Pre-clinical Toxicology

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
Tel. +33 (0) 557 77 56 10
Fax. +33 (0) 557 77 56 20
CEHTRA France SAS
43-45 rue Laroque
33560 Sainte Eulalie, France
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