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The Implementing Regulations of the Law of Pharmaceutical and Herbal Establishments and Products

2020-12-28
The Implementing Regulations of the Law of Pharmaceutical and Herbal Establishments and Products
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The SFDA Grants Breakthrough Designation to Atrasentan (Vanrafia) for Primary Immunoglobulin A (IgA) Nephropathy

2025-05-13

Treatment

The Saudi Food and Drug Authority (SFDA) has granted Breakthrough Designation to Novartis's medication Atrasentan (Vanrafia) , which is indicated to reduce proteinuria in adults with primary immunoglobulin A nephropathy (IgAN) who are at risk of disease progression.

A Selective Endothelin (A) Receptor Antagonist

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Regulatory Guidance for Literature Based Support for Efficacy and Safety of Medicine

2025-05-12
Regulatory Guidance for Literature Based Support for Efficacy and Safety of Medicine
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The SFDA Grants Breakthrough Designation to Qfitlia for Hemophilia A and B

2025-05-10

The Saudi Food and Drug Authority (SFDA) has granted breakthrough designation to Sanofi's medication, Fitusiran (Qfitlia), which is indicated for routine prophylaxis to prevent or reduce the frequency of bleeding episodes in adult and adolescent patients aged 12 years and older with hemophilia A or B, with or without factor VIII or IX inhibitors.

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The SFDA Approves Breakthrough Designation Application for Breast Cancer Therapy “Inluriyo”

2025-05-05

The Saudi Food and Drug Authority (SFDA) has granted Breakthrough Designation to Eli Lilly’s medication, Imlunestrant (Inluriyo), for the treatment of advanced breast cancer. Imlunestrant is being developed as a monotherapy for the treatment of adult patients with estrogen receptor (ER)-positive, human epidermal growth factor receptor 2 (HER2)-negative, estrogen receptor 1 (ESR1)-mutated advanced or metastatic breast cancer who have previously been treated with an endocrine based regimen.

Imlunestrant: A Selective Estrogen Receptor Inhibitor

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The SFDA Approves Clinical Trial for Novel Biologic Therapy for Genetic Propionic Acidemia

2025-05-04

Experimental Treatment by mRNA

The Saudi Food and Drug Authority (SFDA) has approved a clinical study registration titled "A Global Phase 1/2 Open-Label Dose-Optimization Study to Evaluate the Safety and Pharmacokinetics of the Biologic Treatment (mRNA-3927) in Participants with Propionic Acidemia." This research will investigate an innovative experimental therapy utilizing messenger RNA (mRNA) technology to address a rare inherited disorder affecting amino acid metabolism.

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Classifying Legal Status of Veterinary Medicinal Products Guidance

2025-05-04
Classifying Legal Status of Veterinary Medicinal Products Guidance
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The SFDA: Leveraging Modern Technology for Enhanced Hajj Inspection Efficiency

2025-05-03

The Saudi Food and Drug Authority (SFDA) is continuously advancing its regulatory framework and boosting its operational effectiveness. This aligns with the Health Sector Transformation Program, a key pillar of Saudi Vision 2030.

During the Hajj season, the SFDA intensifies its focus on employing technologies to protect pilgrim health and safety by providing top-tier quality control and regulatory services that meet the highest standards.

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Drug Factory License

It is a service that is provided to grant a license to pharmaceutical factory facilities

Service steps

  • Log in to the Ghad Platform.
  • Create an account based on user type.
  • Submit a facility registration application.
  • Pay the fee.
  • Issue the license after approval and review.

Conditions

Active account on the Ghad platform, and environmental permit from the National Center for Environmental Compliance Control

Service requirements

  • A commercial register includes the economic activity related to SFDA's activities.
  • An industrial License.
  • Academic certificates, experience, and professional registration cards for the technical manager and quality control officer. 

Frequently asked questions

- كيف يمكنني الحصول على الرخصة؟

بإمكانكم الحصول على الترخيص من خلال النظام الموحد - غد -

- هل للرخصة تاريخ انتهاء؟

نعم. بحسب ما تم تقديمه وتوضيحه أثناء تقديم طلب الترخيص.

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SFDA Clears the First Medical Shipment of 44 Tons for Hajj Pilgrims

2025-04-26

The Saudi Food and Drug Authority (SFDA) has successfully completed the clearance procedures for the first medical shipment intended for this year's Hajj pilgrims. The shipment arrived via Prince Mohammed bin Abdulaziz International Airport in Medina, weighing 44 tons and consisting of essential medicines and medical products.

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