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Open datasets
- Notice: Consultation for proposed amendments to the Medical Device Regulations
- Updates to list of medical devices for mandatory shortage reporting: Notice
- Risk classification guide for medical device establishment inspections GUI-0079
- How Health Canada inspects medical device establishments: Overview
- How Health Canada inspects medical device establishments: About inspections
- How Health Canada inspects medical device establishments: Assessing compliance with the Food and Drugs Act
- How Health Canada inspects medical device establishments: Assessing compliance with the Medical Devices Regulations
- Cancellation of MDELs for failure to pay fees
- Health Canada updates list of medical devices for mandatory reporting of shortages
- Health Canada is modernizing and transforming the Medical Devices Compliance Program
- New labelling and MDEL requirements for medical devices authorized under interim orders on September 1, 2021
- Guidance on Medical Device Establishment Licensing (GUI-0016) - Summary
- Guidance on Medical Device Establishment Licensing (GUI-0016)
- Fees for the Review of Medical Device Establishment Licence Applications
- Fees for the Review of Medical Device Establishment Licence Applications
- Forward Regulatory Plan 2022-2024: Modernizing the Medical Device Establishment Licensing (MDEL) Framework
- Process Validation: Form-Fill-Seal for Drugs (GUI-0008)
- 2017 report on compliance monitoring: Good manufacturing practices for natural health products
- Appearance before the Standing Committee on Public Accounts (PACP) – Report 2, Greening Government Strategy, of the 2022 Reports 1 To 5 of the Commissioner of the Environment and Sustainable Development– 28 October 2022
- Annex 11 to the good manufacturing practices guide: Computerized Systems: GUI-0050
- Annex 7 to the Good manufacturing practices guide for drug products - Selected non-prescription drugs
- Canada and EU recognize good manufacturing practices extra-jurisdictional inspection outcomes before April 1, 2021
- Notice of publication: Good manufacturing practices guidelines for active pharmaceutical ingredients
- Good manufacturing practices guidelines for active pharmaceutical ingredients (GUI-0104) - Summary
- Drug quality and supply chain requirements in light of Russia's invasion of Ukraine
- Changes to policy on drug good manufacturing practices and DEL enforcement (POL-0004)
- 2018-2019 Compliance monitoring project: Good manufacturing practices for natural health products
- Annex 3B to the Good manufacturing practices guide – Positron-emitting radiopharmaceuticals
- Mutual Recognition Agreement Evaluation Guide of Good Manufacturing Practices Compliance Programs
- Drug shortages in Canada: Information for health care providers
- Drug shortages in Canada: Information for industry
- Drug shortages in Canada: Multi-stakeholder steering committee
- Drug shortages in Canada: Regulations and guidance
- Guide to validation – drugs and supporting activities (GUI-0029)
- Guide to validation – drugs and supporting activities (GUI-0029) - Summary
- Health products compliance: International agreements and collaboration activities
- Good Manufacturing Practices (GMP) - Inspection Summary Reports
- The Historic Village of Waterdown
- Waste Diversion Rates Monthly Totals
- Struggle & Survival
- Building Division celebrates 75 years
- Tax Impact
- Parking Restrictions on Through Streets
- Child and Youth Health Atlas
- Art Bank Collection
- Percentage of workforce anticipated to work on-site or remotely over the next three months, first quarter of 2023
- Challenges faced when adopting or incorporating technologies, first quarter of 2023
- Plans to implement new or update pre-existing digital technology to enable or enhance other business processes, first quarter of 2023
- Plans to implement new or update pre-existing digital technology to enable or enhance e-commerce or online sales, first quarter of 2023
- Ability for the business or organization to take on more debt, first quarter of 2023