We provide an extensive analytical service to ensure accurate formulation and dosing concentrations for successful toxicology studies. Formulation analysis is an essential support service for GLP toxicology studies and is often advisable on non-GLP studies when accuracy of dosing concentration is critical. We offer a comprehensive formulation analysis service by our specialist team. Alderley Analytical has considerable experience in analytical method development and validation, as well as the subsequent analysis of dose formulation samples.
Achieved concentrations of dose formulations is a regulatory requirement for GLP toxicology studies. Analysis of dose formulations, whether solutions or suspensions is required to verify the concentration accuracy and homogeneity of the formulation used for in-vivo dosing (or in vitro testing) during pre-clinical programs. Stability of the dose formulations under the conditions of the study is also verified.
Analyses are performed by highly trained personnel who have a wide range of scientific skills and many years of experience. Method development is conducted by experienced staff who are responsible for the efficient transfer of clients’ methods, the development of assays from first principles, or the modification of existing methods as necessary.