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List of Drugs for an Urgent Public Health Need The List of Drugs for an Urgent Public Health Need (the List) contains the following drug-related details: the brand name, the medicinal ingredient(s), the route of administration, the strength, the dosage form and the identifying…

Improving the regulatory review of drugs and devices – stakeholder meetings and engagement activities In keeping with our commitment to openness and transparency, a notice was posted to inform stakeholders on how Health Canada will handle meeting and correspondence information…

Information and privacy notice for specific Health Products and Food Branch initiatives On this page No Confidentiality Privacy Notice The following notice explains how Health Canada will handle information from meetings and correspondence with stakeholders related to the…

How Health Canada engages and informs Canadians Part of Health Canada’s work as a regulator is to engage and inform Canadians on issues about their health. Learn how we use consultations and other tools to help protect and improve the health of Canadians. On this page Engaging…

Regulating health products - Canada.ca

Health CanadaCaptures 32Latest capture Apr 11, 2026en

Regulating health products Learn how Health Canada makes sure that the health products you use are safe, effective and of high quality. On this page Approving health products Monitoring safety and quality Creating policies and setting standards Promoting and enforcing compliance…

Draft Guidance Document - Licensing Requirements for Implantable Medical Devices Manufactured by 3D Printing This guidance document is being distributed for comment purposes only. Draft date: 2018/10/08 Health Canada is responsible for helping Canadians maintain and improve their…

Notice: Release of the Draft Guidance Document: Licensing Requirements for Implantable Medical Devices Manufactured by 3D Printing November 8, 2018 Our file number: 18-112090-571 The Draft Guidance Document: Licensing Requirements for Implantable Medical Devices Manufactured by…

Draft Guidance Document - Pre-market Requirements for Medical Device Cybersecurity Download the alternative format Organization: Health Canada Published: 2018-12-07 This guidance document is being distributed for comment purposes only. Draft date: 2018/12/07 Foreword Guidance…

Consultation Notice for Draft Guidance Document – Pre-market Requirements for Medical Device Cybersecurity December 7, 2018 Our file number: 18-119254-906 Health Canada is pleased to announce the release of the Draft Guidance Document Pre-market Requirements for Medical Device…

Consultation: Pre-market Requirements for Medical Device Cybersecurity From Health Canada Current status: Open Opened on December 7, 2018 and will close to new input on February 5, 2019. The purpose of the consultation is to seek stakeholder feedback on the technical…

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