The entire product related documents only then the official fee has to be submitted along with the application. The application is first checked by the Technical team before forwarded to the Ministerial Committee for final decision. Further follow up needs to be carried out from a Pharmacological Analysis Section of at the Drug Department and other requirements have to be submitted through E-services. Once the Technical committee has a thorough examination of the products again and approves registration.
Product registration is required to import any medical or pharmaceutical-related products and devices in the UAE, the product registration needs to be done at MOHAP regardless of the emirates the drug store is located
Depends on the product type the registration process and required supporting documents may vary, talk to our consultant to get more information for the product type you are planning to register.
No, it is mandatory only MOHAP licensed pharmaceutical warehouses can only register the product under their license and handle the all post-market obligations.