Substandard and falsified medical products (SFMPs) – questions to consider when assessing risk
23 July 2025
| Technical document
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Overview
This document is supplementary material to the SFMP trainer’s toolkit and must be used in conjunction with the document, Prioritization and Risk Parameters (section 5.1.5 of SFMP trainer’s toolkit).
WHO Team
Incidents and SF (ISF)
Number of pages
3