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Browse and search historical snapshots. This is an archive — not current guidance or medical advice. Archived content may be incomplete, outdated, or superseded. For up-to-date recommendations, always consult the official source website.
For background on coverage and capture methods, see Methods & coverage.
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Exceptional importation and sale of biocides in relation to COVID-19: For industry List of designated biocides For industry On this page About the new regulations and exceptional importation How to import and sell designated biocides Regulatory requirements for selling designated…
Exceptional importation and sale of drugs in relation to COVID-19: For industry Overview Tier 3 drug shortages List of designated drugs For industry On this page How to propose an addition to the list of designated drugs How to import and sell designated drugs Regulatory…
Explanatory note: Interim order No. 2 extends measures for drugs, medical devices and foods for a special dietary purpose Alert for Explanatory note: Interim order No. 2 extends measures for drugs, medical devices and foods for a special dietary purpose Health Canada published…
Health Canada Decision-Making Framework for Identifying, Assessing, and Managing Health Risks - August 1, 2000 (PDF Version - 328 K) Table of Contents Preface Background Project Overview Contributors Purpose of the Framework and Guidance Documents Intended Audience Intended…
Politique de conformité et d’application de la loi pour la Loi sur la procréation assistée (POL-0100) Avis de non responsabilité Le présent document ne fait pas partie de la Loi sur la procréation assistée (la Loi) ou de ses règlements. En cas de contradiction ou…
A guide to Health Canada inspections On this page Health Canada's mandate and authorities Regulated parties are subject to inspections What to expect from a Health Canada inspection Inspections and the rights and responsibilities of a regulated party Zero tolerance for harassment…
New e-learning course on understanding how medical devices are regulated in Canada MDCP Bulletin, October 28, 2022, from the Medical Devices Compliance Program On this page Background About the course Target audience How to access the course Contact us Background The Medical…
Contact the Medical Devices Compliance Program You can contact the Medical Devices Compliance Program by choosing from the list of topics below: Expand all Hide all For fee related questions Email: criu-ufrc@hc-sc.gc.ca For inquiries about Medical Device Shortages Email:…
Completed drug and health product compliance monitoring projects Once we complete a project, we make the results available to the public. Learn more about the compliance monitoring projects we have conducted to date. Drugs 2022: Canadian Specific Opioid targeted Risk Management…
Foreign risk notification for medical devices guidance document: What, when and how to submit Background Definitions Responsibilities and notifiable actions What, when and how to submit Monitoring, compliance and enforcement On this page Information to submit Timelines How to…
Early release: coverage is bounded to the current corpus, and features may change.
