Moredun offers comprehensive assistance with the design of pharmacokinetic/pharmacodynamic, bioequivalence and marker residue studies to investigate the ADME (Administration/Distribution/ Metabolism/Excretion) profile of veterinary pharmaceuticals in biological systems.
Analytical method development and validation can also be undertaken through experienced commercial partners, in accordance with relevant legislation and guidelines. In this way we are able to offer the complete regulatory study package for PK and disease model studies from the initial planning of the study through the animal phase and then to the analysis of the resulting samples.
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