MoHAP / EDE product registration in the UAE
Medicines, medical devices, and capsule/pressed-form supplements route through the federal pathway (Ministry of Health and Prevention / Emirates Drug Establishment), not Dubai Municipality Montaji.
Documents this route requires
- Federal application via MoHAP/EDE (or through a licensed bench partner)
- GMP and free-sale evidence from the country of manufacture
- Full composition and clinical/supporting dossier
Label requirements
- Federal label rules: Arabic primary panel, registration number, batch and expiry
Watch-outs
- The federal route runs in months, not weeks, and needs a licensed local partner or importer of record.
We handle this for you
Product Registration Assistance · from AED 1,490
View the serviceFrequently asked questions
Do medical and pharmaceutical products need product registration in the UAE?
Medicines, medical devices, and capsule/pressed-form supplements route through the federal pathway (Ministry of Health and Prevention / Emirates Drug Establishment), not Dubai Municipality Montaji.
Which documents does this route require?
The filing checklist for this route: Federal application via MoHAP/EDE (or through a licensed bench partner); GMP and free-sale evidence from the country of manufacture; Full composition and clinical/supporting dossier.
What does it cost?
from AED 1,490 per product (cosmetics & personal care); supplements from AED 2,900 , government and lab fees excluded
How long does the process take?
Our engagement timeline for this route: Depends on product category , confirmed after scoping.
This page reflects our classification engine; your consultant confirms the route with you before any filing.