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. https://pharmaceutical.report/Resources/Whitepapers/79bc0970-609b-481f-ac5f-248f6317a481__en_assets_EDXRF-white%20paper_tcm50-45607.pdf
whitepaper
SHARESHARESHARE
THE USE OF EDXRF FOR PHARMACEUTICAL MATERIAL ELEMENTAL ANALYSIS
The recent changes to the United States Pharmacopeia (USP) regarding requirements for elemental impurity testing has peaked interest into new ways to perform this testing. Combining these new requirements with the introduction of USP chapter <735> X-ray fluorescence spectrometry1 permits a new alternate method for quantifying elemental impurities in pharmaceutical materials. DOWNLOAD