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As a authorised representative of a manufacturer I did not import the affected devices in the Field Safety Corrective Action , do I have to fill out the form “Statement Confirming Saudi Arabia is Not Affected by FSCA”? FAQ

In the event that the responsible person is not responding / present at the hospital to sign or receive the required document regarding Field Safety Corrective Action, what is the procedure taken for this case? FAQ

"What is the allowed period for submitting a corrective plan to implement Field Safety Corrective Action? " FAQ

"in the risk assessment form mentioned in the Guidance on Medical Device Field Safety Corrective Actions, is it possible to choose more than one option for the same standard?" FAQ

What do we mean by post-marketing evaluation studies? FAQ

What are the expected outcomes of post-marketing evaluation studies? FAQ

Guideline for Submitting a claim Evaluation Request of Health and Nutrition Claims Regulations

Application for Health and Nutrition Claim Evaluation Form Forms

SFDA Announces New Protocol for the Approval of Health & Nutrition Claims not Covered by National Standards News

(SG-2012-288-H) potential for electrode body fracture Medical Report