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Does a manufacturer have a duty to warn potential users of a potentially harmful product? If so, where does the duty to warn arise and to what standard will a manufacturer be held liable?
Does the Business Practices and Consumer Protection Act apply to a hospital in British Columbia, which implanted a pacemaker into a patient? How would the patient's consent be treated in such case?
Is there a cause of action whereby XXX can sue YYY for the unauthorized use of party A's barcode on product's packaging?
What do retailers need to know about the Canada Consumer Product Safety Act?
What is the Competition Bureau's approach to assessing “Made in Canada” and “Product of Canada” claims?
What is the Government of Canada's approach to regulating payment card network operators and their participants?
What is the purpose, content of, and the laws and legal issues that the Environmental Claims: A Guide for Industry and Advertisers is meant to address?
What legal issues and laws were raised by the motion to authorize a national class action instituted in the Province of Quebec against Gaiam Inc. for false and misleading advertising related to its claim that its reusable aluminum water bottle was Bisphenol A(BPA) free?
When do regulations extending the Good Manufacturing Practices (“GMP”) to Active Pharmaceutical Ingredients (“APIs”) come into force? What are the requirements under the GMP for APIs in the new regulations? What is a Quality Assurance Agreement?
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