There are various forms of representation (operating models) of foreign pharmaceutical companies in the Belarusian pharmaceutical market. In particular:
Let’s briefly look at the advantages and disadvantages of the main working models.
Objectives: preparatory and support activities, including advertising, promotion of medicines, market research.
A representative office of a foreign pharmaceutical company may be established only for the purpose of carrying out activities of a preparatory and support nature in relation to the parent organisation, such as the promotion of goods or registration actions in relation to medicines.
Such representative office is not allowed to conduct commercial activities, including agreeing the essential terms of dealings, signing commercial contracts, making decisions when participating in public procurement, etc.
If the above restrictions are violated, the consequences may be:
Objectives: independent import and sale of medicines in Belarus and the EAEU, localisation of production, participation in public procurement.
Allows to increase the margins of the supply chain in the group of companies, distribute financial flows across regions, etc.
The EAEU market is over 180 million people which motivates many pharmaceutical companies to set up local production facilities.
Localisation of production may provide customs, tax, administrative and other advantages.
For example, when participating in public procurement, domestic producers are entitled to a preferential adjustment of 15 per cent for goods originating in Belarus.
Foreign companies can participate in public procurement procedures, but, as a rule, it is difficult in practice due to language barriers, lack of necessary infrastructure, and short timeframes for submitting bids.
Such a legal entity can be responsible for the certain “region” in the group of companies: participate in public procurement with understanding of the parent companies’ pricing procedure, import medicines to the EAEU market, export goods within the EAEU and not only, advertise and promote products.
Objectives: minimal presence in the jurisdiction, minimising risks and/or transferring them to a third-party distributor.
In this model of operation, by transferring the goods to the carrier, the pharmaceutical company removes a number of different potential risks (licensing, incorrect pricing, storage, promotion, sales, etc.).
A sub-species of this model of operation is operating through pharmaceutical companies, which represent separate business units of transnational biopharmaceutical corporations.
In distribution agreements, pharmaceutical companies reward sales growth, advertising and marketing activities with various incentive payments. In other words, the distributor fulfils the function of both distributor and advertiser in relation to the products.
If the foreign pharmaceutical company itself wants to set the “advertising” policy, this model of work is supplemented by the establishment of a “non-commercial” representative office of the foreign organisation for the purposes of product promotion.
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