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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
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Halal
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Randomized, four-way, four-period, single oral dose, open-label, crossover, bioequivalence study to compare Tacrolimus Immediate-release capsules (5 mg tacrolimus) versus Prograf® Immediate-release capsules (5 mg tacrolimus), in healthy subjects under fasting conditions.
Drug Clinical Trial
A Randomized, Double-Blind, Placebo Controlled Cross- Over Study toInvestigate the Efficacy and Safety of SC0023, a Magnesium Salt Oral SprayDevice, in Adults with Refractory or Unexplained Chronic Cough
Clinical Trial
SFDA Warns Against Using the Batch Number (MC1605) of "Biotrue Multi-Purpose Solution" as it is Possible to Lead to Conjunctivitis
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A Phase 3, Prospective, Multicenter, Double-blind, Double-dummy, Randomized, Active controlled, Parallel-group, Group-sequential, Adaptive, Event-driven Study to Compare Efficacy, Safety, and Tolerability of Macitentan 75 mg Versus Macitentan 10 mg in Patients with Pulmonary Arterial Hypertension, Followed by an Open-label Treatment Period With Macitentan 75 mg. (UNISUS)
Drug Clinical Trial
Requirements for Advertisement Approval and Launching Awareness and Charity Campaigns for Medical devices (MDS-REQ8)
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(SG-2003-194-H) potential for the unintended use of the Device may harm the patient
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Requirements for Unique Device Identification (UDI) for Medical Devices (MDS – REQ 7)
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Clinical Performance Study of SARS-CoV-2 Virus Antigen Detection Kit (Immunofluorescence Chromatography)
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The SFDA Will Sponsor One of The Panel Discussions:The 4th Conference on Food and Nutrition Takes Place Next Sunday
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Early administration of Tocilizumab in Immunocompromised and potential high-risk patients for developing COVID-19
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