Mandatory Reporting of Serious Adverse Drug Reactions and Medical Device Incidents by Health Care Institutions
Description
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.
Resources
| Name |
Format |
Description |
Link |
| Mandatory Reporting of Serious Adverse Drug Reactions and Medical Device Incidents by Health Care Institutions |
HTML |
|
https://www.canada.ca/en/health-canada/programs/consultation-reporting-serious-adverse-drug-reactions-medical-device-incidents.html |
| Mandatory Reporting of Serious Adverse Drug Reactions and Medical Device Incidents by Health Care Institutions |
HTML |
|
https://www.canada.ca/fr/sante-canada/programmes/consultation-declaration-obligatoire-reactions-indesirable-graves-medicament-instrument-medicaux.html |