Who Should Attend:

  • Contract Laboratories (CRO), Academia (pharmacy, Pharmaceutical Industry, Pharmaceutical, Chemistry), government (FDA or regulatory authorities)
  • Quality Analysis Managers and Personnel
  • Controlling Personnel
  • Analytical and or Formulation Chemists
  • Quality Control Managers and Personnel
  • Lab Supervisors and Managers
  • Compendial Liaisons
  • Senior or Graduate students (chemistry, pharmaceutical, pharmacy)
  • Pharmaceutical scientists/Pharmacists working in Industry

Course Agenda:

  • Seminar objectives review, expectations, and scope.
  • Pharmacopoeias and Compendial (USP) Approval Process (public standards)
  • Analytical Method Validation (typical validation parameters)
  • Drug Approval Process and Regulatory (FDA) Requirements (private standards)
  • Chromatography System Suitability Requirements
  • Compendial Harmonization Process
  • Qualification Phases (DQ, IQ, OQ, PQ)
  • Precision/Accuracy
  • Allowed Adjustments of Chromatographic System Parameters
  • Specificity
  • Factors to Consider
  • LOD and LOQ
  • Analytical Method Verification
  • Analytical Instrument Qualifications
  • Analytical Method Transfer
  • Linearity/Range
  • FDA and USP Requirements
  • Instrument Categories
  • Different Approaches
  • Summary and Review
  • Investigative Procedure Life Cycle
  • Setting Stipulations FDA rules and ICH strategies (Q6A)
  • Out-of-Specification (OOS)
  • Out of Trend (OOT)
  • How to handle OOS and OOT
  • Summary and Review

For more information about this training visit https://www.researchandmarkets.com/r/s7iobq

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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