Registration of veterinary products manufacturing site

Service Description

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

Service Process

• Log in using UAE PASS to start the service.
• Fill out the application form.
• Attach the required documents.
• Pay the fees.

Conditions & Requirements

• The applicant must be submitting by a licensed warehouse with valid license
• The list of countries permitted to register manufacturer site, including 1. ARGENTINA 2. AUSTRALIA 3. AUSTRIA 4. BELGIUM 5. BRAZIL 6. CANADA 7. 5CYPRUS 8. CHILE 9. CHINA 10. COLOMBIA 11. COSTA RICA 12. CZECH REPUBLIC 13. DENMARK 14. ESTONIA 15. FINLAND 16. FRANCE 17. GERMANY 18. GREECE 19. HUNGARY 20. ICELAND 21. IRELAND 22. ITALY 23. JAPAN 24. KOREA 25. LATVIA 26. LITHUANIA 27. LUXEMBOURG 28. MALTA 29. MEXICO 30. NETHERLANDS 31. NEW ZEALAND 32. NORWAY 33. POLAND 34. PORTUGAL 35. ROMANIA 36. RUSSIA 37. SAUDI ARABIA 38. SLOVAK REPUBLIC 39. SLOVENIA 40. SOUTH AFRICA 41. SPAIN 42. SWEDEN 43. SWITZERLAND 44. TURKEY 45. UNITED KINGDOM 46. UNITED STATES

Required Documents

• 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.
• The company's relationship with each of these factories and the extent of their legal, technical and commercial responsibility.
• 3. A valid certificate of registration of the company in the country of origin, including the date of establishment, stating clearly that the veterinary preparations produced by the company are authorized to be sold freely in the country of origin.
• 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), including evidence that the competent authorities have conducted periodic inspections on it.
• 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, a certificate of registration for the manufacturer site in at least two of these countries must be submitted.
• 6. A list of the preparations produced by the factory.