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Toxicology Consulting

Intertek Cantox specializes in providing expert toxicological and regulatory strategies for pharmaceutical and emerging biopharmaceutical companies. Our strength lies in providing solutions to complex development, toxicological, and regulatory issues, through the combined expertise of both our scientific and regulatory staff. Our industry-leading toxicology consulting services include:

  • Design, implementation, and management of nonclinical testing programs with a focus on company goals (e.g., First-in-Human trials and achieving Proof of Concept);
  • Review, interpretation, and positioning of data (toxicology study reports, literature, safety data);
  • Toxicology issues resolution, including interactions with regulatory authorities and the preparation of “white papers”;
  • Gap analysis and independent data reviews;
  • Impurities and excipients assessments, risk/safety assessments, and hazard identification;
  • Pre/Post-marketing toxicology consulting.
 

Are you in compliance with the regulations affecting cosmetic products?
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What’s New

Intertek Cantox Opens an Office in Beijing, China.
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Don't Miss our Workshop on the Regulation of Animal Feed Ingredients in the United States.
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Learn more about the Environmental Assessment Regulations and the In-Commerce List for Food & Drug Act Substances and how our services can help support your company’s business interests.
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If your company has been notified of a violation of the California Prop 65 law for your products, we offer a variety of services that may helpful in responding to this notice.
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Cantox is pleased to offer expertise in Nanotechnology and Veterinary Nutraceuticals.

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Canada

Mississauga, ON
905-542-2900
United States

Bridgewater, NJ
(908) 429-9202
Europe

Fleet, Hampshire, UK
+44 (0) 1252 400 505
Asia

Tokyo, Japan
+81-3-5639-9158
 
info@cantox.com