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USP <232>/<233> and ICH Q3D Elemental Impurities Analysis: The Agilent ICP-OES Solution

Technické články | 2021 | Agilent TechnologiesInstrumentace
Software, ICP/OES
Zaměření
Farmaceutická analýza
Výrobce
Agilent Technologies
Klíčová slova
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White Paper USP <232>/<233> and ICH Q3D Elemental Impurities Analysis: The Agilent ICP-MS Solution Elemental Impurity Analysis Requirements Worldwide, regulatory authorities are responsible for ensuring that pharmaceutical products are both effective and safe. Potentially toxic and harmful contaminants—including elemental impurities—must…
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Proposed new ICH and USP methods for elemental impurities: The application of ICP-MS and ICP-OES for pharmaceutical analysis White paper Authors Amir Liba, Ed McCurdy and Ross Ashdown Agilent Technologies Abstract The United States Pharmacopeial Convention (USP), in parallel with…
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Application Note Pharmaceuticals Validating performance of an Agilent ICP‑MS for USP <232>/<233> & ICH Q3D(R2)/Q2(R1) Reducing the time and expense of ICP-MS method development and system validation for measuring elemental impurities in pharmaceuticals Authors Lindsey Whitecotton, Ed McCurdy, Craig Jones…
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Measuring Elemental Impurities in Pharmaceutical Materials
2022|Agilent Technologies|Brožury a specifikace
Measuring Elemental Impurities in Pharmaceutical Materials Agilent Atomic Spectroscopy Solutions USP <232>/<233> & ICH Q3D(R2)/Q2(R1) Implementing Elemental Impurities Tests in the Pharmaceutical Industry Worldwide regulations for pharmaceutical materials Worldwide pharmacopeias have introduced revised standards for controlling elemental impurities in drug…
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