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Remaining Shelf Life Requirement for Imported Medicines – Qatar

Qatar MoPH Issues Circular on Remaining Shelf Life Requirement for Imported Medicines

SFDA Issues “Guidelines for Chemical and Pharmaceutical Quality Documentation of Small Molecules Investigational Products in Clinical Trials” (Version 1.0)

Saudi Food and Drug Authority (SFDA) has issued Version 1.0 of new

SFDA Issues Updated Guidance on “Combination Products Classification and Registration” (Version 2.0)

SFDA has issued Version 2.0 of the “Guidance for Combination Products Classification

SFDA – “Products Classification Guidance” V 9.0

SFDA has issued Version 9.0 of the “Products Classification Guidance”, introducing updated

SFDA- “Clinical Considerations for Vaccines” V 2.0

SFDA issued the updated “Clinical Considerations for Vaccines” guideline – Version 2.0

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

SFDA- “Verification & Abridged Pathways” Guideline updates

SFDA issues updated “Verification & Abridged Pathways” Guideline (Version 3.0 — Issued

SFDA- Approach of Dealing with Patents When Registering Generic Drugs in SFDA Guideline

The Saudi Food & Drug Authority (“SFDA”) has issued a new guidance

Regulinked
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

Regulinked
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”

Regulinked
October 9, 2025
Guideline
No Comments

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Category: Human