Practical HPLC and LC-MS Method Development and Validation : Guidelines for Pharmaceutical Scientists / Ghulam A. Shabir

Public ISBD Titre : Practical HPLC and LC-MS Method Development and Validation : Guidelines for Pharmaceutical Scientists Type de document : texte imprimé Auteurs : Ghulam A. Shabir, Auteur Editeur : LAP Lambert Academic Publishing Année de publication : 2012 ISBN/ISSN/EAN : 978-3-659-12352-8 Langues : Français (fre) Catégories : Biochimie Résumé : The coherent body of research described in this book is concerned with new HPLC method development and validation using novel systematic approaches for pharmaceutical and diagnostic compounds. The first stage of the research was to study how analytical method development and validation are typically carried out at present and to formulate this into a simple step-by-step approach. Such a template and protocol was not only used as the foundation of this research programme but could also serve as a simple systematic guide for other practitioners and those new to the field. Furthermore, it was recognised that this protocol should satisfy the requirements of the most strategically important regulatory agencies. The second stage of this research involved evaluation and application of the above validation approach to new methods that were developed for a diverse range of analytes using HPLC and LC-MS. In essence, the critical review of the requirements for method validation for various agencies and the subsequent preparation of guidelines on how to go about method validation have had a significant impact on analytical practitioners worldwide. Practical HPLC and LC-MS Method Development and Validation : Guidelines for Pharmaceutical Scientists [texte imprimé] / Ghulam A. Shabir, Auteur . - [S.l.] : LAP Lambert Academic Publishing, 2012. ISBN : 978-3-659-12352-8 Langues : Français (fre) Catégories : Biochimie Résumé : The coherent body of research described in this book is concerned with new HPLC method development and validation using novel systematic approaches for pharmaceutical and diagnostic compounds. The first stage of the research was to study how analytical method development and validation are typically carried out at present and to formulate this into a simple step-by-step approach. Such a template and protocol was not only used as the foundation of this research programme but could also serve as a simple systematic guide for other practitioners and those new to the field. Furthermore, it was recognised that this protocol should satisfy the requirements of the most strategically important regulatory agencies. The second stage of this research involved evaluation and application of the above validation approach to new methods that were developed for a diverse range of analytes using HPLC and LC-MS. In essence, the critical review of the requirements for method validation for various agencies and the subsequent preparation of guidelines on how to go about method validation have had a significant impact on analytical practitioners worldwide.

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Code-barres	Cote	Support	Localisation	Section	Disponibilité
6364	Bioch 52	Livre	Bibliothèque	Biochimie	Exclu du prêt

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