Search Results

Containing any of the words

Only of the type

What is SFDA procedure if some users do not respond to the Authorized Representative (AR) or the supplier? regarding a Field Safety Corrective Action? FAQ

If the Authorized Representative (AR) was unable to obtain a response to provide the corrective plan or ensure if the Kingdom is not affected within 5 working days, what is required and how is the response? FAQ

Who should fill out the risk evaluation form? The manufacturer or Authorized Representative (AR) and the importer? FAQ

The Saudi Food & Drug Authority Hosts "the Extra-Ordinary Meeting for the Heads of the Food Regulatory Agencies" News

Saudi Drug Registration (SDR) Eservices

(SG-2008-253-H) Advices on Substandard/Falsified medical devices used in the context of the COVID-19 pandemic Medical Report

National Diagnostic Reference Levels Regulations

(SG-2006-239-H) Ventilators in Isolation Rooms May Fail to Alert Clinicians of Critical Alarm Conditions Medical Report

A Phase 3, Open-Label, Single-Arm Trial Evaluating the Safety, Tolerability, and Immunogenicity of 13-valent Pneumococcal Conjugate Vaccine in Children With Sickle Cell Disease Previously Immunized With 23 Valent pneumococcal polysacchride Vaccine. Drug Clinical Trial

Multi-Center Open Label Study to Evaluate the Safety, Tolerability and Efficacy of Tocilizumab in Patients With Active Rheumatoid Arthritis on Background Non-biologic DMARDs Who Have An Inadequate Response to Current Non-Biologic DMARD or Anti-TNF Therapy Drug Clinical Trial