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Final fill for mAbs Progressing from the drug substance to the final injectable drug product requires final packaging vials and stoppers that meet a number of quality requirements. To meet these requirements products must be prepared in an ISO Cla...

Nucleic Acid decontamination with DNA Exitus Plus Technology DNA-Exitus Plus™ is a novel patented reagent for the removal of nucleic acid contamination from laboratory surfaces and equipment. Instructions for use: The optimal incubation time for s...

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Gehaltsbestimmung von Ca und Mg in Mineralwässern Application date: 20.06.2013 page 1 from 10 Determination of isocyanate (NCO-) content Application date: 20.06.2013 page 2 from 10 Use This method is applicable for material containing reactive iso...

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Upstream processing for cell therapy Compared to production volumes associated with other biologics (e.g. mAbs: 2000L to 10000L) cell therapy production volumes are more commonly between 1L to 10L. Even the quality parameters are different. Instea...

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Upstream processing for mAbs Developing and manufacturing mAbs has moved away from a dependency on raw materials of animal origin. Our biochemical components and supplements are animal component-free to meet the needs of these applications. Produc...

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