Mandatory Reporting of Serious Adverse Drug Reactions and Medical Device Incidents by Health Care Institutions (English, HTML)
View metadata and access the original English HTML file: Mandatory Reporting of Serious Adverse Drug Reactions and Medical Device Incidents by Health Care Institutions.
- Format
- HTML
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- file-only
- 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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- Formats
- HTML
- File languages
- English
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- Access original file