Issue a Registration Certificate for a Veterinary Products Manufacturer

Service Code

D2-2-AAA-17-APH

Service Description

Through this service, the registration of foreign manufacturers of veterinary products is approved through a veterinary warehouse licensed by the Ministry in order to allow the registration, import and circulation of its products in the country.

Service Procedures
  1. Submit the application
  2. Pay the prescribed financial fee for the application
  3. Study and review the documents
  4. Pay the prescribed financial fee for the registration
  5. Issuing a registration certificate
Note: to start applying on the service, please register and signup to have your personal user name in the system
Target Audience
Companies
Required Documents
  • Provide a file that includes the following basic information:
    1. Type and activity of the company.
    2. Number of factories owned by the company and its addresses.
    3. The company's relationship with each of these factories and the extent of their legal, technical and commercial responsibility.
  • A duly authorized power of attorney from the factory stating that the Agency has been granted to the authorized agent in the United Arab Emirates.
  • Certificate of registration of the company in the country of origin in force. Date of establishment duly certified. It is clear that the veterinary products produced by the company are authorized to sell freely in the country of origin.
  • A valid certified certificate issued by the relevant authorities in the country of the establishment confirming its commitment to the good practice of GMP including proof of the periodic inspection by the competent authorities. Certificate from the competent authorities of the country of origin (duly certified) that the company follows the principles of good practice for the manufacture of veterinary preparations.
  • A certified list of the company with the names of the countries registered with it, accompanied by copies of registration certificates (manufacture side should be registration in 2 reference country : ( UNITED STATES, CANADA, AUSTRALIA, JAPAN, EUROPEAN MEDICINES (BELGIUM, DENMARK, GERMANY, SPAIN, FRANCE, IRELAND, ITALY, LITHUANIA, HUNGARY, NETHERLANDS, AUSTRIA, ROMANIA, FINLAND, SWEDEN, SWITZERLAND, NEW ZEALAND, CYPRUS, CZECH REPUBLIC, ESTONIA, FINLAND, GERMANY, GREECE, LATVIA, LUXEMBOURG, MALTA, POLAND, PORTUGAL, SLOVAKIA AND SLOVENIA) SAUDI ARABIA, SOUTH AFRICA, KOREA)
  • A list of the preparations produced by the factory.
  • Description of the company's research and development activities.
  • Provide a Site Master File.

Pre-registered companies:

https://www.youtube.com/embed/reOnzkBn6qE
Terms and Conditions
  1. The applicant must be submitting by a licensed warehouse with valid license.
Used Forms

Issue Certificate of Registration of Manufacture Side

Service Time

40 Working days