This toolkit highlights the most comprehensive information on analytical method validation and method development. With over 150 pages from the Journal of Validation Technology and the Journal of GXP Compliance, two hours of pre-recorded webinars, and thousands of slides from IVT's annual method validation conference, these products will ensure you keep abreast of ongoing method strategies and global regulatory trends.
Products in this Toolkit
Validating Immunoassays Using the Fluorescence Polarization Assay for the Diagnosis of Brucellosis David Gall and Klaus NielsenStep-by-Step Analytical Methods Validation and Protocol in the Quality System Compliance Industry Ghulam A. ShabirGood Analytical Method Validation Practice: Setting Up for Compliance and Efficiency: Part I Stephan O. Krause, Ph.D.Good Analytical Method Validation Practice: Deriving Acceptance Criteria for the AMV Protocol: Part II Stephan O. Krause, Ph.D.Download the entire
Biological Method Validation A Practical Approach Cindy GreenDefining a Master Plan for the Validation of Analytical Methods Paul A. Winslow, Ph.D. and Richard F. Meyer, Ph.D.FDA and Industry Address Analytical Validation Issues for the Pharmaceutical Industry Jerry Lanese, Ph.D.Guidance for Industry Bioanalytical Methods Validation for Human Studies US Food and Drug Adminstration
FDA’s New Process Validation Guidance: How Can It Impact Test Method Validation? Jerry Lanese, Ph.D., President, The Lanese Group LLCEnsure Method Validation Compliance through Review of FDA Warning Letters David T. Lin, Ph.D., Senior Consultant, Biologics Consulting Group, Inc. Enhancing Analytical Quality Through the Use of UPLC: One Method in Place of Two Corinne Mounier-Lee, Ph.D, Principal Scientist, Catalent Pharma SolutionsApplying QbD Based on Risk Assessment to Achieve a Fundamental & Practical Understanding of Method Validation Sue Mecham, Ph.D., Director of Laboratory...
In this 2009 webinar, Sam Venugopal discusses the results of CRADA's FDA-sponsored study on identifying the bottlenecks for implementation of quality by design (Qbd) in manufacturing facilities and opportunities for improvement. Download "Understanding the Challenges Behind QbD – A Review of Leading Practices"
Establish good documentation practices and acceptance criteriafor method validationOptimize methods and effectively communicate experimental resultsHandle deviations and variations during method validationDevelop change control processes during method validationReport your validation results—Streamline the processDevelop and validate of NIR/supervised principal component analysis methodsDiscover a new experimental approach for robustness experimentsDevelop and validate of chromatographic methodsValidate and verifiy of compendial methodsDownload the 8th Annual Method Validation AgendaDownload...
Hear directly from FDA and USP to Stay Abreast of Evolving Guidelines and RegulationsApply a QbD and Risk Management Approach to Method ValidationsLearn What is Needed to Update Your Methods to Today’s StandardExamine Different High Throughput Method Development StrategiesQualify Analytical InstrumentsDownload the 9th Annual Method Validation and Development AgendaDownload the 9th Annual Method Validation and Development Compendium
Method Validation Studies: How GLP Interacts with Guidance Documents Steven S. Kuwahara, Ph.D.Reduction of Analytical Method Variability in an R&D Laboratory: A Case Study Briank K. Nunnally, Andre Johnson, and Raymond KaiseMethod Validation (for Medical Devices) Laure LarkinUse of Monte Carlo Simulation to Address CMC Issues Harry Yang, Ph.D.Validation of Dissolution Methods Gregory P. Martin and Vivian GrayUSP <1010> Analytical Data-Interpretaion and Treatment Appendix E: Comparison of Methods Lynn TorbeckAddressing Compliance Concerns During Dissolution Method Development, Validation,...
Understand the regulators' expectations for QbDMake the business case for a QbD programUnderstand what new / additional expertise will be needed to:Establish a design spaceDescribe a design space in the submission.