Standards › Standard 31 › Forms
Form · DEN-FRM-008 · Version 1.0 · Approved by the ASF Expert Committee
Supports: 31.21
Purpose
Records the specification and material for each laboratory item, the laboratory used and the disinfection before fitting.
How to complete
- Write the specification and material on the order.
- Record the approved laboratory used.
- Record the disinfection before fitting.
Checks
| Check | Entry |
|---|---|
| Patient and order date | Yes |
| Specification and material | Yes |
| Laboratory used (approved) | Yes |
| Disinfection before fitting (date) | Yes |
Evidence
| Reference | Note |
|---|---|
| E-009 | Based on the CDC guidelines for infection control in dental health-care settings (Kohn et al., 2003), ISO 17665 for moist-heat sterilisation, the Minamata Convention on Mercury (2013), IAEA Specific Safety Guide SSG-46 (2018), Council Directive 2013/59/Euratom, and the ADA guidelines on sedation (2016). |
| 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)