Method Development and Validation Services

Validation of an analytical procedure is an essential process in the GMP analysis of a pharmaceutical product.  This can include Limit tests for the control of impurities and  quantitative tests of the active in drug products.  Validation parameters as set out by the International Committee on Harmonisation (ICH) are followed.Assay, Impurity and Stability Indicating methods utilizing techniques such as  HPLC, LC/MS, GC, GC/MS, ICP/OES, ICP/MS and Ion Chromatography are available.