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Toxicology GLP Monitoring

Our GLP-trained staff can assist biotechnology, pharmaceutical, and medical device companies meet GLP expectations, including U.S. 21 CFR 58, Canadian, ICH, and OECD requirements. Intertek Cantox strategic auditing and scientific monitoring can help companies avoid repetition of studies, clinical holds, and additional costs:

  • Pre-placement audits of contract research facilities;
  • Monitor nonclinical study initiation and progress;
  • Assistance to sponsors in preparations for inspections and due diligence activities.
 

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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Accessibility for Ontarians with Disabilities (AODA)

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