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