Common mistakes in registering Low-Risk Medical Devices
Common mistakes in registering Low-Risk Medical Devices Saudi DoC: It must be…
Updates on the Compliance Timeframe for the Requirements of Medical Devices unique device Identification (Saudi-DI)
Update on the compliance timeframe for the requirements of medical devices…
Webinars for Drug and Medical Device Specialists on the Efforts to Address the Outbreak of "COVID-19"
The Saudi Food and Drug Authority (SFDA) organizes awareness webinars and…