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Pharmaceutical Facilities Plumbing Systems
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Book Synopsis Pharmaceutical Facilities Plumbing Systems by : Michael Frankel
Download or read book Pharmaceutical Facilities Plumbing Systems written by Michael Frankel and published by . This book was released on 2005 with total page 270 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Book Synopsis Facilities Site Piping Systems Handbook by : Michael L. Frankel
Download or read book Facilities Site Piping Systems Handbook written by Michael L. Frankel and published by McGraw Hill Professional. This book was released on 2013-02-05 with total page 513 pages. Available in PDF, EPUB and Kindle. Book excerpt: Complete and current coverage of site piping systems for facilities Featuring the latest codes and standards, this detailed resource discusses the design of facility piping systems that are installed on the site beyond the building wall. This is a comprehensive guide to the identification, measurement, transport, and disposal of various kinds of waterborne waste as well as to the supply of water and natural gas to facilities. Water conservation and reuse are also addressed. Written by a global expert in the field, this book provides the most up-to-date criteria and methods for the design of commercial, industrial, and institutional site facility systems. Facilities Site Piping Systems Handbook covers: Water wells Graywater Groundwater monitoring wells Water treatment Desalination Site domestic water service Site fire protection Site fuel gas systems Fats, oils, and grease interceptors, and motor oil separation units pH neutralization systems Infectious and biological waste drainage systems Nuclear waste Industrial waste Fire suppression water drainage Volatile liquids: treatment and disposal Stormwater harvesting and reuse Stormwater drainage and disposal Flow in ditches and open channels Sanitary gravity flow Pump discharge systems Underground piping design Freezing prevention of water and wastewater in exterior pipes and tanks Building rating and assessment systems
Book Synopsis Good Design Practices for GMP Pharmaceutical Facilities by : Terry Jacobs
Download or read book Good Design Practices for GMP Pharmaceutical Facilities written by Terry Jacobs and published by CRC Press. This book was released on 2016-08-19 with total page 535 pages. Available in PDF, EPUB and Kindle. Book excerpt: This revised publication serves as a handy and current reference for professionals engaged in planning, designing, building, validating and maintaining modern cGMP pharmaceutical manufacturing facilities in the U.S. and internationally. The new edition expands on facility planning, with a focus on the ever-growing need to modify existing legacy facilities, and on current trends in pharmaceutical manufacturing which include strategies for sustainability and LEED building ratings. All chapters have been re-examined with a fresh outlook on current good design practices.
Book Synopsis Pharmaceutical Facilities by : Manohar A Potdar
Download or read book Pharmaceutical Facilities written by Manohar A Potdar and published by . This book was released on 2014-11 with total page 306 pages. Available in PDF, EPUB and Kindle. Book excerpt: Designing, erection and commissioning of a pharmaceutical plant is a long drawn process. It needs basic understanding of pharmaceutical formulations and their logical and sequential processing. This whole process is tedious, time consuming and should have proper guidance in this regard. The book will provide such guidance which is a long felt need by the industry. Salient Features: - Pharmaceutical design aspects with sample layouts for all major formulations are discussed - All aspects related to project management, regulatory requirements, validation of facilities, HVAC and water system are discussed - A real handy book for all those who are involved in plant design, project management and facility and utilities validation in Pharmaceutical industry.
