Clean Room Technology PDF Download

Author: James W. Useller
Publisher:
ISBN:
Category : Clean rooms
Languages : en
Pages : 80

View

Book Description

Author: Zhonglin Xu
Publisher: Springer Science & Business Media
ISBN: 3642393748
Category : Technology & Engineering
Languages : en
Pages : 871

View

Book Description
Fundamentals of Air Cleaning Technology and Its Application in Cleanrooms sets up the theoretical framework for cleanrooms. New ideas and methods are presented, which include the characteristic index of cleanrooms, uniform and non-uniform distribution characteristics, the minimum sampling volume, a new concept of outdoor air conditioning and the fundamentals of leakage-preventing layers. Written by an author who can look back on major scientific achievements and 50 years of experience in this field, this book offers a concise and accessible introduction to the fundamentals of air cleaning technology and its application. The work is intended for researchers, college teachers, graduates, designers, technicians and corporate R&D personnel in the field of HVAC and air cleaning technology. Zhonglin Xu is a senior research fellow at China Academy of Building Research.

Author: Matts Ramstorp
Publisher: John Wiley & Sons
ISBN: 3527613137
Category : Science
Languages : en
Pages : 179

View

Book Description
Contamination control is being used by more and more industries where the highest level of cleanliness and hygiene is of vital importance. This book covers the basic principles of contamination control and cleanroom technology from a holistic point of view. It deals with cleanliness and hygiene and their effects on the outcome of a process, reflecting the latest results from both scientific and practical points of view. The following topics are covered: contaminants and how they are measured cleanrooms and clean zones cleaning and decontamination cleanroom clothing the impact of people on cleanliness. Intended as an introduction to the area of contamination control, the text is also an excellent source of knowledge for people with both theoretical and practical experience. The Swedish version has been used for a long time within the Nordic countries as a basic training textbook within the pharmaceutical, microelectronics, food and beverage, optics and many other industries.

Author: Tim Sandle
Publisher: Elsevier
ISBN: 0443216010
Category : Medical
Languages : en
Pages : 510

View

Book Description
Biocontamination Control for Pharmaceuticals and Healthcare outlines a biocontamination strategy that tracks bio-burden control and reduction at each transition in classified areas of a facility. The first edition of the book covered many of the aspects of the strategy, but the new official guidance signals that a roadmap is required to fully comply with its requirements. Completely updated with the newest version of the EU-GPM (EN17141) the new edition expands the coverage of quality risk management and new complete examples to help professionals bridge the gap between regulation and implementation. Biocontamination Control for Pharmaceuticals and Healthcare offers professionals in pharma quality control and related areas guidance on building a complete biocontamination strategy. - Includes the most current regulations - Contains three new chapters, including Application of Quality Risk Management and its Application in Biocontamination Control, Designing an Environmental Monitoring Programme, and Synthesis: An Anatomy of a Contamination Control Strategy - Offers practical guidance on building a complete biocontamination strategy

Author: Sandro C. Esteves
Publisher: CRC Press
ISBN: 1315355191
Category : Medical
Languages : en
Pages : 519

View

Book Description
Regulatory agencies worldwide have issued directives or such requirements for air quality standards in embryology laboratories. This practical guide reviews the application of clean room technology or controlled environments specifically suited for Assisted Reproductive Technology (ART) Units. Its comprehensive coverage includes material on airborne particles and volatile organic compounds, including basic concepts, regulation, construction, materials, certification, clinical results in humans, and more.

Author: Dr. Tim Sandle
Publisher: Grosvenor House Publishing
ISBN: 178148080X
Category : Health & Fitness
Languages : en
Pages : 284

View

Book Description
The Cleaning and Disinfection handbook is aimed at those working within the pharmaceutical and healthcare sectors around the world, as well as providing valuable information for students and for the general reader. The book provides comprehensive detail on different types of disinfectants and their modes of action; explains the problems of microbial destruction and resistance; introduces cleaning techniques and the latest safety regulations; expounds upon the application of cleaning within healthcare and pharmaceutical environments, noting current national and international standards. The book also provides guidance on disinfectant efficacy testing. Assembled by expert practitioners, the book balances theoretical concepts with sound practical advice, and is likely to become the definitive text on keeping contamination in control within clean areas and controlled environments. With this second edition, the book is fully updated in line with the latest standards and regulations.

Author: Anne Marie Dixon
Publisher: CRC Press
ISBN: 1420014854
Category : Medical
Languages : en
Pages : 254

View

Book Description
A critical technology in the science of contamination control, environmental monitoring is a technique that provides important data on the quality of a process, processing environment, and final product, which can aid scientists in identifying and eliminating potential sources of contamination in cleanrooms and controlled environments. In response

Author: W. Whyte
Publisher: John Wiley & Sons
ISBN:
Category : Technology & Engineering
Languages : en
Pages : 336

View

Book Description
12. The Production and Transmission of High Purity Gases for the Semiconductor Industry / R. Galbraith -- 13. Materials for Services Pipework / T. Hodgkiess.

