Registering a Hand Sanitizer in Canada
By: Sarah Calder, Regulatory Affairs Specialist, email Does a hand sanitizer require pre-approval in Canada before going to market? Hand sanitizers, hand sanitizing wipes, and antibacterial hand [...]
Chemical Regulatory Compliance Training
By: Kirsten Alcock, Manager of Product Safety, email Training. Where do you obtain it? What if you have something so specific that training is simply not available? There are plenty of free [...]
Health Products Compliance Monitoring
By: Sarah Calder, Regulatory Affairs Specialist, email Importers, manufacturers, and distributors of health products regulated under the Food and Drugs Act who advertise in Canada must ensure [...]
Amendments to the Fertilizers Regulations (Fertilizer Modernization)
By: Teri Dickinson, Regulatory Affairs Group Manager, email The Canadian Food Inspection Agency’s (CFIA) modernization of the Fertilizers Regulations is part of a multi-year initiative to [...]
Medical Device Establishment Licensing (MDEL) Post Market Cost Recovery
By: Teri Dickinson, Regulatory Affairs Group Manager, email Starting April 1, 2020, new medical device Establishment Licensing (MDEL) fees will come into effect. What can you expect to pay? Not [...]
Medical Devices: Evaluation and Right to Sell Fees
By: Teri Dickinson, Regulatory Affairs Group Manager, email Are you ready for Cost Recovery implementation coming into force on April 1, 2020? Starting April 1, 2020, new medical device [...]
Veterinary Health Products (VHPs) Cost Recovery
By: Teri Dickinson, Regulatory Affairs Group Manager, email All companies are required to notify Health Canada about their Veterinary Health Products (VHPs). This must be done: At least 30 days [...]
Veterinary Drugs (Evaluation and Right to Sell Fees)
By: Teri Dickinson, Regulatory Affairs Group Manager, email Are you ready for Cost Recovery implementation coming into force on April 1, 2020? You may want to get your submissions in now. Other [...]
