The concept of process monitoring and improvement applies to any type of industry: automotive, textiles, food, pharmaceuticals, biologics, medical devices, electronics, aerospace, banking, educational institutions, service providers, and so on. The focus of this book is to identify and apply different process monitoring and improvement tools in any organization. This book is aimed at engineers, scientists, analysts, technicians, managers, supervisors, and all other professionals responsible to measure and improve the quality of their processes. Many times, these professionals do not have a formal education on the use of these tools but learn about them throughout the different improvement projects in which they are involved in their work environment. This book is intended to fill the gap between the lack of formal education in the tools and the need to implement those tools in an improvement project. The book can also be used as a refresher course for those professionals who did learn about these tools as part of their educational background.
The purpose of this handbook is to assist individuals for the Certified Pharmaceutical Good Manufacturing Practices Professional (CPGP) examination and provide a reference for the practitioner. The second edition reflects the Body of Knowledge which was updated in 2015. This edition has also incorporated additional information including updated references. The updates reflect the current trends and expectations of the evolving pharmaceutical industry driven by consumer expectations and regulatory oversight. This handbook covers compliance with good manufacturing practices (GMPs), as regulated and guided by national and international agencies for the pharmaceutical industry. It covers finished human and veterinary drugs and biologics, and combination devices, as well as their component raw materials (including active pharmaceutical ingredients (APIs) and excipients), and packaging and labeling operations.
Target MH-CET contains the detailed solutions of MH-CET 2007 to 2018. The solution to each and every question has been provided. The past papers will guide you in terms of what has been asked in the earlier years. Thus in all there are 10 past papers as the MH-CET paper was not held in 2013. This is followed by 5 Mock tests designed exactly as per the pattern of the 2018 MH-CET exam. Each Mock Test contains 200 questions on the 4 sections: Section I: Verbal Ability & Reading Comprehension (50) Section II: Quantitative Aptitude (50) Section III: Logical & Abstract Reasoning (100)
This comprehensive, standard work has been updated to remain an important resource for all those needing detailed knowledge of the theory and applications of vacuum technology. The text covers the existing knowledge on all aspects of vacuum science and technology, ranging from fundamentals to components and operating systems. It features many numerical examples and illustrations to help visualize the theoretical issues, while the chapters are carefully cross-linked and coherent symbols and notations are used throughout the book. The whole is rounded off by a user-friendly appendix of conversion tables, mathematical tools, material related data, overviews of processes and techniques, equipment-related data, national and international standards, guidelines, and much more. As a result, engineers, technicians, and scientists will be able to develop and work successfully with the equipment and environment found in a vacuum.
Clinicians who work on the frontlines of correctional mental health know that the challenges are only increasing. Not only is the proportion of inmates with mental disorders growing at a rate that exceeds that of the correctional population as a whole, but this group is expanding at both ends of the aging continuum, so that increasing numbers of both geriatric and juvenile offenders require assessment and treatment. Changing patient demographics and evolving treatment modalities make it essential that psychiatrists, psychologists, social workers, nurses, and other professionals who serve the prison population have access to the most practical, up-to-date, and comprehensive resource. Handbook of Correctional Mental Health, now in an expanded, second edition, is that resource. This book addresses key concepts to ensure that the reader meets the current standard of care for inmates through all phases of the criminal justice system. In 20 state-of-the-art chapters, nationally recognized providers and correctional mental health experts address the most pressing issues facing clinicians. Unique to this edition, the Handbook: Summarizes the literature regarding unique populations observed in a correctional environment, thereby assisting the provider in tailoring treatment to various target populations. Provides a clear overview of both malpractice law and the concept of "deliberate indifference" that aids the reader in understanding the legal requirements for providing care and minimizing risks of lawsuits. Educates clinicians on how to differentiate feigned versus legitimate mental health symptoms, and how to understand and interpret inmate motivations for psychiatric malingering. Discusses important administrative aspects regarding documentation issues, quality assurance, and practicing under a consent decree. Provides useful tables throughout the text with key summary points emphasized. Includes five new, clinically focused chapters on the assessment and treatment of inmates with substance use disorders, geriatric offenders, juvenile offenders, inmates with self-injurious behaviors, offenders who have experienced various traumas during their lives, and inmates housed on maximum security units and death row. Other titles in the field are either out-of-date or limited in scope. By contrast, this new edition of Handbook of Correctional Mental Health includes everything mental health professionals need to provide the highest standard of care to this growing -- and complex -- patient population.
Written by experienced process improvement professionals who have developed and implemented computer based systems in organizations around the world, Interpreting the CMMI: A Process Improvement Approach, Second Edition provides you with specific techniques for performing process improvement. Employing everyday language and supported by real world
First published in 1995, the award-winning Civil Engineering Handbook soon became known as the field's definitive reference. To retain its standing as a complete, authoritative resource, the editors have incorporated into this edition the many changes in techniques, tools, and materials that over the last seven years have found their way into civil
For quality professionals and manufacturers in the food safety and medical device industries, risk management is essential to ensuring organizations meet FDA regulations and requirements. Without these recognized standards, the lives of patients and consumers are placed in jeopardy. In this third edition of Quality Risk Management in the FDA-Regulated Industry, Jose Rodriguez-Perez provides an updated view of the risk management field as it applies to FDA-regulated products using risk-based thinking.
For many years, we considered human errors or mistakes as the cause of mishaps or problems. In the manufacturing industries, human error, under whatever label (procedures not followed, lack of attention, or simply error), was the conclusion of any quality problem investigation. The way we look at the human side of problems has evolved during the past few decades. Now we see human errors as the symptoms of deeper causes. In other words, human errors are consequences, not causes. The basic objective of this book is to provide readers with useful information on theories, methods, and specific techniques that can be applied to control human failure. It is a book of ideas, concepts, and examples from the manufacturing sector. It presents a comprehensive overview of the subject, focusing on the practical application of the subject, specifically on the human side of quality and manufacturing errors. In other words, the primary focus of this book is human failure, including its identification, its causes, and how it can be reasonably controlled or prevented in the manufacturing industry setting. In addition to including a detailed discussion of human error (the inadvertent or involuntary component of human failure), a chapter is devoted to analysis and discussion related to voluntary (intentional) noncompliance. Written in a direct style, using simple industry language with abundant applied examples and practical references, this books insights on human failure reduction will improve individual, organizational, and social well-being.
