Mandatory Reporting of Serious Adverse Drug Reactions and Medical Device Incidents by Health Care Institutions

Reports about serious ADRs and MDIs can be important signals of emerging safety issues. Such post-market observations can also lead to improved safety information about a product.

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Title (French) Déclaration obligatoire des réactions indésirables graves à un médicament et des incidents relatifs aux instruments médicaux par les établissements de soins de santé
Update Frequency as_needed
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Sensitivity Level unrestricted
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Open Canada Date Published 2020-01-28 00:00:00
Open Canada Date Modified
Open Canada Subject ["health_and_safety"]
Open Canada Keywords {"fr": ["rapports sur les effets indésirables graves", "rapports sur les inhalateurs à doseur graves", "problèmes de sécurité émergents", "observations post-commercialisation", "amélioration des informations sur la sécurité", "déclaration des effets indésirables", "déclaration obligatoire des effets indésirables"], "en": ["reports about serious-ADRs", "reports about serious-MDIs", "emerging safety issues", "post-market observations", "improved safety information", "adverse-reaction reporting", "mandatory adverse-reaction reporting"]}
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