Canadian Institutes of Health Research
570,556 snapshots · latest May 3, 2026
Homepage:https://cihr-irsc.gc.ca/
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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 This is an archive — not current guidance or medical advice. Archived content may be incomplete, outdated, or superseded.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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Health Canada
386,223 snapshots · latest Apr 14, 2026
Public Health Agency of Canada
243,880 snapshots · latest Apr 28, 2026
Toronto 2015 Pan American and Parapan American Games - Importing and Exporting Controlled Substances, Precursor Chemicals and Therapeutic Products The Government of Canada regulates the importation and exportation of controlled substances, precursor chemicals and therapeutic…
Guidance on medical device compliance and enforcement (GUI-0073): Overview Overview Compliance and enforcement Response to non-compliance Glossary References Relevant regulations Effective date : December 14, 2024 Replaces: Guidance on Medical Device Compliance and Enforcement…
Notice to Stakeholders - Updates to drug establishment licence applications and good manufacturing practice evidence requirements for active pharmaceutical ingredients Canada's Food and Drug Regulations (Regulations) were amended to extend the requirements of Division 1A -…
Good manufacturing practices for medical gases (GUI-0031) - Summary Good manufacturing practices (GMP) guidelines for drug products (GUI-0001) Guidance on Drug Establishment Licences and Drug Establishment Licensing Fees (GUI-0002) Risk classification guide for drug good…
Consultation on the Revised Inspection Strategy for Licensed Blood Establishments Current status: CLOSED Health Canada conducts inspections of establishments that process blood for transfusion and for manufacture into a drug for human use. Health Canada will be engaging with…
Guidelines for environmental control of drugs during storage and transportation (GUI-0069) PDF format (PDF format, 1085 KB, 23 pages) Organisation : Health Canada Date issued: August 2020 Disclaimer This document does not constitute part of the Food and Drugs Act (the Act) or its…
Risk classification guide for drug good manufacturing practices observations (GUI-0023) - Summary Overview These guidelines establish the approach applied for both the attribution of risk ratings to observations noted during drug establishment inspections, and the overall rating…
Regulatory requirements for importing medical devices On this page What is commercial importation Who can import Unlicensed and counterfeit medical devices Compliance and enforcement actions Contact us Medical devices are products used to treat, mitigate, diagnose or prevent a…
New one-stop web page for the medical device industry MDCP Bulletin February 8, 2022, from the Medical Devices Compliance Program On this page About the new landing page What you'll find Benefits to you About the new landing page Manufacturers, importers and distributors must…
Health Canada will continue to issue electronic manufacturer’s certificate to export MDEL Bulletin, August 23, 2022, from the Medical Devices Compliance Program On this page Background Why we're continuing to issue electronic certificates What to expect Authentication and…
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