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Compliance

As millions of dollars are invested in the research and development of new drug products, the integrity of work must be maintained so as not to face costly and unnecessary delays. Both GLP and GMP compliance are supported by these activities:

  • Review of nonclinical study reports and protocols to ensure GLP compliance;
  • GMP audits for clinical trial materials (API and fill/finish facilities);
  • Assistance in the development of a compliance program; 
  • Ad hoc consultations regarding compliance;
  • GLP monitoring of nonclinical studies and facilities.
 

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