The Ministry of Health (MOH) – Kuwait has issued Ministerial Decree No. (342) of 2025, establishing the Regulatory Framework for Drug Approval for human medicinal products in Kuwait.
The document provides a comprehensive framework governing review pathways, approval processes, timelines, and post-approval obligations.
🔍 What’s new:
- Establishes a formal regulatory framework defining all drug review pathways applicable in Kuwait.
- Defines eight review pathways, including standard, fast track, priority, expedited, biosimilar, emergency use, rolling, and GHC-approved drug pathways, each with specific eligibility criteria and timelines.
- Introduces clearly defined assessment timelines, response cycles, and clock-stop mechanisms for each pathway.
- Formalizes approval types, including standard approval, conditional approval, and Emergency Use Authorization (EUA), with defined validity periods.
- Specifies post-approval obligations, renewal requirements, pricing considerations, and conditions for transition from conditional or emergency approvals to standard registration.
💡 Why it matters:
- Provides regulatory clarity on how and when different drug categories can access the Kuwait market.
- Enhances predictability for applicants by defining pathway-specific timelines, obligations, and approval validity.
- Supports structured decision-making for products addressing serious, life-threatening conditions or unmet medical needs.
📌 How ReguLinked can support you:
- Support pathway selection based on product profile and eligibility criteria.
- Assist with regulatory strategy planning for standard, accelerated, or emergency pathways.
- Support review of submission readiness, timelines, and post-approval obligations under MD No. 342/2025.
📎 Official PDF: Framework for human Drug Approval – Kuwait
📨 Planning to Submit New, Renewal or Variation application in Kuwait?
Let ReguLinked accelerate your submissions with a fully compliant with Kuwait requirements and strategy.
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