Method Validation in Pharmaceutical Analysis: A Guide to Best Practice

This second edition of a global best–seller has been completely redesigned and extensively rewritten to take into account the new Quality by Design (QbD) concept in pharmaceutical manufacturing. As in the first edition, the analytical requirements during the entire product lifecycle are covered, but now a new section is included on continued performance monitoring and the transfer of analytical procedures. Two case studies from the pharmaceutical industry illustrate the concepts and guidelines presented, and the standards and regulations from the US (FDA), European (EMA) and global (ICH) regulatory authorities are considered throughout. The undisputed gold standard in the field. INDICE: INTRODUCTION Analytical Validation within the Pharmaceutical Lifecycle ANALYTICAL EQUIPMENT QUALIFICATION Analytical Instrument and System Qualification Efficient and economic HPLC Performance Qualification ESTABLISHMENT OF MEASUREMENT REQUIREMENTS Analytical Target Profile and Decision Rules Performance Based Specifications METHOD PERFORMANCE CHARACTERISTICS Precision Accuracy and Range Specificity Linearity Detection and Quantitation Limit Glossary METHOD DESIGN AND UNDERSTANDING Method Selection, Development and Optimisation Analytical Quality by Design and Robustness Investigations Case Study Robustness Investigations System Suitability Tests METHOD PERFORMANCE QUALIFICATION Case Study: Qualification of an HPLC Method for Identity, Assay, and Degradation Products Design and Qualification of a Delivered Dose Uniformity Procedure for a Pressurised Metered Dose Inhaler Implementation of Compendial/Pharmacopeia Test Procedures Transfer of Analytical Procedures CONTINUED METHOD PERFORMANCE VERIFICATION Routine Monitoring Investigating and Addressing Aberrant Data Continual Improvement

• ISBN: 978-3-527-33563-3
• Editorial: Wiley VCH
• Encuadernacion: Rústica
• Páginas: 480
• Fecha Publicación: 25/09/2014
• Nº Volúmenes: 1
• Idioma: Inglés