Kuwait MOH – “REGULATORY FRAMEWORK FOR DRUG APPROVAL”
The Ministry of Health (MOH) – Kuwait has issued Ministerial Decree No.
Regulinked
- January 23, 2026
- Guideline
- No Comments
Tag: eCTD
Kuwait MOH – “Content of the Registration Dossier for human pharmaceutical medicinal products”
The Ministry of Health (MOH) – Kuwait has issued Ministerial Decree No.
- January 23, 2026
- 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
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
ReguLinked Consulting helps pharmaceutical, healthcare, and life sciences companies achieve seamless market access and regulatory compliance across Saudi Arabia and the GCC. Trusted expertise. Local insight. Real results.