Mandatory reporting of serious adverse drug reactions and medical device incidents by hospitals - Guidance document

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This is a public health concern resulting in significant costs to the health care system as well as individual impacts on Canadians. Health Canada's monitoring of therapeutic product safety plays a vital role in public health and patient safety, providing health care providers and patients with the most up-to-date knowledge for decision making. It also provides Health Canada with information needed to monitor the benefit-risk ratio of products and act to protect Canadians where appropriate.

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Mandatory reporting of serious adverse drug reactions and medical device incidents by hospitals - Guidance document HTML https://www.canada.ca/en/health-canada/services/drugs-health-products/medeffect-canada/adverse-reaction-reporting/mandatory-hospital-reporting/drugs-devices/guidance.html
Mandatory reporting of serious adverse drug reactions and medical device incidents by hospitals - Guidance document HTML https://www.canada.ca/fr/sante-canada/services/medicaments-produits-sante/medeffet-canada/declaration-effets-indesirables/declaration-obligatoire-hopitaux/medicaments-instruments/orientation.html

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