ISPE Baseline Pharmaceutical Engineering Guide for New and Renovated Facilities

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Publisher :
ISBN 13 : 9781936379644
Total Pages : 136 pages
Book Rating : 4.3/5 (796 download)

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Book Synopsis ISPE Baseline Pharmaceutical Engineering Guide for New and Renovated Facilities by :

Download or read book ISPE Baseline Pharmaceutical Engineering Guide for New and Renovated Facilities written by and published by . This book was released on 2013 with total page 136 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Pharmaceutical Engineering Guides for New and Renovated Facilities

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Publisher :
ISBN 13 : 9781931879095
Total Pages : 190 pages
Book Rating : 4.8/5 (79 download)

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Book Synopsis Pharmaceutical Engineering Guides for New and Renovated Facilities by : ISPE

Download or read book Pharmaceutical Engineering Guides for New and Renovated Facilities written by ISPE and published by . This book was released on 2004-06-01 with total page 190 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Sterile Product Manufacturing Facilities

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Publisher :
ISBN 13 : 9781936379149
Total Pages : 200 pages
Book Rating : 4.3/5 (791 download)

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Book Synopsis Sterile Product Manufacturing Facilities by : International Society for Pharmaceutical Engineering

Download or read book Sterile Product Manufacturing Facilities written by International Society for Pharmaceutical Engineering and published by . This book was released on 2011 with total page 200 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Pharmaceutical Engineering Guides for New and Renovated Facilities

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Publisher :
ISBN 13 : 9781931879095
Total Pages : 0 pages
Book Rating : 4.8/5 (79 download)

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Book Synopsis Pharmaceutical Engineering Guides for New and Renovated Facilities by :

Download or read book Pharmaceutical Engineering Guides for New and Renovated Facilities written by and published by . This book was released on 1996 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Biopharmaceutical Manufacturing Facilities

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Publisher :
ISBN 13 :
Total Pages : 190 pages
Book Rating : 4.:/5 (229 download)

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Book Synopsis Biopharmaceutical Manufacturing Facilities by : International Society of Pharmaceutical Engineers

Download or read book Biopharmaceutical Manufacturing Facilities written by International Society of Pharmaceutical Engineers and published by . This book was released on 2004 with total page 190 pages. Available in PDF, EPUB and Kindle. Book excerpt:

ISPE Baseline® Guide: Volume 3 - Sterile Product Manufacturing Facilities

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Publisher :
ISBN 13 : 9781936379170
Total Pages : pages
Book Rating : 4.3/5 (791 download)

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Book Synopsis ISPE Baseline® Guide: Volume 3 - Sterile Product Manufacturing Facilities by : Ispe

Download or read book ISPE Baseline® Guide: Volume 3 - Sterile Product Manufacturing Facilities written by Ispe and published by . This book was released on 2011-10-25 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:

Baseline Pharmaceutical Engineering Guide: Sterile manufacturing facilities

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Publisher :
ISBN 13 :
Total Pages : pages
Book Rating : 4.:/5 (382 download)

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Book Synopsis Baseline Pharmaceutical Engineering Guide: Sterile manufacturing facilities by :

Download or read book Baseline Pharmaceutical Engineering Guide: Sterile manufacturing facilities written by and published by . This book was released on 1996 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:

Biopharmaceutical Manufacturing

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Author :
Publisher : Walter de Gruyter GmbH & Co KG
ISBN 13 : 3110617013
Total Pages : 433 pages
Book Rating : 4.1/5 (16 download)

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Book Synopsis Biopharmaceutical Manufacturing by : Gary Gilleskie

Download or read book Biopharmaceutical Manufacturing written by Gary Gilleskie and published by Walter de Gruyter GmbH & Co KG. This book was released on 2021-09-07 with total page 433 pages. Available in PDF, EPUB and Kindle. Book excerpt: Biopharmaceuticals, medicines made by or from living organisms (including cells from living organisms), are extremely effective in treating a broad range of diseases. Their importance to human health has grown significantly over the years as more biopharmaceutical products have entered the market, and now the biggest selling drugs in the world are biopharmaceuticals. Biopharmaceutical Manufacturing: Principles, Processes and Practices provides concise, comprehensive, and up-to-date coverage of biopharmaceutical manufacturing. Written in a clear and informal style, the content has been influenced by the authors’ substantial industry experience and teaching expertise. That expertise enables the authors to address the many questions posed over the years both by university students and professionals with experience in the field. Consequently, the book will appeal both to undergraduate or graduate students using it as a textbook and specialized industry practitioners seeking to understand the big picture of biopharmaceutical manufacturing. This book:

Baseline Pharmaceutical Engineering Guide

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Publisher :
ISBN 13 :
Total Pages : 100 pages
Book Rating : 4.:/5 (41 download)

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Book Synopsis Baseline Pharmaceutical Engineering Guide by :

Download or read book Baseline Pharmaceutical Engineering Guide written by and published by . This book was released on 1999 with total page 100 pages. Available in PDF, EPUB and Kindle. Book excerpt:

Process Architecture in Biomanufacturing Facility Design

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Publisher : John Wiley & Sons
ISBN 13 : 1118833651
Total Pages : 381 pages
Book Rating : 4.1/5 (188 download)

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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.

