Monique Wells, VMD, MS, DACVP, DECVP, DABT, Eurotox-registered toxicologist

[Dr. Wells has worked for the chemical (Chevron), pharmaceutical (Rhône-Poulenc Rorer; currently Sanofi-Aventis) and cosmetics (L’Oréal) industries in the U.S. and in France prior to entering consulting in 2002. She has extensive experience in preparing expert reports and regulatory documentation for companies in North America, Europe and Asia. Her most recent first-author journal publications feature the investigation of vascular lesions of the skin in subcutaneous toxicity studies performed in rats. Dr. Wells is the author of the chapter, ”Data Analysis, Report Writing and Regulatory Documentation” in Pharmaceutical Toxicology in Practice: A Guide for Non-Clinical Development (John Wiley & Sons, Inc, 2011).

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