Enabling you to identify and mitigate the intrinsic risk in your operations, supply chains and business processes.
Evaluating how your products and services meet and exceed quality, safety, sustainability and performance standards.
Validating the specifications, value and safety of your raw materials, products and assets.
Joanne Wan, Ph.D., DABT Senior Program Manager, Toxicology
Since joining Intertek Scientific & Regulatory Consultancy (formerly Cantox) in 2007, Dr. Wan has helped our clients address specific reproductive and developmental toxicology issues. She assists clients with the design and implementation of nonclinical toxicology programs in areas such as oncology drugs, antiinfectives, and dermal products. Dr. Wan also conducts critical reviews of data and reports with a view towards submission writing, including Investigator’s Brochures and Nonclinical Summaries. Her involvement with nonclinical development programs also includes nonclinical Contract Research Organization (CRO) site selection visits, and on-site monitoring of nonclinical studies for scientific integrity and adherence to the principles of Good Laboratory Practice (GLP).
In addition to these activities, Dr. Wan also conducts toxicology safety and risk assessments for product impurities, excipients, extractables and leachables and assists clients with efficacy claims for cosmetic, natural health products, and dietary supplements.
Her research has been recognized in the form of scholarship awards from the Canadian Institutes of Health Research and the Canadian Cancer Society Research Institutes’ Programme of Research in Environmental Etiology of Cancer. She is a member of the Society of Toxicology (SOT).
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