Download or read book Environmental Control Design of Clean Rooms written by and published by . This book was released on 1982 with total page 80 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Fundamentals of Air Cleaning Technology and Its Application in Cleanrooms written by Zhonglin Xu and published by Springer Science & Business Media. This book was released on 2013-10-10 with total page 871 pages. Available in PDF, EPUB and Kindle. Book excerpt: 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.
Download or read book Cleanroom Technology written by William Whyte and published by John Wiley & Sons. This book was released on 2010-03-01 with total page 382 pages. Available in PDF, EPUB and Kindle. Book excerpt: 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)
Download or read book Design Manual written by United States. Naval Facilities Engineering Command and published by . This book was released on 1973 with total page 296 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Clean Room Technology written by James W. Useller and published by . This book was released on 1969 with total page 80 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Biocontamination Control for Pharmaceuticals and Healthcare written by Tim Sandle and published by Elsevier. This book was released on 2024-01-28 with total page 510 pages. Available in PDF, EPUB and Kindle. Book excerpt: 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
Download or read book Handbook of Validation in Pharmaceutical Processes Fourth Edition written by James Agalloco and published by CRC Press. This book was released on 2021-10-28 with total page 1062 pages. Available in PDF, EPUB and Kindle. Book excerpt: Revised to reflect significant advances in pharmaceutical production and regulatory expectations, Handbook of Validation in Pharmaceutical Processes, Fourth Edition examines and blueprints every step of the validation process needed to remain compliant and competitive. This book blends the use of theoretical knowledge with recent technological advancements to achieve applied practical solutions. As the industry's leading source for validation of sterile pharmaceutical processes for more than 10 years, this greatly expanded work is a comprehensive analysis of all the fundamental elements of pharmaceutical and bio-pharmaceutical production processes. Handbook of Validation in Pharmaceutical Processes, Fourth Edition is essential for all global health care manufacturers and pharmaceutical industry professionals. Key Features: Provides an in-depth discussion of recent advances in sterilization Identifies obstacles that may be encountered at any stage of the validation program, and suggests the newest and most advanced solutions Explores distinctive and specific process steps, and identifies critical process control points to reach acceptable results New chapters include disposable systems, combination products, nano-technology, rapid microbial methods, contamination control in non-sterile products, liquid chemical sterilization, and medical device manufacture
Download or read book Environmental Monitoring for Cleanrooms and Controlled Environments written by Anne Marie Dixon and published by CRC Press. This book was released on 2016-04-19 with total page 254 pages. Available in PDF, EPUB and Kindle. Book excerpt: 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
Download or read book Monthly Catalogue United States Public Documents written by and published by . This book was released on 1983 with total page 1160 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Clean Rooms for Electronic Manufacturers Ensuring Precision and Reliability in Controlled Environments written by Charles Nehme and published by Charles Nehme. This book was released on with total page 104 pages. Available in PDF, EPUB and Kindle. Book excerpt: 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.
Download or read book Pharmacology of Ocular Therapeutics written by Thirumurthy Velpandian and published by Springer. This book was released on 2016-02-29 with total page 541 pages. Available in PDF, EPUB and Kindle. Book excerpt: This book comprises an integrated review of ocular therapeutics across all relevant fields. It addresses the real-world requirements of ophthalmologists, pharmacists and optometrists, as observed through working alongside these practitioners for two decades. Knowledge surrounding agents used in ophthalmic practice has, historically, been scattered. The book facilitates understanding of ocular drug therapy by compiling all key aspects of the pharmacology, toxicology, pharmaceutical science, ocular biochemistry and cell biology of these agents. Chapters detail drug transfer across barriers, systemic toxicity of topically applied drugs, autonomic drugs used for diagnostics, as well as anti-inflammatory, antiallergic, glaucoma and antimicrobial therapies, and avenues for the development of new ocular drugs. Applications of extemporaneously prepared formulations are described to inform day-to-day clinical practice. The use of mucoadhesive polymers in tear substitutes, ocular drug delivery systems, stem cell therapy, pharmacogenomics and antiangiogenic ocular chemotherapy are also explored. The book also provides insights from drugs of herbal origin, and a historical perspective on drugs for ocular use. Practicing and resident ophthalmologists, optometrists, pharmacists, nursing professionals, scholars in ocular drug research and students will equally benefit from this comprehensive guide.
