With 37 years of experience in toxicology in the areas of preclinical pharmaceutical development, medical devices and related subjects, Andrew has a significant understanding of the scientific and regulatory requirements in these fields.

Working in Contract Research, first in the UK, and subsequently in Denmark, he has gained a very broad understanding of the needs of customers from a wide variety of different companies and approaches, from small (virtual) companies all the way up to Big Pharma.  His work involves all aspects of the process from identifying the needs of the customer through to execution of projects and interpretation of study results.

As a result of working in multi-national organisations, the varied needs of a global customer base are of great importance to him, and the customer is always the focus.