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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

Gulf Axis Contracting Establishment service providing facilities

Minister of Health Visits SFDA's Hajj Operations Center and Inspects Service Readiness News

The British Ambassador Visits SFDA News

An observational disease and clinical outcomes registry of patients with acid lipase (LAL) deficiency Drug Clinical Trial

Vitamin D Status Correction and Validation of its Potential Clinical Utility through Discovery Proteomic Analysis Drug Clinical Trial

An Observational Registry of Abatacept in Patients with Juvenile Idiopathic Arthritis Drug Clinical Trial

A prospective Randomized study of General Anesthesia versus Anesthetist Administered sedation for ERCP Drug Clinical Trial

The Multi-National Gilenya Pregnancy Exposure Registry in Multiple Sclerosis Drug Clinical Trial

A randomised blinded placebo controlled trial of hydrocortisone in critically illpatients with septic shock Drug Clinical Trial