Book Synopsis Facility Piping Systems Handbook by : Michael L. Frankel
Download or read book Facility Piping Systems Handbook written by Michael L. Frankel and published by McGraw Hill Professional. This book was released on 2009-09-02 with total page 1040 pages. Available in PDF, EPUB and Kindle. Book excerpt: A Comprehensive Guide to Facility Piping Systems Fully up-to-date with the latest codes and standards, this practical resource contains everything you need to plan, select, design, specify, and test piping systems for industry, commercial, and institutional applications. The book includes complete coverage of pipes, fittings, valves, jointing methods, hangers, supports, pumps, tanks, and other required equipment. Facility Piping Systems Handbook, Third Edition, progresses from fundamentals of systems operation to a design procedure that allows quick and accurate component and pipe sizing. Listings of FDA, EPA, and OSHA requirements are included. Complete with formulas, charts, and tables, this invaluable all-in-one volume will save you time and money on the job. Coverage includes: Water treatment and purification Heat transfer, insulation, and freeze protection Cryogenic storage Facility steam and condensate systems Liquid fuel storage and dispensing Fuel gas and compressed gas systems Vacuum air systems Animal facility piping systems Life safety systems Nonpotable and drinking water systems Swimming pools, spas, and water attractions And more
Book Synopsis Facility Piping Systems Handbook by : Michael Frankel
Download or read book Facility Piping Systems Handbook written by Michael Frankel and published by McGraw-Hill Companies. This book was released on 1996 with total page 1046 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Book Synopsis Process Architecture in Biomanufacturing Facility Design by : Jeffery Odum
Download or read book Process Architecture in Biomanufacturing Facility Design written by Jeffery Odum and published by John Wiley & Sons. This book was released on 2018-01-26 with total page 381 pages. Available in PDF, EPUB and Kindle. Book excerpt: Essential information for architects, designers, engineers, equipment suppliers, and other professionals who are working in or entering the biopharmaceutical manufacturing field Biomanufacturing facilities that are designed and built today are radically different than in the past. The vital information and knowledge needed to design and construct these increasingly sophisticated biopharmaceutical manufacturing facilities is difficult to find in published literature—and it’s rarely taught in architecture or design schools. This is the first book for architects and designers that fills this void. Process Architecture in Biomanufacturing Facility Design provides information on design principles of biopharmaceutical manufacturing facilities that support emerging innovative processes and technologies, use state-of-the-art equipment, are energy efficient and sustainable, and meet regulatory requirements. Relying on their many years of hands-on design and operations experience, the authors emphasize concepts and practical approaches toward design, construction, and operation of biomanufacturing facilities, including product-process-facility relationships, closed systems and single use equipment, aseptic manufacturing considerations, design of biocontainment facility and process based laboratory, and sustainability considerations, as well as an outlook on the facility of the future. Provides guidelines for meeting licensing and regulatory requirements for biomanufacturing facilities in the U.S.A and WHO—especially in emerging global markets in India, China, Latin America, and the Asia/Pacific regions Focuses on innovative design and equipment, to speed construction and time to market, increase energy efficiency, and reduce footprint, construction and operational costs, as well as the financial risks associated with construction of a new facility prior to the approval of the manufactured products by regulatory agencies Includes many diagrams that clarify the design approach Process Architecture in Biomanufacturing Facility Design is an ideal text for professionals involved in the design of facilities for manufacturing of biopharmaceuticals and vaccines, biotechnology, and life-science industry, including architects and designers of industrial facilities, construction, equipment vendors, and mechanical engineers. It is also recommended for university instructors, advanced undergraduates, and graduate students in architecture, industrial engineering, mechanical engineering, industrial design, and industrial interior design.
Book Synopsis International Plumbing Code by : International Code Council
Download or read book International Plumbing Code written by International Code Council and published by . This book was released on 2014-06-05 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt: With an emphasis on design and installation for optimum performance, the 2015 INTERNATIONAL PLUMBING CODE SOFT COVER sets forth established requirements for plumbing systems. This important reference guide includes provisions for fixtures, piping, fittings, and devices, as well as design and installation methods for water supply, sanitary drainage, and storm drainage. The 2015 edition of the code includes information on public toilet facilities, as well as water temperature limiting devices, and replacement water heater installation. Using both prescriptive- and performance-related specifications, this code provides comprehensive minimum regulations for a variety of plumbing facilities, facilitating the design and acceptance of new and innovative products, materials, and systems.
