Registration of veterinary products manufacturing company

Service Code D2-2-AAA-17-APH
Number of Users

59 Companies

0 Individuals
Number of Transaction

185 Companies

0 Individuals
Target Audience

Companies
Service Channels

Start Service

Tutorial Video Download Form

File Name: D2-2-AAA-17-APH - V3 _2021.pdf

File Size: 145KB

File Type: PDF

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Service Time

The Estimated time to submit a service request : 10 minutes / The time to obtain the service: 20 working days

Customer Happiness Centers

Call Center

8003050

Email

info@moccae.gov.ae

User manual

Web Mobile

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

To apply for a service over any of the service channels, you should register in the digital services system From here

Fill out the electronic form
E- Payment
Study and review the documents electronically
Issuing a registration certificate electronically

Service Fees

5000 AED \ 5 years Request for issuance or renewal of registration certificate for manufacturer of veterinary products

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 power of attorney letter from the factory stating that the agency has been granted to the authorized agent in the United Arab Emirates
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.
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.
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.
A list of the preparations produced by the factory.
Provide a Site Master File.