Process Validation in Manufacturing of Biopharmaceuticals

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Publisher : CRC Press
ISBN 13 : 1003805469
Total Pages : 413 pages
Book Rating : 4.0/5 (38 download)

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Book Synopsis Process Validation in Manufacturing of Biopharmaceuticals by : Anurag Singh Rathore

Download or read book Process Validation in Manufacturing of Biopharmaceuticals written by Anurag Singh Rathore and published by CRC Press. This book was released on 2023-12-18 with total page 413 pages. Available in PDF, EPUB and Kindle. Book excerpt: The fourth edition of Process Validation in Manufacturing of Biopharmaceuticals is a practical and comprehensive resource illustrating the different approaches for successful validation of biopharmaceutical processes. A pivotal text in its field, this new edition provides guidelines and current practices, contains industrial case studies, and is expanded to include in-depth analysis of the new Process Validation (PV) guidance from the US FDA. Key Features: Offers readers a thorough understanding of the key concepts that form the basis of a good process validation program for biopharmaceuticals. Includes case studies from the various industry leaders that demonstrate application of these concepts. Discusses the use of modern tools such as multivariate analysis for facilitating a process validation exercise. Covers process characterization techniques for scaling down unit operations in biopharmaceutical manufacturing, including chromatography, chemical modification reactions, ultrafiltration, and microfiltration, and practical methods to test raw materials and in-process samples. Providing a thorough understanding of the key concepts that form the basis of a good process validation program, this book will help readers ensure that PV is carried out and exceeds expectations. Fully illustrated, this is a much-needed practical guide for biopharmaceutical manufacturers.

Risk-based Manufacture of Pharmaceutical Products

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Publisher :
ISBN 13 : 9781931879965
Total Pages : 148 pages
Book Rating : 4.8/5 (799 download)

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Book Synopsis Risk-based Manufacture of Pharmaceutical Products by : International Society for Pharmaceutical Engineering

Download or read book Risk-based Manufacture of Pharmaceutical Products written by International Society for Pharmaceutical Engineering and published by . This book was released on 2010 with total page 148 pages. Available in PDF, EPUB and Kindle. Book excerpt:

ISPE Baseline® Guide: Volume 1 - Active Pharmaceutical Ingredients

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Publisher :
ISBN 13 : 9781931879590
Total Pages : pages
Book Rating : 4.8/5 (795 download)

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Book Synopsis ISPE Baseline® Guide: Volume 1 - Active Pharmaceutical Ingredients by : Ispe

Download or read book ISPE Baseline® Guide: Volume 1 - Active Pharmaceutical Ingredients written by Ispe and published by . This book was released on 2008-04-17 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:

ISPE Baseline® Guide: Volume 7 - Risk-Based Manufacture of Pharmaceutical Products (Risk-MaPP)

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Publisher :
ISBN 13 : 9781936379026
Total Pages : pages
Book Rating : 4.3/5 (79 download)

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Book Synopsis ISPE Baseline® Guide: Volume 7 - Risk-Based Manufacture of Pharmaceutical Products (Risk-MaPP) by : Ispe

Download or read book ISPE Baseline® Guide: Volume 7 - Risk-Based Manufacture of Pharmaceutical Products (Risk-MaPP) written by Ispe and published by . This book was released on 2011-04-15 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:

Biopharmaceutical Processing

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Publisher : Elsevier
ISBN 13 : 0128125527
Total Pages : 1308 pages
Book Rating : 4.1/5 (281 download)

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Book Synopsis Biopharmaceutical Processing by : Gunter Jagschies

Download or read book Biopharmaceutical Processing written by Gunter Jagschies and published by Elsevier. This book was released on 2018-01-18 with total page 1308 pages. Available in PDF, EPUB and Kindle. Book excerpt: Biopharmaceutical Processing: Development, Design, and Implementation of Manufacturing Processes covers bioprocessing from cell line development to bulk drug substances. The methods and strategies described are essential learning for every scientist, engineer or manager in the biopharmaceutical and vaccines industry. The integrity of the bioprocess ultimately determines the quality of the product in the biotherapeutics arena, and this book covers every stage including all technologies related to downstream purification and upstream processing fields. Economic considerations are included throughout, with recommendations for lowering costs and improving efficiencies. Designed for quick reference and easy accessibility of facts, calculations and guidelines, this book is an essential tool for industrial scientists and managers in the biopharmaceutical industry. Offers a comprehensive, go-to reference for daily work decisions Covers both upstream and downstream processes Includes case studies that emphasize financial outcomes Presents summaries, decision grids, graphs and overviews for quick reference

Handbook for Critical Cleaning: Applications, processes, and controls

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Publisher : CRC Press
ISBN 13 : 1439828296
Total Pages : 576 pages
Book Rating : 4.4/5 (398 download)

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Book Synopsis Handbook for Critical Cleaning: Applications, processes, and controls by : Barbara Kanegsberg

Download or read book Handbook for Critical Cleaning: Applications, processes, and controls written by Barbara Kanegsberg and published by CRC Press. This book was released on 2011 with total page 576 pages. Available in PDF, EPUB and Kindle. Book excerpt: "Nearly all companies which manufacture or fabricate high-value physical objects (components, parts, assemblies) perform critical cleaning at one or more stages. These range from the giants of the semiconductor, aerospace, and biomedical world to a host of small to medium to large companies producing a dizzying array of components"--

Handbook of Validation in Pharmaceutical Processes, Fourth Edition

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Publisher : CRC Press
ISBN 13 : 1000436012
Total Pages : 1062 pages
Book Rating : 4.0/5 (4 download)

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Book Synopsis Handbook of Validation in Pharmaceutical Processes, Fourth Edition by : James Agalloco

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