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Author : British Standards Institution
Publisher :
ISBN 13 :
Total Pages : 60 pages
Book Rating : 4.:/5 (515 download)
Download or read book Cleanrooms and Associated Controlled Environments written by British Standards Institution and published by . This book was released on 1997 with total page 60 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Author : International Organization for Standardization
Publisher :
ISBN 13 :
Total Pages : pages
Book Rating : 4.:/5 (595 download)
Download or read book Cleanrooms and Associated Controlled Environments written by International Organization for Standardization and published by . This book was released on 1997 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:
Author : British Standards Institute Staff
Publisher :
ISBN 13 : 9780580379857
Total Pages : 64 pages
Book Rating : 4.3/5 (798 download)
Download or read book Cleanrooms and Associated Controlled Environments. Design, Construction and Start-Up written by British Standards Institute Staff and published by . This book was released on 2001-07-15 with total page 64 pages. Available in PDF, EPUB and Kindle. Book excerpt: Clean rooms, Environmental cleanliness, Air cleaning equipment, Environment (working), Controlled-atmosphere rooms, Design, Performance, Construction
Author : Polska. Polski Komitet Normalizacyjny
Publisher :
ISBN 13 : 9788323685555
Total Pages : 54 pages
Book Rating : 4.6/5 (855 download)
Download or read book Cleanrooms and Associated Controlled Environments - Part 4: Design, Construction and Start-up (ISO 14644-4:2001) written by Polska. Polski Komitet Normalizacyjny and published by . This book was released on 2002 with total page 54 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book Cleanrooms and associated controlled environments. Part 4, Design, construction and start-up (ISO/DIS 14644-4:2021) written by and published by . This book was released on 2021 with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:
Author : Standards South Africa
Publisher :
ISBN 13 : 9780626147587
Total Pages : 51 pages
Book Rating : 4.1/5 (475 download)
Download or read book Cleanrooms and Associated Controlled Environments written by Standards South Africa and published by . This book was released on 2003 with total page 51 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Author : Standards Australia (Organization)
Publisher :
ISBN 13 :
Total Pages : 52 pages
Book Rating : 4.:/5 (18 download)
Download or read book Cleanrooms and Associated Controlled Environments written by Standards Australia (Organization) and published by . This book was released on 2006 with total page 52 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Author : Standards Australia International Limited
Publisher :
ISBN 13 : 9780733746116
Total Pages : 51 pages
Book Rating : 4.7/5 (461 download)
Download or read book Cleanrooms and Associated Controlled Environments, Part 4 written by Standards Australia International Limited and published by . This book was released on 2002 with total page 51 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Author : British Standards Institution
Publisher :
ISBN 13 :
Total Pages : 0 pages
Book Rating : 4.:/5 (137 download)
Download or read book Tracked Changes. Cleanrooms and Associated Controlled Environments written by British Standards Institution and published by . This book was released on 2023 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Author : International Organization for Standardization
Publisher :
ISBN 13 :
Total Pages : 0 pages
Book Rating : 4.:/5 (14 download)
Download or read book Cleanrooms and Associated Controlled Environments. Part 4. Design and Construction written by International Organization for Standardization and published by . This book was released on 2001 with total page 0 pages. Available in PDF, EPUB and Kindle. Book excerpt:
Download or read book AS/NZS ISO 14644.4 written by and published by . This book was released on with total page pages. Available in PDF, EPUB and Kindle. Book excerpt:
Author : Mark Allen Durivage
Publisher : Quality Press
ISBN 13 : 0873899334
Total Pages : 386 pages
Book Rating : 4.8/5 (738 download)
Download or read book The Certified Pharmaceutical GMP Professional Handbook, Second Edition written by Mark Allen Durivage and published by Quality Press. This book was released on 2016-05-26 with total page 386 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.
