Catalogue - Canadian Urban Data Catalogue (CUDC)

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Catalogue Entry: President of the PHAC before the Standing Committee on Health: Canadian...

Briefing packages for President, Minister and Deputy Ministers’ Parliamentary Committee appearances.
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Catalogue Entry: Standing Committee on Health

Briefing packages for President, Minister and Deputy Ministers’ Parliamentary Committee appearances. President of the PHAC before the Standing Committee on Health: Canadian...
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Catalogue Entry: Resources for Canadians living with pain during COVID-19: Resources

The Government of Canada and the Canadian Pain Task Force (CPTF) recognize Canadians living with chronic pain need additional supports during COVID-19. The following list of...
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Catalogue Entry: Conducting a clinical trial for COVID-19 medical devices: List of authorized...

The table below lists the clinical trials authorized by Health Canada for COVID-19-related medical devices.
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Catalogue Entry: Collaboration with the Public Health Agency of Canada’s National Microbiology Lab

The Public Health Agency of Canada’s National Microbiology Lab (PHAC-NML) will conduct independent scientific laboratory evaluation of some COVID-19 testing devices when...
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Catalogue Entry: Health Canada’s regulatory response to COVID-19: Access to health products

Health Canada introduced innovative and agile regulatory measures. These measures expedite the regulatory review of COVID-19 health products without compromising safety,...
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Catalogue Entry: Health products that make false or misleading claims to prevent, treat or...

Health Canada is warning Canadians about the risks of purchasing health products that make unauthorized claims to prevent, treat or cure COVID-19.
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Catalogue Entry: Good Manufacturing Practices and COVID-19

Good manufacturing practices (GMP) ensure that drugs meet the quality standards appropriate to their intended use before they are sold.
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Catalogue Entry: Drug establishment licences and COVID-19

All Canadian drug establishments must have a drug establishment licence to fabricate, package/label, distribute, import, wholesale or test a drug as required under Part C,...
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Catalogue Entry: Regulatory considerations on the classification of non-medical masks or face...

This notice explains under which circumstances non-medical masks or face coverings would be subject to the regulatory framework for medical devices during the COVID-19 pandemic.
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Catalogue Entry: Canada's Drug Supply Chain

The Canadian drug supply chain is complex, with distinct roles and responsibilities among many players including manufacturers, wholesalers, hospitals, health care practitioners...
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Catalogue Entry: Causes of Drug Shortages in Canada

Drug shortages can occur for any number of reasons and can result from problems at any point in the drug supply chain.
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Catalogue Entry: Regulatory decision summaries of drugs and health products

Understand the decisions to approve or not approve the sale of drugs and medical devices in Canada.
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Catalogue Entry: Drug and Health Product Submissions Under Review (SUR)

Present the list of new drug submissions (NDSs) that are currently being reviewed.
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Catalogue Entry: Submission 'Class'

For eligible submissions accepted into review on or after October 1, 2018, the submission 'class' added to the Lists of submissions currently under review.
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Catalogue Entry: Generic submissions under review

How to access a list of generic drug submissions currently under review.
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Catalogue Entry: How Drugs are Reviewed in Canada

Health Canada's drug products fact sheet describes how drugs are reviewed in Canada including how drugs are developed and submitted for authorization to conduct clinical trial.
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Catalogue Entry: Guidance on Drug Establishment Licences (GUI-0002)

These guidelines are meant to help companies in the drug manufacturing industry and health care professionals understand how to comply with regulations, specifically drug...
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Catalogue Entry: Service Standard for the Right to Sell Drugs under the Food and Drug Regulations

Before a drug is authorized for sale in Canada, it must be issued a DIN in accordance with the Food and Drug Regulations. Also in accordance with the Food and Drug Regulations,...
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Catalogue Entry: Clinical information on drugs and health products

Drug and medical device manufacturers submit clinical information to Health Canada for the approval of new products. Health Canada assesses this clinical information to reach a...
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2,962 catalogue entries found