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عربي
Hajj And Omrah
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
Laws and Regulations
Guidelines
forms
Circulars
FAQ
Laws and Regulations
Guidelines
forms
Circulars
FAQ
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FAQ
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“SFDA” Warns Against 3 Spices due to Illegal Use of Banned Dyes
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CEO of SFDA Visits Food Facilities in Makkah Region
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"SFDA": companies that do not comply with the inclusion of cosmetic products will considered as violation
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DA Detects 571 Unlicensed Facilities During Hajj Season
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"How medical devices classification must be performed"
FAQ
What are the fees of marketing authorization application and how long does it take to issue?
FAQ
Is it allowed to combine and add more than a medical device or products in one medical device marketing authorization?
FAQ
What is Unique Device Identification (UDI) for Medical Devices?
FAQ
What are the required documents that need to be submitted to obtain the medical devices Marketing Authorization Certificate through the Technical File assessment (TFA) track?
FAQ
What does mean, “The timeframe for returned MDMA application is 60 calendar days” in announcement (8) 8/2019?
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