For regulatory toxicology studies it is required to analyse the dose formulations given to the animals for test item concentration and homogeneity. Usually, the analysis will be performed using UV-HPLC, but other techniques might also be relevant. If the client do not have the capabilities or resources to do this, Scantox offers to perform the analysis of dose formulations including validation of the method.

Non-clinical Dose Formulation Analysis

The analyses and validation will be performed as described in the white paper on non-clinical dose formulation analysis (see Whitmire et al, 2010, link til pubmed?). The validation can include the following parameters: specificity, sensitivity, linearity, range, precision, accuracy, homogeneity and stability.

Scantox Dose formulation analysis