Product Registration
Cosmetic Products Registration Services
- Company or organization must be a list with Dubai Municipality
- Applicant company must fill out the form for each product
- After all the requirements are finalized a registration report of the consumer product is made
Pharmaceutical Products Registration
- The applicant should have a medical store licensed by theMinistry of Health.
- The registration will be valid for five years, after completing the period it must be renewed.
- The product details must be registered with a trade name.
Herbal Product Registration Services
- A copy of the certificate of registration of the manufacturer in the Ministry of Health UAE.
- An Application Form for registering a Herbal product. Except for Agent’s information that is filled-in through the Agent in the UAE.
- A Free Sale Certificate (FSC) or Certificate of Pharmaceutical Product (CPP).
Biological Products Registration
- FURLS (Food and Drug Administration Unified Registration and Listing System) to register and also list your information.
- Registration of a drug should be done by the MOH before you are importing the same inside the United Arab Emirates market (Pharmaceuticals Law 1983)
- According to section 510 of the Federal Food, Drug, as well as Cosmetic Act, except they are exempt under 21 CFR 607.65
Food Supplements Registration
- Food laws are established within the Gulf Cooperation Council (GCC) and Gulf Standardization Organization (GSO) and adopted by the participating member-countries.
- Compilation, Gap analysis, and Submission of Dossier to the Health Authority (HA).
- Food Regulatory Strategy, Label and Claims Review, Formula Review/Ingredients Assessment.
Medical Device Registration
- A summary of “compulsory” reported problems with a device since its introduction in the market
- Risk assessment involving risk analysis, evolution as well as reduction measures
- Complete detailed information on the safety studies that include clinical as well as pre-clinical studies, software studies, software validation studies where proper, and of the published reports dealing with the device