Important Update from SFDA – NCMDR: Manufacturer Response Timeframe

The Saudi Food and Drug Authority (SFDA) – National Center for Medical Devices Reporting (NCMDR) has revised the time frame for manufacturers to respond and provide necessary documents related to recalls and adverse events in Saudi Arabia. The SFDA is now enforcing stricter measures to address delays, including timely responses, document submission, and requested information. Click on this link to view the document translsated to English By MRG.