Standards › Standard 41 › Registers and logs
Register · TRM-REG-003 · Version 1.0 · Approved by the ASF Expert Committee
Supports: 41.5
Purpose
Records each adverse event from treatment or a product, its review, and any change in practice it leads to.
How to complete
- Record each adverse event when it is reported.
- Record its review.
- Record any pattern found and the change made.
Checks
| Check | Entry |
|---|---|
| Event, date and product or treatment | Yes |
| Review date and reviewer | Yes |
| Pattern found (yes or no) | Yes |
| Change in practice and date | Yes |
Evidence
| Reference | Note |
|---|---|
| E-009 | Based on the WHO Traditional Medicine Strategy 2014–2023, the WHO guidance on substandard and falsified medical products, and the ASF Hospital standard for informed consent and incident reporting. |
| E-006 | ASF Policy Framework v1.2. Adapted. |
| E-009 | ASF Expert Committee consensus. |
Change history
| Version | Date | What changed | Approval |
|---|---|---|---|
| 1.0 | the date of approval | First version | set Expert Committee approval |
E-learning for this document
References
- Accréditation Sans Frontières (2026). ASF Policy Framework v1.2. (E-006)
- Accréditation Sans Frontières (2026). ASF Expert Committee consensus on Standard 1. (E-009)