Registration of veterinary products manufacturing company

About the Service

Through this service, approved the registration of foreign veterinary products manufacturers through a licensed warehouse

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Service Process

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Required Documents

1. 1. Provide a file that includes the following basic information: -Type and activity of the company. -Number of factories owned by the company and its addresses.
2. -The company's relationship with each of these factories and the extent of their legal, technical and commercial responsibility.
3. 2. A power of attorney letter from the factory stating that the agency has been granted to the authorized agent in the United Arab Emirates
4. 3.A valid certificate of registration of the company in the country of origin, including the date of establishment,
5. stating clearly that the veterinary preparations produced by the company are authorized to be sold freely in the country of origin.
6. 4. A valid certificate issued by the concerned authorities in the country of the manufacturer proving its commitment to the principles of good practice in pharmaceutical manufacturing (GMP),
7. including evidence that the competent authorities have conducted periodic inspections on it.
8. 5. In case that the manufacturer site from an origin country that is not included in the list of countries mentioned in the terms and conditions,
9. a certificate of registration for the manufacturer site in at least two of these countries must be submitted.
10. 6. A list of the preparations produced by the factory. 7. Provide a Site Master File.

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