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Code Procedures of Importing and Exporting Regulations

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

Feed Establishments License Eservices

A Guide to Fresh Fruit and Vegetable Registration and Licensing Regulations

Zoledronic acid Fresenius Kabi(Zoledronic acid) Risk Minimization Activity

Benzodiazepines Risk Minimization Activity

SFDA Participates in the Optimal Use of Antimicrobial Drug for Animal Health Conference News

SFDA: "Cepagon Pills" Weakens the Perception and Causes Serious Side Effects News

Product Verification and Validation Requirements for Medical Devices Workshop