Vendeur : Books Puddle, New York, NY, Etats-Unis
EUR 81,68
Quantité disponible : 4 disponible(s)
Ajouter au panierEtat : New. pp. 375 1st Edition.
Vendeur : THE SAINT BOOKSTORE, Southport, Royaume-Uni
EUR 79,68
Quantité disponible : 1 disponible(s)
Ajouter au panierHardback. Etat : New. New copy - Usually dispatched within 4 working days.
EUR 69,04
Quantité disponible : Plus de 20 disponibles
Ajouter au panierGebunden. Etat : New. Phil CloudAll current Good Manufacturing Practices (cGMP), Good Clinical Practices (GCP), Good Laboratory Practices (GLP) and ISO 9000 standards and regulations require that validation document be established and followed. Yet these regulations do no.
Langue: anglais
Edité par Noyes Publications 1999-10-01, 1999
ISBN 10 : 0815514107 ISBN 13 : 9780815514107
Vendeur : Chiron Media, Wallingford, Royaume-Uni
EUR 107,25
Quantité disponible : 1 disponible(s)
Ajouter au panierHardcover. Etat : New.
EUR 126,07
Quantité disponible : 1 disponible(s)
Ajouter au panierhardcover. Etat : New. In shrink wrap. Looks like an interesting title!
Langue: anglais
Edité par Taylor & Francis Inc Aug 1999, 1999
ISBN 10 : 1574910981 ISBN 13 : 9781574910988
Vendeur : AHA-BUCH GmbH, Einbeck, Allemagne
EUR 87,34
Quantité disponible : 2 disponible(s)
Ajouter au panierBuch. Etat : Neu. Neuware - Focusing specifically on the FDA documentation requirements, How to Develop and Manage Qualification Protocols for FDA Compliance provides readers with concrete guidance on how to develop and manage qualification protocols and their associated documentation to ensure that their companies are not at risk. It discusses key function areas, such as cleaning, facilities and utilities, equipment, computers and software, and process in detail. The book contains 35 validation procedures and 30 forms that can be used to establish a validation documentation system and provides protocol templates readers can use as their own. Numerous diagrams and graphics are used to illustrate key points.
Vendeur : HPB-Red, Dallas, TX, Etats-Unis
EUR 182,06
Quantité disponible : 1 disponible(s)
Ajouter au panierHardcover. Etat : Good. Connecting readers with great books since 1972! Used textbooks may not include companion materials such as access codes, etc. May have some wear or writing/highlighting. We ship orders daily and Customer Service is our top priority!
Vendeur : Basi6 International, Irving, TX, Etats-Unis
EUR 201,49
Quantité disponible : 8 disponible(s)
Ajouter au panierEtat : Brand New. New. US edition. Expediting shipping for all USA and Europe orders excluding PO Box. Excellent Customer Service.
Vendeur : Romtrade Corp., STERLING HEIGHTS, MI, Etats-Unis
EUR 202,03
Quantité disponible : 2 disponible(s)
Ajouter au panierEtat : New. This is a Brand-new US Edition. This Item may be shipped from US or any other country as we have multiple locations worldwide.
Vendeur : SMASS Sellers, IRVING, TX, Etats-Unis
EUR 210,82
Quantité disponible : 2 disponible(s)
Ajouter au panierEtat : New. Brand New Original US Edition. Customer service! Satisfaction Guaranteed.
Vendeur : SMASS Sellers, IRVING, TX, Etats-Unis
EUR 213,06
Quantité disponible : 2 disponible(s)
Ajouter au panierEtat : New. Brand New Original US Edition. Customer service! Satisfaction Guaranteed.
EUR 248,08
Quantité disponible : 1 disponible(s)
Ajouter au panierEtat : New. pp. 456 1st Edition.
EUR 272,96
Quantité disponible : Plus de 20 disponibles
Ajouter au panierEtat : New. Phil CloudWhile FDA regulations, cGMP, GLP, GCP, and the industry standard ISO 9000 require that documentation be established and followed, they do not provide guidelines on how to produce that documentation. Pharmaceutical Equipment Validation gives de.
EUR 349,38
Quantité disponible : 3 disponible(s)
Ajouter au panierEtat : New. pp. 456.
Langue: anglais
Edité par Taylor & Francis Inc Aug 1998, 1998
ISBN 10 : 1574910795 ISBN 13 : 9781574910797
Vendeur : AHA-BUCH GmbH, Einbeck, Allemagne
EUR 338,50
Quantité disponible : 2 disponible(s)
Ajouter au panierBuch. Etat : Neu. Neuware - Comprehensively covering equipment qualification and process validation for pharmaceutical process equipment, this text shows readers how to demonstrate compliance, what data to use, and how to produce the appropriate documentation. The author delineates how to prepare, test, and complete equipment qualification protocols. He also explains how to perform qualification testing and whether to test the equipment for a worst-case scenario. The thirty-eight completed protocol templates cover specific equipment types, provide instant answers to most protocol writing and testing questions, show how to qualify each piece of equipment, and provide a check for readers' own protocols.
Vendeur : Majestic Books, Hounslow, Royaume-Uni
EUR 72,90
Quantité disponible : 3 disponible(s)
Ajouter au panierEtat : New. pp. 375 This item is printed on demand.
Vendeur : Biblios, Frankfurt am main, HESSE, Allemagne
EUR 78,69
Quantité disponible : 4 disponible(s)
Ajouter au panierEtat : New. PRINT ON DEMAND pp. 375.
Vendeur : Majestic Books, Hounslow, Royaume-Uni
EUR 253,65
Quantité disponible : 1 disponible(s)
Ajouter au panierEtat : New. pp. 456 This item is printed on demand.