| Select | Title | Policy Type | Year |
|---|---|---|---|
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Regulatory framework for the mandatory reporting of adverse drug reactions and medical device incidents by provincial and territorial healthcare institutions. | Response to consultation | 2016 |
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Front-of-package labelling consultation | Response to consultation | 2016 |
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Regulation of Self-Care Products in Canada | Response to consultation | 2016 |
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Health Canada’s Consultation on “Plain and Standardized Packaging” | Response to consultation | 2016 |