Supplying the pharmaceutical needs of the country’s veterinary network
- Registering products in the shortest time
- Choosing the best type of product by measuring the needs of country’s pharmaceutical market
- Determining the amount of product import by knowing the market potential and the presence of similar products in the market
- Selling Products by having the most professional sales team in reputable companies
Examining market needs and smart imports based on reverse engineering is the most important policy of NOJAN MEHR Company
Drug Registration
The result of a process is the product of realistic planning and regular follow-up of activities.
In the process of drug registration, the applicant for drug registration (the experts of Nojan Mehr Company) and the IVO experts must complete the required activities at the right time so that the next steps can be done well and without problems.
One of the important needs of realistic planning is having appropriate and correct information. First of all, we make sure to inform our employers so that the necessary information for realistic planning is always available.
Registering in IVO is the first step of importing a product. At first step, as the official representative of the foreign manufacturer, the Iranian company must deliver the following documents to the drug and treatment office of the IVO along with its application letter.
Certificate of analysis: COA
The list of countries in which the product has been exported
Drug Master file or Vaccine Master file : Master File
- Having international approvals (FDA approval) or sales history in EU is necessary for registering drugs and vaccines in Iran.
- The process of registering each product takes from 6 months to a year.
- European and American pharmaceutical companies that are approved by the FDA have a special place among Iranian consumers due to their product quality and high effectiveness. This has caused companies with no FDA approves to break their prices to be able to enter the Iranian market.
- These strict rules are only for the registration of drugs and vaccines in Iran, and the import of pet products, vitamins or pharmaceutical raw materials have easier rules.
After submitting the documents to the Iranian Veterinary Organization (IVO) and obtaining preliminary approvals, the Iranian company which has introduced itself as an exclusive representative of a foreign manufacturing company, must import a sample of the product to be tested in the laboratory of the Veterinary Organization’s Diagnostic Center.
After obtaining the laboratory approvals, the experts of the IVO will visit the manufacturer’s factory if needed.
After obtaining the Registration Certificate and IVC code, company can import the product.
Drug Importation
The product import process begins with registering information in the comprehensive trade system and creating a file, and the result of the action, after going through the systematic steps of this request, is automatically displayed on the user panel of the representative company on the pharmaceutical website of the Veterinary Organization.
By registering the import application along with the proforma and the analysis sheet, the representative company continues the application registration process in the drug and treatment office of the veterinary organization. This request is reviewed by the experts of the veterinary organization.
If approved, the entry permit will be issued by the veterinary organization. Due to the connection between the two comprehensive trade systems and the veterinary organization, the obtained licenses are placed on the trade system and the rest of the steps can be followed in this system. After obtaining the necessary permits from the Comprehensive Trade System of the Ministry of Mining Industry and Trade and Jihad Agriculture, it is possible to import the product.
At the same time as obtaining the permits of the Veterinary Organization and the Ministry of Agricultural Jihad, the necessary proceeds will be taken to buy foreign currency and transfer money, which is the responsibility of the banks of the commercial parties to transfer money and exchange documents.
After the cargo arrives in the country, the representative company obtains a clearance permit, after the cargo is transported from the customs to the warehouse of the national distribution company, a distribution license is obtained, and it is at this time that the national distribution company will be allowed to sell the product.
Step one
Step two
In the following
Selling Medicine
After transporting the drug to the warehouses of a national distribution company and obtaining the necessary license, this company is able to sell the product to provincial distribution companies. At this stage, provincial distribution companies will be able to sell the product to pharmacies. Finally, pharmacies provide the product to the final consumer.
Nojan Mehr Company distributes imported medicines to the consumer network through cooperation with prominent nationwide distribution companies, such as Pars Hel Daru Company and Parsian Pakhsh Exir Distribution Company.
NOJAN MEHR
Email: info@nojanmehr.co
Tell: 26200855 – 8
Fax: 22035409
Address: Apt.11, 3rd Flr., No.32, Golfam Ave., Africa Bvld.
Tehran-IRAN
Fa