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B01=Joachim Ermer
B01=Phil W. Nethercote
Category1=Non-Fiction
Category=PN
COP=Germany
Delivery_Pre-order
Language_English
PA=Not yet available
Price_€100 and above
PS=Forthcoming
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Method Validation in Pharmaceutical Analysis: A Guide to Best Practice

English

New edition of the gold standard in the field of pharmaceutical analysis, extensively updated to include the new ICH Guidelines Q2 and Q14

Following an all-encompassing lifecycle approach to analytical procedures in pharmaceutical analysis, Method Validation in Pharmaceutical Analysis provides hands-on information for readers involved in development, validation, and continued maintenance and evaluation of analytical procedures in pharmaceutical analysis.

This newly revised and updated Third Edition includes much-needed interpretation of the most recent ICH guidelines for validation and method development, as well as recent publications of the USP Validation & Verification Expert Panel on Analytical Procedure Lifecycle Management and the activities of the British Pharmacopeia AQbD Working Party. It also addresses trending topics in the field such as data integrity and continuous monitoring of analytical performance.

Written by a team of highly qualified pharmaceutical professionals, Method Validation in Pharmaceutical Analysis includes information on sample topics such as:

  • Data governance, data integrity, and data quality, as well as analytical instrument qualification and system validation lifecycle
  • Continued HPLC performance qualification, analytical target profile, decision rules and fitness for intended use, and performance characteristics of analytical procedures
  • Method selection, development, and optimization, multivariate analytical procedures, and risk assessment and analytical control strategy
  • Implementation of compendial/pharmacopeia test procedures, transfer of analytical procedures, and the lifecycle approach to transfer of analytical procedures

Completely comprehensive in coverage, Method Validation in Pharmaceutical Analysis is an essential reference for scientists, researchers, and professionals in the pharmaceutical industry, analytical chemists, QA officers, and public authorities tasked with relevant regulatory responsibilities.

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Current price €155.79
Original price €163.99
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Age Group_Uncategorizedautomatic-updateB01=Joachim ErmerB01=Phil W. NethercoteCategory1=Non-FictionCategory=PNCOP=GermanyDelivery_Pre-orderLanguage_EnglishPA=Not yet availablePrice_€100 and abovePS=Forthcomingsoftlaunch

Will deliver when available. Publication date 05 Feb 2025

Product Details
  • Dimensions: 170 x 244mm
  • Publication Date: 22 Jan 2025
  • Publisher: Wiley-VCH Verlag GmbH
  • Publication City/Country: Germany
  • Language: English
  • ISBN13: 9783527348909

About

Joachim Ermer is Head of QC Lifecycle Management Chemistry at Sanofi in Frankfurt Germany. He is also Global Reference Standards Coordinator and responsible for the Reference Standards Logistic group in Frankfurt. Phil W. Nethercote was the analytical leader for the Global Manufacturing and Supply Division of GSK until he retired in 2016. He has over 30 years of experience in the pharmaceutical industry the majority of which has been with Glaxo Glaxo Wellcome and GSK.

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