Data from all assay platforms fulfilled certain requirements for immunogenicity evaluation collection from the EMA and FDA 2, 3. The LoQ (0008?g/ml) for UST quantification dependant on the empirical strategy seems to contradict the LoD (025?g/ml) (Desk ?(Desk1).1). and quantitation limitations, linearity, range, accuracy, selectivity and accuracy. Quantitation of UST and ADA was feasible at […]