Frequently Asked Questions (FAQs)
Welcome to the FAQs section of the National Medicines Regulatory Authority (NMRA), Somalia. Below are answers to commonly asked questions regarding our regulatory processes and services.
What are NMRA’s main functions?
NMRA is responsible for:
✔ Registering pharmaceutical products for market authorization.
✔ Licensing pharmacies, wholesalers, and manufacturers.
✔ Conducting market surveillance and pharmacovigilance.
✔ Regulating medicine imports and distribution.
✔ Ensuring compliance with national and international health regulations.
How do I register a pharmaceutical product in Somalia?
To register a product, you must submit a Product Registration Application through the NMRA online portal or in person, including necessary documentation such as quality, safety, and efficacy data.
How long does the product registration process take?
The registration timeline varies based on product type and regulatory requirements but typically takes several weeks to months after a complete application is submitted.
Can I sell or distribute a medicine without NMRA approval?
No. All medicines must be registered and approved by NMRA before they can be legally sold or distributed in Somalia.
