Industrial quality control

This title presents industry-oriented case studies and solution frameworks addressing operational challenges across the textile, apparel, and fashion value chain.

This title presents industry-oriented case studies and solution frameworks addressing operational challenges across the textile, apparel, and fashion value chain.

The book "e;Lean Motion and Time Study: Continuously Improving Work Design through Methods Engineering"e; was conceived as a guide for academics and professionals seeking to achieve sustainable process efficiency.

In engineering and quality control, various situations, including process validation and design verification, require equivalence and noninferiority tests.

Originally designed to address safety concerns, Failure Mode and Effect Analysis (FMEA) is now used throughout the industry to prevent a wide range of process and product problems.

This book provides guidelines for obtaining research and development (RD) results of a consistent and known quality.

Sterile Drug Products: Formulation, Packaging, Manufacturing, and Quality teaches the basic principles of the development and manufacture of high quality sterile dosage forms.

The demands of the global economy require manufacturers to produce highly reliable and easily maintainable engineering products.

Dietary Supplement GMP is a one-stop how-to road map to the final dietary supplement GMP regulations recently issued by the FDA covering the manufacture, packaging, and holding of dietary supplement products.

This book is a handy source for comprehending reliability concepts, interpreting reliability requirements, and understanding reliability reports.

The true promise and benefits of Supply Chain Management elude many organizations.

Contamination problems have become a major factor in determining the manufacturability, quality, and reliability of electronic assemblies.

Applications, Processes, and Controls is the second volume in the Handbook for Critical Cleaning, Second Edition.

La Gestión de Activos Físicos es un campo de acción emergente en la industria que presta una atención renovada a la estrategia de las operaciones y mantenimiento con una visión a largo plazo.

Pharmaceutical product development is a multidisciplinary activity involving extensive efforts in systematic product development and optimization in compliance with regulatory authorities to ensure the quality, efficacy and safety of resulting products.

Performing statistical analysis for Lean Six Sigma DMAIC projects has never felt this effortless—or this elegant.

This work sets out to explore the "e;aggregates"e; field in a comprehensive manner, from natural deposits to finished products.

This work sets out to explore the "e;aggregates"e; field in a comprehensive manner, from natural deposits to finished products.

This comprehensive book examines the manufacturing of thin-walled structures using diverse Additive Manufacturing (AM) processes.

This comprehensive book examines the manufacturing of thin-walled structures using diverse Additive Manufacturing (AM) processes.

Enterprise-Grade Test Automation PlaybookBest Practices for Architecture, Governance, and Scale - With production-ready code and research-backed patterns Why do most test automation initiatives fail?

Serving as a foundational guide to the field, this book is an essential resource for professionals involved in the development of mechanical systems and related industries.

This groundbreaking book introduces the Quality Life Cycle Assessment (QLCA) model - a novel approach that integrates product quality assessment and life cycle assessment (LCA) in sustainable manufacturing.

Serving as a foundational guide to the field, this book is an essential resource for professionals involved in the development of mechanical systems and related industries.

This groundbreaking book introduces the Quality Life Cycle Assessment (QLCA) model - a novel approach that integrates product quality assessment and life cycle assessment (LCA) in sustainable manufacturing.

This book presents statistical methods applied to textile and apparel manufacturing processes.

This book presents statistical methods applied to textile and apparel manufacturing processes.

Best used in combination with The ASQ Certified Supplier Quality Professional Handbook, Second Edition, this study guide offers targeted practice for any candidate preparing for the ASQ Certified Supplier Quality Professional (CSQP) examination.

Zeit scheint so selbstverständlich – und ist doch eine der größten menschlichen Fiktionen.

La termografia infrarroja (TT) es un metodo que obtiene imagenes de la distribucion del calor sobre la superficie del objeto ensayado.

Winner of the 2026 Shingo Publication Award and the 2026 International Lean Six Sigma Institute (ILSSI) book award!

Best used in combination with The ASQ Certified Supplier Quality Professional Handbook, Second Edition, this study guide offers targeted practice for any candidate preparing for the ASQ Certified Supplier Quality Professional (CSQP) examination.

The ASQ Certified Software Quality Engineer Handbook, Third Edition contains information and guidance that supports all the topics within the 2023 version of the Certified Software Quality Engineer (CSQE) Body of Knowledge (BoK).

Designed to aid candidates in preparing for ASQ Certified Quality Technician (CQT) certfication exam, this fourth edition aligns with the 2024 ASQ CQT Body of Knowledge (BoK).

Due to global competition, safety regulations, and other factors, manufacturers are increasingly pressed to create products that are safe, highly reliable, and of high quality.

Completely revised and updated, Fluid Sterilization by Filtration, Third Edition discusses the use of gas and fluid filtration systems in sterilization technology.

This title demonstrates how designed experiments are the most scientific, efficient, and cost effective method of data collection for validation in a laboratory setting.

Consider a Viable and Cost-Effective Platform for the Industries of the Future (IOF)Benefit from improved safety, performance, and product deliveries to your customers.

"e;Offers a comprehensive, unified presentation of statistical designs and methods of analysis for all stages of pharmaceutical development--emphasizing biopharmaceutical applications and demonstrating statistical techniques with real-world examples.

Through simple, practical approaches, Reliability Analysis and Prediction with Warranty Data: Issues, Strategies, and Methods helps Six Sigma black belts and engineers successfully interpret warranty data to make accurate predictions.

As quality becomes an increasingly essential factor for achieving business success, building quality improvement into all stages-product planning, product design, and process design-instead of just manufacturing has also become essential.

In today's sophisticated world, reliability stands as the ultimate arbiter of quality.

The normal or bell curve distribution is far more common in statistics textbooks than it is in real factories, where processes follow non-normal and often highly skewed distributions.

Describing NDE issues associated with real-world applications, this comprehensive book details conventional and forthcoming NDE technologies.

Spanning every critical element of validation for any pharmaceutical, diagnostic, medical device or equipment, and biotech product, this Second Edition guides readers through each step in the correct execution of validating processes required for non-aseptic and aseptic pharmaceutical production.

Demonstrates ways to track industrial processes and performance, integrating related areas such as engineering process control, statistical reasoning in TQM, robust parameter design, control charts, multivariate process monitoring, capability indices, experimental design, empirical model building, and process optimization.

Designed to aid candidates in preparing for ASQ Certified Quality Technician (CQT) certfication exam, this fourth edition aligns with the 2024 ASQ CQT Body of Knowledge (BoK).

This authoritative reference presents an up-to-date review of the testing methods, emerging technologies, and analytical systems and procedures used to prevent the microbial contamination of pharmaceutical processes, products, and environments.

A valuable tool for establishing and maintaining system reliability, overall equipment effectiveness (OEE) has proven to be very effective in reducing unscheduled downtime for companies around the world.