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Chemical Measurement Integrity: Advanced Quality Assurance

05 – 09 Jan. 2026, Abu Dhabi23 – 27 Nov. 2026, Sharm El Shaikh

COURSE OVERVIEW:

The meaning of this course lies in the pursuit of absolute reliability in chemical results through the application of advanced quality assurance frameworks. In a modern laboratory, measurement integrity is the foundation upon which critical health, safety, and economic decisions are made. This course explores the philosophical and mathematical underpinnings of why we trust a number, moving beyond basic checks to a comprehensive system of technical verification.

 

The scope of this training involves the deep integration of ISO 17025 requirements with practical laboratory operations. It addresses the management of measurement uncertainty, the selection of appropriate reference materials, and the rigorous validation of complex analytical methods. By focusing on the "Total Quality" approach, participants will learn how to identify latent risks in the measurement process that traditional quality control might overlook.

 

The coverage includes the design of inter-laboratory comparisons, the use of control charts for trend analysis, and the implementation of blind testing protocols. Participants will explore the nuances of traceability to the International System of Units (SI) and the role of peer review in result validation. This course provides the strategic tools necessary to maintain a laboratory’s reputation for excellence and to ensure that all chemical data is legally and scientifically defensible.

 

COURSE OBJECTIVES:

After completion of this course, the participants will be able to:

  • Define the core principles of measurement integrity in an analytical context.
  • Apply advanced statistical tools to monitor laboratory performance over time.
  • Design a comprehensive Quality Assurance (QA) plan for multi-disciplinary labs.
  • Evaluate the traceability of chemical measurements to international standards.
  • Implement rigorous protocols for the selection and use of Certified Reference Materials.
  • Conduct root cause analysis for significant analytical deviations or outliers.
  • Develop internal proficiency testing schemes to challenge laboratory staff.
  • Calculate expanded measurement uncertainty for complex chemical assays.
  • Manage the transition from manual quality checks to automated QA software.
  • Audit the technical competence of personnel through documented performance metrics.
  • Validate the integrity of electronic data captured from analytical instrumentation.
  • Formulate strategies for continuous improvement based on quality indicators.

 

TARGET AUDIENCE:

This course is intended for Quality Managers, Senior Chemists, Laboratory Directors, and Technical Auditors who are responsible for ensuring the highest levels of accuracy and compliance in chemical testing.

 

TRAINING COURSE METHODOLOGY:

A highly interactive combination of lectures, discussion sessions, and case studies will be employed to maximize the transfer of information, knowledge, and experience. The course will be intensive, practical, and highly interactive. The sessions will start by raising the most relevant questions and motivating everybody to find the right answers. The attendants will also be encouraged to raise more of their questions and to share in developing the right answers using their analysis and experience. There will also be some indoor experiential activities to enhance the learning experience. Course material will be provided in PowerPoint, with necessary animations, learning videos, and general discussions.

 

The course participants shall be evaluated before, during, and at the end of the course.

 

COURSE CERTIFICATE:

National Consultant Centre for Training LLC (NCC) will issue an Attendance Certificate to all participants completing a minimum of 80% of the total attendance time requirement.

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