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عربي
About SFDA
About SFDA
نظرة عامة
Authority Establishment
Authority Membership
Authority Activities
Authority Management
Board of directors
SFDA in vision 2030
Vision Realization Office
National Transformation Program
Health Sector Transformation Program
National Industrial Development and Logistics Program
Authority Strategy
Strategy
Authority Values
Annual Reports
Career and Life
Life in SFDA
Career General Goals
Information Lists
All
The Authority
Food
Drugs
Medical Devices
الأعلاف
Pesticides
Laboratories
Cosmetics
Tobacco
Halal
Nutrition
Areas
All
The Authority
Food
Drugs
Medical Devices
الأعلاف
Pesticides
Laboratories
Cosmetics
Tobacco
Halal
Nutrition
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Guidelines
forms
Circulars
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What is a Field Safety Notice?
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What is required of the authorised representative in the event that the distributor (s) do not respond to him / her regarding the implementing of Field Safety Corrective Action?
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How can I update the beneficiary information after completing the registration and approval processes?
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How can I apply for an application to import, re-export or transfer a medical radioactive material?
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How can I communicate with those in charge of MRMR system?
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What are the medical radioactive materials that can be ordered through the electronic system?
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Can the amount of radioactive materials entered into the electronic system be exceeded?
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When submitting an import or re-export request through the company, the name of the medical facility, radioactive material or manufacturer does not appear in the list?
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What is the process to submit a request for being service provider of Quality Assurance and Radiation measurements?
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What is the Validity of Quality Assurance and radiation measurements service provider license?
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