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Condition: New. Brand New. Soft Cover International Edition. Different ISBN and Cover Image. Priced lower than the standard editions which is usually intended to make them more affordable for students abroad. The core content of the book is generally the same as the standard edition. The country selling restrictions may be printed on the book but is no problem for the self-use. This Item maybe shipped from US or any other country as we have multiple locations worldwide.
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Seller: Greenworld Books, Arlington, TX, U.S.A.
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Couverture souple. Condition: Très bon. Pas de jaquette. 2004 Occasion 294 Pages 460 Grammes.
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Broché. Condition: D'occasion - Bon état. Dédicace manuscrite de l'auteur. L'Harmattan, 2003. Coins légèrement cornés, livre en très bon état général sinon. Envoi rapide et soigné.
Seller: Revaluation Books, Exeter, United Kingdom
Paperback. Condition: Brand New. 296 pages. French language. 9.21x6.30x0.79 inches. In Stock.
Condition: Good. Envoi rapide Bon Etat. in8. 2004. Broché. 266 pages. envoi de l'auteur en page de garde. Good.
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Seller: Brook Bookstore On Demand, Napoli, NA, Italy
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HRD. Condition: New. New Book. Shipped from UK. Established seller since 2000.
Seller: Ria Christie Collections, Uxbridge, United Kingdom
£ 132.32
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paperback. Condition: Very Good. Softcover. Clean text - NO writing, NO highlighting. 3 pages toward the end of the book are creased at fore-edge head corner. Very good- reading copy.
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Taschenbuch. Condition: Neu. Pharmaceutical Stability Testing to Support Global Markets | Kim Huynh-Ba | Taschenbuch | xx | Englisch | 2012 | Humana | EAN 9781461425366 | Verantwortliche Person für die EU: Springer Verlag GmbH, Tiergartenstr. 17, 69121 Heidelberg, juergen[dot]hartmann[at]springer[dot]com | Anbieter: preigu.
Language: English
Published by John Wiley & Sons Inc, New York, 2022
ISBN 10: 1119120918 ISBN 13: 9781119120919
Seller: CitiRetail, Stevenage, United Kingdom
Hardcover. Condition: new. Hardcover. Provides practical guidance on pharmaceutical analysis, written by leading experts with extensive industry experience Analytical Testing for the Pharmaceutical GMP Laboratory presents a thorough overview of the pharmaceutical regulations, working processes, and drug development best practices used to maintain the quality and integrity of medicines. With a focus on smaller molecular weight drug substances and products, the book provides the knowledge necessary for establishing the pharmaceutical laboratory to support Quality Systems while maintaining compliance with Good Manufacturing Practices (GMP) regulations. Concise yet comprehensive chapters contain up-to-date coverage of drug regulations, pharmaceutical analysis methodologies, control strategies, testing development and validation, method transfer, electronic data documentation, and more. Each chapter includes a table of contents, definitions of acronyms, a reference list, and ample tables and figures. Addressing the principal activities and regulatory challenges of analytical testing in the development and manufacturing of pharmaceutical drug products, this authoritative resource: Describes the structure, roles, core guidelines, and GMP regulations of the FDA and ICH.Covers the common analytical technologies used in pharmaceutical laboratories, including examples of analytical techniques used for the release and stability testing of drugs.Examines control strategies established from quality systems supported by real-world case studies.Explains the use of dissolution testing for products such as extended-release capsules, aerosols, and inhalers.Discusses good documentation and data reporting practices, stability programs, and the Laboratory Information Management System (LIMS) to maintain compliance.Includes calculations, application examples, and illustrations to assist readers in day-to-day laboratory operations.Contains practical information and templates to structure internal processes or common Standard Operating Procedures (SOPs). Analytical Testing for the Pharmaceutical GMP Laboratory is a must-have reference for both early-career and experienced pharmaceutical scientists, analytical chemists, pharmacists, and quality control professionals. It is also both a resource for GMP laboratory training programs and an excellent textbook for undergraduate and graduate courses of analytical chemistry in pharmaceutical sciences or regulatory compliance programs. Shipping may be from our UK warehouse or from our Australian or US warehouses, depending on stock availability.
Language: English
Published by John Wiley & Sons Inc, 2022
ISBN 10: 1119120918 ISBN 13: 9781119120919
Seller: Kennys Bookshop and Art Galleries Ltd., Galway, GY, Ireland
First Edition
Condition: New. 2022. 1st Edition. Hardcover. . . . . .
Condition: New.