Author : Mark Allen Durivage
Publisher : Quality Press
ISBN 13 : 1636941516
Total Pages : 421 pages
Book Rating : 4.6/5 (369 download)
Download or read book The ASQ Certified Pharmaceutical GMP Professional Handbook written by Mark Allen Durivage and published by Quality Press. This book was released on 2024-09-30 with total page 421 pages. Available in PDF, EPUB and Kindle. Book excerpt: The ASQ Certified Pharmaceutical GMP Professional Handbook assists candidates preparing for the Certified Pharmaceutical Good Manufacturing Practices Professional (CPGP) examination and serves as a handy reference guide for practitioners in the field. This handbook covers compliance with good manufacturing practices (GMPs) as regulated and guided by national and international agencies for the pharmaceutical industry.
Author : Sarfaraz K. Niazi
Publisher : CRC Press
ISBN 13 : 135159222X
Total Pages : 513 pages
Book Rating : 4.3/5 (515 download)
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 2019-12-09 with total page 513 pages. Available in PDF, EPUB and Kindle. Book excerpt: The Handbook of Pharmaceutical Manufacturing Formulations, Third Edition: Volume Six, Sterile 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 sixth 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
Author : James T. Walker
Publisher : Woodhead Publishing
ISBN 13 : 0081025661
Total Pages : 594 pages
Book Rating : 4.0/5 (81 download)
Download or read book Decontamination in Hospitals and Healthcare written by James T. Walker and published by Woodhead Publishing. This book was released on 2019-11-26 with total page 594 pages. Available in PDF, EPUB and Kindle. Book excerpt: Decontamination in Hospitals and Healthcare, Second Edition, enables users to obtain detailed knowledge of decontamination practices in healthcare settings, including surfaces, devices, clothing and people, with a specific focus on hospitals and dental clinics. - Offers in-depth coverage of all aspects of decontamination in healthcare - Examines the decontamination of surgical equipment and endoscopes - Expanded to include new information on behavioral principles in decontamination, control of microbiological problems, waterborne microorganisms, pseudomonas and the decontamination of laundry
Author : Lucia Clontz
Publisher : CRC Press
ISBN 13 : 1420053493
Total Pages : 344 pages
Book Rating : 4.4/5 (2 download)
Download or read book Microbial Limit and Bioburden Tests written by Lucia Clontz and published by CRC Press. This book was released on 2008-10-14 with total page 344 pages. Available in PDF, EPUB and Kindle. Book excerpt: In recent years, the field of pharmaceutical microbiology has experienced numerous technological advances, accompanied by the publication of new and harmonized compendial methods. It is therefore imperative for those who are responsible for monitoring the microbial quality of pharmaceutical/biopharmaceutical products to keep abreast of the latest c
Author : Kathleen E. McCormick
Publisher : Butterworth-Heinemann
ISBN 13 : 0323994601
Total Pages : 385 pages
Book Rating : 4.3/5 (239 download)
Download or read book Quality written by Kathleen E. McCormick and published by Butterworth-Heinemann. This book was released on 2022-07-14 with total page 385 pages. Available in PDF, EPUB and Kindle. Book excerpt: Quality, second edition, provides comprehensive application of regulatory guidelines and quality concepts and methodologies related to pharmaceutical manufacturing. It is an excellent resource for practitioners, those pursuing pharmaceutical related certifications, and for students trying to learn more about pharmaceutical manufacturing. This book provides the background theory, applied descriptions of the guidelines and concepts, plus questions and problems at the end of the chapters that will help provide practice for the reader to apply the concepts. In this book the authors share their combined 60+ years of extensive practical experience in the industry and in process improvement combined with detailed understanding of the needs of the industry and education system. This book provides real-life examples from industry and guidelines for practical application of tools that can be referenced by operators, engineers, and management.This book is fully revised, updated, and expanded with new content in areas such as QbD, Lean, Six Sigma, basic data analysis, and CAPA tools. - Fully revised, updated, and expanded new edition - Features new topics such as QbD, Lean, Six Sigma, basic data analysis, and CAPA tools - Includes end-of-chapter summaries and end-of-chapter question and/or problems - Provides detailed steps and examples for applying the guidelines and quality tools - Written in an accessible style making the content easy to understand and apply
