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"If the authorised representative of a manufacturer has a authorised representation certificate for devices classified with a specific classification, but the device affected by the Field Safety Corrective Action is not from the production line responsible for it even though it is of the same classification, is he responsible for closing the Field Safety Corrective Action for this device? " FAQ

Investor Guide to Obtain Scientific Office Licensing Regulations

Is it allowed to combine and add more than a medical device or products in one medical device marketing authorization? FAQ

what is In-Vitro Medical Device definition FAQ

"SFDA" Warns of Using Two Keratin Hair Treatment Products as They Contain High Percentage of "Formaldehyde" Warnings

CEO of SFDA Visits Food Facilities in Makkah Region News

SFDA CEO Reviews the Authority's Readiness to Serve Pilgrims and Inspects Facilities in Makkah News

SFDA Grants Breakthrough Designation to Prevent and Reduce Bleeding Episodes in Patients with Hemophilia A News

Biotechnology and Innovation in Medical Devices industry Workshop

UPDATES: A prospective non-interventional study investigating the treatment effect of Tresiba® in adult patients with type 2 diabetes in Saudi Arabia Drug Clinical Trial