CEHTRA toxicologists have a vast experience of writing and reviewing regulatory submissions (including IND, NDA and CTX submissions, and pharmaco-toxicological expert reports). Under such a programme we can help you with any or all of the following:
Provision of scientific input into compound development programmes and strategies
Supervision of contract toxicology development programmes
Evaluation and/or audit of contract laboratories and monitoring of individual contract toxicology studies
Interaction with regulatory agencies regarding preclinical toxicology and pathology issues
