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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
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Pesticides
Laboratories
Cosmetics
Tobacco
Halal
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Implantable cardioverter defibrillator (ICD) REGISTRY
Clinical Trial
Intelligent Autism Screening Chatbot with Multimodal Interaction Across CHAT Variants
Clinical Trial
Evaluation of EQUIA Forte® HT as a restorative material for primary molars and in vitro evaluation of the effect of different surface coating agents on its water sorption, solubility and hardness
Clinical Trial
Basirah: An AI-Powered Digital Therapy Platform for Autism Spectrum Disorder Across Ministry of Defense Healthcare Services
Clinical Trial
Guidance on MDMA –Significant and Non-Significant Changes (MDS-G012)
Regulations
(SG-1902-08-H) Allergan Textured Breast Implants and Tissue Expanders.
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A Phase 3, Randomized, Open-label Study to Evaluate the Efficacy and Safety of sac-TMT (Sacituzumab Tirumotecan, MK-2870) Followed by Carboplatin/Paclitaxel vs Chemotherapy, Both in Combination with Pembrolizumab as Neoadjuvant Therapy for High-Risk, Early-Stage, Triple-Negative Breast Cancer or Hormone Receptor-low Positive/Human Epidermal Growth Factor Receptor-2 Negative Breast Cancer.
Drug Clinical Trial
An open-label, controlled, multi-site, Phase 2 clinical trial to assess the ureagenesis capacity in newborns and infants up to the age of 12 months with neonatal and infantile onset of urea cycle disorders (UCD) using a 15N ammonium chloride tracer compared to newborns and infants without UCD
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Saudi Food and Drug Authority is publishing an announcement about Blood Glucose Meters Model CLEVER CHEK TD-4232
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CEO of SFDA Discusses “Regulatory Pathways: Balancing Innovation and Safety” at the Global Healthspan Summit 2025
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