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NHRA updated “Medicine Submission, Renewal & Variations Guidelines”

NHRA has updated three key pharmaceutical regulatory guidelines in Bahrain as part

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

Kuwait MOH – “Requirements for registration of Herbal products”

The Ministry of Health (MOH) – Kuwait has issued Ministerial Decree No.

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January 24, 2026
Guideline
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Kuwait MOH – “Requirements for registration of Medical Devices & IVD”

The Ministry of Health (MOH) – Kuwait has issued Ministerial Decree No.

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January 24, 2026
Guideline
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Kuwait MOH – “Requirements for cosmetic and personal care products”

The Ministry of Health (MOH) – Kuwait has issued Ministerial Decree No.

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January 23, 2026
Guideline
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Kuwait MOH – “REGULATORY FRAMEWORK FOR DRUG APPROVAL”

The Ministry of Health (MOH) – Kuwait has issued Ministerial Decree No.

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January 23, 2026
Guideline
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Kuwait MOH – “Content of the Registration Dossier for human pharmaceutical medicinal products”

The Ministry of Health (MOH) – Kuwait has issued Ministerial Decree No.

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January 23, 2026
Guideline
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NHRA – “Alternative and Complementary Medicines Guideline” (V 1.2)

NHRA issues updated “Alternative and Complementary Medicines Guideline” (V 1.2) 🔍 What’s

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November 22, 2025
Guideline
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NHRA – issues updated “Health Products Licensing Guideline” V 3

NHRA issues updated “Health Products Licensing Guideline” (V 3.0) 🔍 What’s new:

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November 22, 2025
Guideline
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NHRA – issues updated “Medicine Licensing Guideline” V 4.1

NHRA issues updated “Medicine Licensing Guideline” (Version 4.1) 🔍 What’s new:

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November 13, 2025
Guideline
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