This seminar will give an overview on ICH Q3D and USP approaches to specify and control elemental impurities to below toxic limits in drug products and ingredients. The seminar will discuss in detail selected elements, limits and analytical procedures.
Elemental Impurities According to the new ICH Q3D and USP 232/233 Guidelines
17 October 2013, United States
Introduction
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Online
Online, United States
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Labcompliance
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