Mandatory Reporting of Serious Adverse Drug Reactions and Medical Device Incidents by Health Care Institutions (French, HTML)

View metadata and access the original French HTML file: Mandatory Reporting of Serious Adverse Drug Reactions and Medical Device Incidents by Health Care Institutions.

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HTML
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Publisher-reported update
2022-10-21

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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French
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