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PHARM GROUP assists to foreign and domestic companies in the issues of government legalization of their products (drugs, APIs, medical equipments) in Uzbekistan:
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State registration (re-registration) of drugs, APIs medical supplies and equipments;
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Medical translations (to/from: English, Russian, Uzbek languages);
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Promoting the interests of foreign pharmaceutical companies;
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Marketing researches;
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Selection of distributors, dealers and whole sellers for the companies;
1. Assistance in registration (re-registration) of drugs and medical supplies:
The experts from PHARM GROUP will implement the procedures of turnkey drugs registration (translation of the paragraphs required and preparing the documents set, rendering of all consulting services required, development of AND, TND (nomenclatorial code of goods), guidelines and package labelling, copying the portfolio, submitting the portfolio and the Application, accompanying the portfolio during the expertise, obtaining the admittance, custom clearance of the samples, constant informing on the process of work executed, delivery of the certificate of registration). We can also carry out the specific work – medical translations, preparing the AND, TND (nomenclatorial code of goods), guidelines, labeling the package.
The terms of certifying the drugs in Uzbekistan with the help of our company:
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Translation and preparing the portfolio, development of AND, TND (nomenclatorial code of goods), guidelines, and package model on the background of the Client’s docs – 1 to 2 months.
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Submitting the Application and registration portfolio for the medicine to the Main Administration of Drugs and Medical Equipment Quality Control under the Ministry of Health of the Republic of Uzbekistan, presenting the Client’s interests during the expertise for the documentation, admittance and custom clearance of the medicine samples and reference standards, implementation of the quality inspection approaches at the lab, approval of the medical product at the meeting of the Main Administration of Drugs and Medical Equipment Quality Control under the Ministry of Health of the Republic of Uzbekistan, and obtaining the license – from 3 months for generic medicine and from 4 months for the authentic drug.
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Assistance when changing the package design, labeling, etc.
Certification of drugs in Uzbekistan is regulated by a great number of legal acts, resolutions, decrees, guidelines and orders.
2. Door to door promotion of the manufacturer:
- Sending printed materials to all 50 local large importers/whole sellers/distributors/producers.
- Arranging a meeting and making presentation of the company and drugs to the all local companies one by one.
- In case of interest of local partners, helping them to communicate with company representative to discuss different issues.
The price of such services costs $50 per company.
Deliverable: meeting reports with signature and contacts of company representative.
3. Marketing services:
- Research on promotion;
- Branding the drugs;
- Strategic Development;
4. The work of managers and medical representatives:
- Work with the Educational Institutions
- Holding the conferences (inviting of foreign lecturers is possible)
- Holding the Round Table Talks
- Holding the presentations at medical establishments
- Individual work with physicians
- Work with opinion leaders
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