Book Synopsis A Guide to Piping Design and Engineering by : Anuj Bhatia
Download or read book A Guide to Piping Design and Engineering written by Anuj Bhatia and published by . This book was released on 2016-03-12 with total page 822 pages. Available in PDF, EPUB and Kindle. Book excerpt: One of the most important components of the infrastructure is the vast network of pipelines and process piping-literally millions and millions of miles. The term "pipelines" generally refers to the network of pipelines that transport water, sewage, steam, and gaseous and liquid hydrocarbons from sources (e.g., reservoirs, steam plants, oil and gas wells, refineries) to local distribution centers ("transmission pipelines"), and to the network of pipelines that distribute such products to local markets and end users ("distribution" pipelines). The term "process piping" generally refers to the system of pipes that transport process fluids (e.g. industrial gases, fuels, chemicals etc.) around an industrial facility involved in the manufacture of products or in the generation of power. It also is used to describe utility piping systems (e.g., air, steam, water, compressed air, fuels etc.) that are used in, or in support of the industrial process. Also, certain drainage piping--where corrosive or toxic fluids are being transported and severe conditions may be present, or where it is simply outside the scope of plumbing codes--is also sometimes classified as process piping. Some places where process piping is used are obvious, such as chemical and petrochemical plants, petroleum refineries, pharmaceutical manufacturing facilities and pulp & paper plants. However, there are many other not so obvious places where process piping is commonplace, such as semiconductor facilities, automotive and aircraft plants, water treatment operations, waste treatment facilities and many others.This book comprises of 9 course modules, which cover all aspects of piping design in easy to learn format. All topics are introduced to readers with no or limited background on the subject. A multiple choice quiz (total 255 questions) is provided at the end of each module to test the readers' knowledge and enhance learning. The book is very comprehensive and refresher to engineers and designers working in the field of piping in Oil and Gas, Chemical and Industrial plants. It is also very useful to fresh engineers joining industries for improving their knowledge in the field of fluid transportation and pipework.
Book Synopsis Drinking Water Distribution Systems by : National Research Council
Download or read book Drinking Water Distribution Systems written by National Research Council and published by National Academies Press. This book was released on 2006-12-22 with total page 404 pages. Available in PDF, EPUB and Kindle. Book excerpt: Protecting and maintaining water distributions systems is crucial to ensuring high quality drinking water. Distribution systems-consisting of pipes, pumps, valves, storage tanks, reservoirs, meters, fittings, and other hydraulic appurtenances-carry drinking water from a centralized treatment plant or well supplies to consumers' taps. Spanning almost 1 million miles in the United States, distribution systems represent the vast majority of physical infrastructure for water supplies, and thus constitute the primary management challenge from both an operational and public health standpoint. Recent data on waterborne disease outbreaks suggest that distribution systems remain a source of contamination that has yet to be fully addressed. This report evaluates approaches for risk characterization and recent data, and it identifies a variety of strategies that could be considered to reduce the risks posed by water-quality deteriorating events in distribution systems. Particular attention is given to backflow events via cross connections, the potential for contamination of the distribution system during construction and repair activities, maintenance of storage facilities, and the role of premise plumbing in public health risk. The report also identifies advances in detection, monitoring and modeling, analytical methods, and research and development opportunities that will enable the water supply industry to further reduce risks associated with drinking water distribution systems.
Book Synopsis An Introduction to Plumbing and Gas Systems for Medical Facilities by : J. Guyer
Download or read book An Introduction to Plumbing and Gas Systems for Medical Facilities written by J. Guyer and published by Createspace Independent Publishing Platform. This book was released on 2014-04-14 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt: This publication provides an introduction to the design of plumbing and gas systems for medical and dental treatment facilities including hospitals and clinics.
Book Synopsis Facilities Site Piping Systems Handbook by : Michael Frankel
Download or read book Facilities Site Piping Systems Handbook written by Michael Frankel and published by McGraw Hill Professional. This book was released on 2012-08-29 with total page 514 pages. Available in PDF, EPUB and Kindle. Book excerpt: "Featuring the latest codes and standards, this detailed resource discusses the design of facility piping systems that are installed on the site beyond the building wall. This is a comprehensive guide to the identification, measurement, transport, and disposal of various kinds of waterborne waste as well as to the supply of water and natural gas to facilities. Water conservation and reuse are also addressed"--P. [4] of cover.
