DDS offer targeted, bespoke screening and quantitative analysis of elemental impurities in final products, excipients, APIs, raw materials, and packaging materials from DDS's state-of-the-art cGMP facility in Cambridge (Fordham), UK. DDS's reliable and accurate analysis is in accordance with ICH Q3D and USP guidelines, using a combination of ICP-MS and ICP-OES as appropriate. This combination enables us to measure down to the low ppb or ppt levels required for impurity quantification in high dose materials up to ppm or wt% levels where an assay is required.
DDS also offers speciation analysis for As, Hg, and other elements to ensure compliance and to help investigate process chemistries and reaction studies.
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Manufacturer Resolian | Available Worldwide
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