Description

Pharmaceutical agents and representatives may submit a request to the Registration and Drug Pricing Section of the Pharmacy and Drug Control Department (PDCD) to register herbal manufacturer.

Online Instructions

• Log in to the Pharmacy and Drug Control System.
• Select “Registration of Herbal Manufacturer” service and enter all the required information.
• Attach the following documents:

• Filled in Registration of Herbal Manufacturer form
• Cover letter stamped by the agent and signed by the company authorized person.
• Valid legalized original manufacturing license certificate, issued by the competent health authorities in the country of origin
• Valid legalized original Good Manufacturing Practice (GMP) certificate, issued by an authoritative health government body in the country of origin
• Original legalized letter from the manufacturing company clarifying the relation with the Marketing Authorization Holder (MAH) and the names of products manufactured for its interest
• List of products manufactured in the same site on sale in the country of origin issued by the manufacturer with supporting documents, namely copies of the registration certificate of such products
• Copy of registration certificates of manufacturing site in GCC countries or other countries

• Submit your application.

Fees

No fees are required for this service.