SFDA- “Guideline on Requirements for Advertising and Promotion of Pharmaceutical and Herbal Products” V 7.0
The Saudi Food & Drug Authority (“SFDA”) has issued V 7.0 of
Regulinked
- January 27, 2026
- Guideline
- No Comments
Tag: Human Drug
NHRA – issues updated “Medicine Renewal Guideline” V 2.1 & “Medicine Variations Guideline” V 3.1
NHRA issues updated “Medicine Renewal Guideline” (Version 2.1) & “Medicine Variations Guideline”
- November 13, 2025
- Guideline
- No Comments
CMC Guidance for Human Gene Therapy Clinical Trial Applications
SFDA Issues Final CMC Guidance for Human Gene Therapy Clinical Trial Applications.
- November 7, 2025
- Consulting
- No Comments
SFDA- “Verification & Abridged Pathways” Guideline updates
SFDA issues updated “Verification & Abridged Pathways” Guideline (Version 3.0 — Issued
- October 31, 2025
- Acceleration process
- No Comments
SFDA- Approach of Dealing with Patents When Registering Generic Drugs in SFDA Guideline
The Saudi Food & Drug Authority (“SFDA”) has issued a new guidance
- October 23, 2025
- Guideline
- No Comments
Oman MOH – Mandatory Renewal of Pharmaceutical Licenses via the Electronic Health Portal (EHP)
OMAN MOH issued new Circular No. 194/2025 – Mandatory Renewal of Pharmaceutical
- October 14, 2025
- Guideline
- No Comments
Guideline on the Preparation & Submission of eCTD Dossiers – Kuwait
Kuwait MoH issues “Guideline on the Preparation & Submission of eCTD Dossiers”
- October 9, 2025
- Guideline
- No Comments
Braille Requirements for Labeling Information – Qatar
Qatar MOPH issues new Guideline on Braille Requirements for Labeling Information of
- October 9, 2025
- Guideline
- No Comments
SFDA issues “Good Review Practices (GRevPs)” Guideline Version 1.0
SFDA issues “Good Review Practices (GRevPs)” Guideline Version 1.0 🔍 What’s new:
- October 3, 2025
- Guideline
- No Comments
SFDA updates – Guideline of Data Requirements for Human Drug Submissions – Version 4.0
SFDA publishes Version 4.0 of Data Requirements for Human Drug Submissions (August
- September 14, 2025
- Guideline
- No Comments
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