Report of existing technologies used to screen and detect substandard and falsified medical products

Overview

Regulatory authorities are responsible for overseeing medical products and are tasked with the prevention, detection, and response to substandard and falsified medical products. Ministries of health and other stakeholders that are involved in procurement of medical products, such as non-governmental organizations, academia, and procurement agencies, play equally crucial roles, alongside regulatory authorities, in implementing interventions to address substandard and falsified medical products.