Transcription of PHARMACEUTICAL MANUFACTURING HANDBOOK
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PHARMACEUTICAL MANUFACTURING HANDBOOKR egulations and QualitySHAYNE COX GAD, , Consulting ServicesCary, North CarolinaA JOHN WILEY & SONS, INC., PUBLICATIONPHARMACEUTICAL MANUFACTURING HANDBOOKR egulations and QualityPHARMACEUTICAL MANUFACTURING HANDBOOKR egulations and QualitySHAYNE COX GAD, , Consulting ServicesCary, North CarolinaA JOHN WILEY & SONS, INC., PUBLICATIONC opyright 2008 by John Wiley & Sons, Inc. All rights reservedPublished by John Wiley & Sons, Inc., Hoboken, New JerseyPublished simultaneously in CanadaNo 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, scanning, or otherwise, except as permitted under Section 107 or 108 of the 1976 Unit
Analytical Method Validation and Quality Assurance. Erik Van Bockstaele, Institute for Agricultural and Fisheries Research (ILVO), Scientifi c Institute for the Flemish Community, Merelbeke, Belgium, Analytical Method Validation and Quality Assurance. T. Vasconcelos, Laboratory of Pharmaceutical Development, BIAL, Mamede do
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