Standard 8.10 requires SARSS report forms to be available and adverse reactions reported; how will the inspector check this?
Related Questions
- I report adverse drug reactions (ADRs), but another pharmacist reports medication errors. Should we continue collecting data about errors or focus strictly on adverse drug events and patient harm?
- Standard 8.10 requires SARSS report forms to be available and adverse reactions reported; how will the inspector check this?
- How Do You Report Adverse Drug Reactions?