Author: William Whyte
Publisher: John Wiley & Sons
ISBN: 0470748060
Category : Technology & Engineering
Languages : en
Pages : 382

View

Book Description
A self-contained and practical book providing step-by-step guidance to the design and construction of cleanrooms, appropriate testing methodologies, and operation for the minimization of contamination… This second edition has been comprehensively revised and includes extensive updates to the two chapters that contain information on cleanroom standards and guidelines. The chapter on risk management has been extensively revised, especially the section on risk assessment. Other new subjects that have been added to the various chapters are those on clean-build, determination of air supply volumes for non-unidirectional airflow cleanrooms, RABS (Restricted Access Barrier Systems), contamination recovery test methods, entry of large items into a cleanroom, glove allergy problems, and how to develop a cleanroom cleaning programme. Used for in-house training and a textbook in colleges, this volume is for cleanroom personnel at all levels. It provides novices with an introduction to the state-of-the-art technology and professionals with an accessible reference to the current practices. It is particularly useful in the semiconductor, pharmaceutical, biotechnology and life sciences industries. William Whyte is an international authority in cleanrooms, with over 45 years experience in research, teaching and consulting in the electronic, healthcare and pharmaceutical industries. He is a member of British and International standards committees writing the International Cleanroom standards, and has received numerous awards for his work in Cleanroom Technology. A comment on the first edition: "...extremely useful and helpful...very well-written, highly organized, easy to understand and follow..." (Environmental Geology, 2003)

Author: Charles Nehme
Publisher: Charles Nehme
ISBN:
Category : Technology & Engineering
Languages : en
Pages : 104

View

Book Description
In the fast-evolving world of electronics manufacturing, the role of clean rooms cannot be overstated. These controlled environments are essential for producing high-quality, reliable electronic components and devices, which are integral to nearly every aspect of modern life—from consumer electronics to medical devices, automotive systems, and aerospace technology. The primary function of a clean room is to minimize the introduction, generation, and retention of particles within the space. This is crucial because even microscopic contaminants can significantly impact the performance, reliability, and longevity of electronic components. Clean rooms are designed to maintain extremely low levels of particulate matter, achieved through stringent control over air filtration, pressure, temperature, and humidity. Importance of Clean Rooms in Electronics Manufacturing Contamination Control: Electronic components, particularly semiconductors, are highly sensitive to dust, bacteria, and other airborne particles. Clean rooms ensure that these contaminants are kept at bay, protecting the integrity of the manufacturing process. Quality Assurance: The use of clean rooms helps in maintaining the high standards required in electronics manufacturing. This translates to fewer defects, higher yields, and better performance of the final products. Compliance with Standards: Many sectors, especially those involving medical devices and aerospace technology, have stringent regulatory requirements. Clean rooms help manufacturers comply with these standards, ensuring that their products are safe and reliable. Innovation and Precision: Advanced electronics manufacturing often involves nanotechnology and microelectronics, where precision is paramount. Clean rooms provide the controlled environment necessary for such high-precision work. Key Elements of a Clean Room Air Filtration Systems: High-Efficiency Particulate Air (HEPA) filters and Ultra-Low Penetration Air (ULPA) filters are used to remove particles from the air, ensuring that the environment remains contaminant-free. Controlled Environment: Parameters such as temperature, humidity, and pressure are meticulously controlled to prevent any adverse effects on the manufacturing process. Clean Room Classifications: Clean rooms are classified based on the number and size of particles permitted per volume of air. The most common classification standards are those of the International Organization for Standardization (ISO). Personnel and Equipment Protocols: Strict protocols for personnel, including the use of special clothing and hygiene practices, are essential. Similarly, equipment used in clean rooms is designed to minimize the generation of particles. Challenges and Considerations Cost: Establishing and maintaining clean rooms is expensive. This includes the cost of sophisticated filtration systems, environmental controls, and regular maintenance. Training: Personnel working in clean rooms require extensive training to understand and adhere to strict protocols. Technology Upgrades: As technology advances, clean rooms must be regularly updated to meet new standards and accommodate new manufacturing processes. Conclusion Clean rooms are indispensable in the realm of electronics manufacturing. They play a critical role in ensuring that the components and devices produced meet the highest standards of quality and reliability. As the industry continues to innovate and evolve, the importance of clean rooms will only grow, making them a cornerstone of modern manufacturing processes.