Book Synopsis Plumbing Engineering Design Handbook, Volume 1 by : American Society of Plumbing Engineers
Download or read book Plumbing Engineering Design Handbook, Volume 1 written by American Society of Plumbing Engineers and published by . This book was released on 2017 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:
Book Synopsis Handbook of Pharmaceutical Manufacturing Formulations, Third Edition by : Sarfaraz K. Niazi
Download or read book Handbook of Pharmaceutical Manufacturing Formulations, Third Edition written by Sarfaraz K. Niazi and published by CRC Press. This book was released on 2019-11-25 with total page 457 pages. Available in PDF, EPUB and Kindle. Book excerpt: The Handbook of Pharmaceutical Manufacturing Formulations, Third Edition: Volume Two, Uncompressed Solid Products is an authoritative and practical guide to the art and science of formulating drugs for commercial manufacturing. With thoroughly revised and expanded content, this second volume of a six-volume set, compiles data from FDA and EMA new drug applications, patents and patent applications, and other sources of generic and proprietary formulations including author’s own experience, to cover the broad spectrum of cGMP formulations and issues in using these formulations in a commercial setting. A must-have collection for pharmaceutical manufacturers, educational institutions, and regulatory authorities, this is an excellent platform for drug companies to benchmark their products and for generic companies to formulate drugs coming off patent. Features: Largest source of authoritative and practical formulations, cGMP compliance guidance and self-audit suggestions Differs from other publications on formulation science in that it focuses on readily scalable commercial formulations that can be adopted for cGMP manufacturing Tackles common difficulties in formulating drugs and presents details on stability testing, bioequivalence testing, and full compliance with drug product safety elements Written by a well-recognized authority on drug and dosage form development including biological drugs and alternative medicines
Book Synopsis How to Validate a Pharmaceutical Process by : Steven Ostrove
Download or read book How to Validate a Pharmaceutical Process written by Steven Ostrove and published by Academic Press. This book was released on 2016-06-07 with total page 219 pages. Available in PDF, EPUB and Kindle. Book excerpt: How to Validate a Pharmaceutical Process provides a "how to approach to developing and implementing a sustainable pharmaceutical process validation program. The latest volume in the Expertise in Pharmaceutical Process Technology Series, this book illustrates the methods and reasoning behind processes and protocols. It also addresses practical problems and offers solutions to qualify and validate a pharmaceutical process. Understanding the "why is critical to a successful and defensible process validation, making this book an essential research companion for all practitioners engaged in pharmaceutical process validation. - Thoroughly referenced and based on the latest research and literature - Illustrates the most common issues related to developing and implementing a sustainable process validation program and provides examples on how to be successful - Covers important topics such as the lifecycle approach, quality by design, risk assessment, critical process parameters, US and international regulatory guidelines, and more
Book Synopsis The Certified Pharmaceutical GMP Professional Handbook by : Mark Allen Durivage
Download or read book The Certified Pharmaceutical GMP Professional Handbook written by Mark Allen Durivage and published by Quality Press. This book was released on 2016-05-23 with total page 404 pages. Available in PDF, EPUB and Kindle. Book excerpt: 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.
Book Synopsis Good Manufacturing Practice in Transfusion Medicine by : C.Th. Smit Sibinga
Download or read book Good Manufacturing Practice in Transfusion Medicine written by C.Th. Smit Sibinga and published by Springer Science & Business Media. This book was released on 2012-12-06 with total page 293 pages. Available in PDF, EPUB and Kindle. Book excerpt: TQM AND TAYLORISM; HOW THEY COMPARE H. Bremer Preface The industrial world today is divided between two camps: a culture based on the principles of Total Quality Management (TQM), developed in the Far East, and one still strongly influenced by the origins of "Scientific Management", intro duced in the West by F.W. Taylor and others at the turn of the century. This divergence will be shown to have arisen in the last forty years, long enough for a new generation of managers and corresponding culture to emerge. The two cul tures are so deeply entrenched that it is difficult for one to change to the other. However, there is strong evidence to support the contention that people-oriented TQM is superior, and those companies clinging to Taylor models now face diffi cult decisions. Actions by Taylor-companies to move to TQM rnight weH be hindered rather than helped by applying present Quality Assurance Standards, developed by Taylor-oriented national and international Standards Institutions.