Tajikistan

The population of Tajikistan is 8.8 million people. Import plays a very important role, and its share is more than 90% of the country’s pharmaceutical market. Total health expenditure is about 7% of the state budget, growth is about 10% per year.

Import and sale of medicinal products are allowed only after state registration. To import medical devices and medical equipment, it is also necessary to obtain a Marketing Authorization. Food supplements and therapeutic agents, baby food, sanitary-hygienic products and cosmetics that have therapeutic and preventive properties in accordance with the law are included in the list of mandatory certification and also undergo state registration.

 

Competent authorities:

Ministry of Health and Social Protection of the Population of the Republic of Tajikistan
The central executive body that implements public health policy
Web site: https://moh.tj/  

State Supervision Service for Health Care and Social Protection of the Population of the Republic of Tajikistan
Expert evaluation of documentation for registration purposes, state supervision of pharmaceutical activities
Web site: http://www.pharmnadzor.tj/  

Agency for Standardization, Metrology, Certification and Trade Inspection under the Government of the Republic of Tajikistan
The authorized body for standardization, metrology, certification and trade inspection, sanitary and epidemiological surveillance of the Republic of Tajikistan.
Web site: http://www.standard.tj/ 

 

The main legislative acts:

  1. Law of the Republic of Tajikistan “On Protection of Public Health”;
  2. Law of the Republic of Tajikistan “On Medicines and Pharmaceutical Activity”;
  3. Decree of the Government of the Republic of Tajikistan “On the State Supervision Service for Pharmaceutical Activity”;
  4. Decree of the Government of the Republic of Tajikistan No. 210 dated May 3, 2010 “On Approval of the Procedure for Certification of Medicines and Medical Goods”;
  5. Ordinance of the Ministry of Health and Social Protection of the Population of the Republic of Tajikistan No. 736 dated August 21, 2015 “On Approval of the Procedure for State Registration of Medicines and Medical Goods in the Republic of Tajikistan”;
  6. Decree of the Government of the Republic of Tajikistan “On Rules for the Import and Export of Medicines and Medical Goods, and Narcotic Drugs, Psychotropic Substances and Precursors Used in Medicine in the Republic of Tajikistan”.

 

Cratia provides professional services of state registration of medical (healthcare) products in Tajikistan. We have an excellent knowledge of national legislation, necessary experience and resources. We offer:

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(name, formulation, dose and route(s) of administration, date of therapy start)