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Sterile Processing of Pharmaceutical Products Sterile Processing of Pharmaceutical Products Engineering Practice, Validation, and Compliance in Regulated Environments Sam A. Hout Mission Viejo CA, USA This edition irst published 2022 © 2022 John Wiley Sons, Inc. All rights reserved. No part of this publication may be reproduced, stored in a retrieval system, or transmitted, in any form or by any means, electronic, mechanical, photocopying, recording or otherwise, except as permitted by law. Advice on how to obtain permission to reuse material from this title is available at /go/permissions. The right of Sam A. Hout to be identiied as the author of this work has been asserted in accordance with law. Registered Oice John Wiley Sons, Inc., 111 River Street, Hoboken, NJ 07030, USA Editorial Oice 111 River Street, Hoboken, NJ 07030, USA For details of our global editorial oices, customer services, and more information about Wiley products visit us at . Wiley also publishes its books in a variety of electronic formats and by print-on-demand. Some content that appears in standard print versions of this book may not be available in other formats. Limit of Liability/Disclaimer of Warranty While the publisher and authors have used their best eforts in preparing this work, they make no representations or warranties with respect to the accuracy or completeness of the contents of this work and speciically disclaim all warranties, including without limitation any implied warranties of merchantability or itness for a particular purpose. No warranty may be created or extended by sales representatives, written sales materials or promotional statements for this work. The fact that an organization, website, or product is referred to in this work as a citation and/or potential source of further information does not mean that the publisher and authors endorse the information or services the organization, website, or product may provide or recommendat