Download or read book Parenteral Medications Fourth Edition written by Sandeep Nema and published by CRC Press. This book was released on 2019-07-19 with total page 1145 pages. Available in PDF, EPUB and Kindle. Book excerpt: Parenteral Medications is an authoritative, comprehensive reference work on the formulation and manufacturing of parenteral dosage forms, effectively balancing theoretical considerations with practical aspects of their development. Previously published as a three-volume set, all volumes have been combined into one comprehensive publication that addresses the plethora of changes in the science and considerable advances in the technology associated with these products and routes of administration. Key Features: Provides a comprehensive reference work on the formulation and manufacturing of parenteral dosage forms Addresses changes in the science and advances in the technology associated with parenteral medications and routes of administration Includes 13 new chapters and updated chapters throughout Contains the contributors of leading researchers in the field of parenteral medications Uses full color detailed illustrations, enhancing the learning process The fourth edition not only reflects enhanced content in all the chapters but also highlights the rapidly advancing formulation, processing, manufacturing parenteral technology including advanced delivery and cell therapies. The book is divided into seven sectionss: Section 1 - Parenteral Drug Administration and Delivery Devices; Section 2 - Formulation Design and Development; Section 3 - Specialized Drug Delivery Systems; Section 4 - Primary Packaging and Container Closure Integrity; Section 5 - Facility Design and Environmental Control; Section 6 - Sterilization and Pharmaceutical Processing; Section 7 - Quality Testing and Regulatory Requirements
Download or read book Monthly Catalog of United States Government Publications written by and published by . This book was released on 1983-08 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book FDA By lines written by and published by . This book was released on 1979-03 with total page 60 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Mesenchymal Stromal Cells written by Peiman Hematti and published by Springer Science & Business Media. This book was released on 2013-01-16 with total page 697 pages. Available in PDF, EPUB and Kindle. Book excerpt: Mesenchymal Stromal Cell (MSC) biology has been studied for more than 4 decades and the cells have been investigated for potential clinical applications for more than 15 years. Progress has become exponential over the past decade due mainly to the broad therapeutic potential of these cells. However, MSC studies have also been subject to controversy and increasing scrutiny as new mechanisms of action are reported and ever-expanding therapeutic applications pursued. In this book, leading authorities from all over the world, who are actively involved in this field, provide state-of-the-art knowledge of the basic biology, translational requirements and latest clinical experience with MSCs. This cutting edge book is the ideal resource for scientists and clinicians interested in pursuing an important and rapidly developing field of research that will eventually help patients and address urgent unmet medical needs. Features include: Coverage of the biology of MSCs, latest understanding of mechanisms of action, and role in tissue homeostasis and regeneration Identifying the potential of MSCs in proceeding from bench to bedside from regulatory , GMP production, ethical and safety aspects Critical analysis of clinical studies and the potential of MSCs to treat a wide variety of human diseases and tissues.
Download or read book Official Gazette of the United States Patent and Trademark Office written by and published by . This book was released on 2002 with total page 1524 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Applied Pharmaceutics in Contemporary Compounding written by Robert P. Shrewsbury and published by Morton Publishing Company. This book was released on 2015-01-01 with total page 465 pages. Available in PDF, EPUB and Kindle. Book excerpt: Applied Pharmaceutics in Contemporary Compounding, Third Edition is designed to convey a fundamental understanding of the principles and practices involved in both the development and the production of compounded dosage forms by applying pharmaceutical principles.
