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Regulation of Medical Devices
The article focused on the efforts of the Saudi Food and Drug Authority (SFDA) during 2025 to enhance oversight of medical and food products. The initiatives included issuing 22 regulatory decisions to address safety issues, targeting more than 30.8 million medical devices, as well as expanding and updating field inspection tools. Additionally, new systems were adopted for employees and facilities, and laboratories were upgraded using modern technologies such as artificial intelligence. The Authority also launched a platform for uploading test results and compliance data. It issued warnings against the use of diesel in manufacturing processes, reflecting a shift towards a more proactive and transparent regulatory model, with the goal of elevating product safety and protecting consumers.
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