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Step-by-Step Analytical Methods Validation and Protocol in ...
Step-by-Step Analytical Methods Validation and Protocol in the Quality System Compliance Industry BY GHULAM A. SHABIR.. Introduction peatability and intermediate precision), specificity, detec- Methods Validation : Establishing documented evidence tion limit, quantitation limit, linearity, range, and robustness that provides a high degree of assurance that a specific (Figure 1). In addition, Methods Validation information method, and the ancillary instruments included in the should also include stability of Analytical solutions and sys- 7. method, will consistently yield results that accurately reflect tem suitability. the quality characteristics of the product tested. Health Canada (HC) has also issued guidance on meth- 8. Method Validation is an important requirement for any ods Validation entitled Acceptable Methods Guidance. HC. package of information submitted to international regula- has been an observer of ICH, and has adopted ICH guide- tory agencies in support of new product marketing or clini- lines subsequent to its reaching Step Four of the ICH.
dissolution, biological methods), and provides acceptance criteria for validation parameters and system suitability tests for all methods. HC has also issued templates recommended as an ap-proach for summarizing analytical methods and validation data ICH terminology was used when developing these tem-plates.
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