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Registration of medicinal products in Uzbekistan

List of countries and international organizations whose drug registration results are recognized in the Republic of Uzbekistan

Countries List of regulatory authorities included in the World Health Organization (WHO) Listed Authorities and/or those with Maturity Level 4 (ML-4) status
1 Austria Austrian Federal Office for Safety in Health Care (BASG — Bundesamt für Sicherheit im Gesundheitswesen).
2 Belgium Federal Agency for Medicines and Health Products (FAMHP).
3 Bulgaria Bulgarian Drug Agency (BDA).
4 Canada Health Canada.
5 Croatia Agency for Medicinal Products and Medical Devices of Croatia (HALMED – Agencija za lijekove i medicinske proizvode).
6 Cyprus Pharmaceutical Services, Ministry of Health (PHS-MoH).
7 Czech Republic State Institute for Drug Control (SUKL – Státní ústav pro kontrolu léčiv).
8 Denmark Danish Medicines Agency (DKMA – Danish Lægemiddelstyrelsen Medicines Agency).
9 Estonia State Agency of Medicines (SAM).
10 European Medicines Regulatory Network
11 Finland Finnish Medicines Agency (FIMEA).
12 France French National Agency for Medicines and Health Products Safety (ANSM — Agence nationale de sécurité du médicament et des produits de santé).
13 Germany Federal Institute for Drugs and Medical Devices (BfArM – Bundesinstitut für Arzneimittel und Medizinprodukte).
14 Greece National Organization for Medicines (EOF – Εθνικός Οργανισμός Φαρμάκων).
15 Hungary National Center for Public Health and Pharmacy (NNGYK – Nemzeti Népegészségügyi és Gyógyszerészeti Központ).
16 Iceland Icelandic Medicines Agency (IMA).
17 Ireland Health Products Regulatory Authority (HPRA).
18 Italy Italian Medicines Agency (AIFA — Agenzia Italiana del Farmaco).
19 Japan Ministry of Health, Labour and Welfare (MHLW) / Pharmaceuticals and Medical Devices Agency (PMDA).
20 Latvia State Agency of Medicines of Latvia (ZVA — Zāļu Valsts Aģentūra).
21 Liechtenstein Office of Health / Medicinal Products Control Agency (LLV — Liechtensteinische Landesverwaltung).
22 Lithuania State Medicines Control Agency (VVKT — Valstybinė vaistų kontrolės tarnyba).
23 Luxembourg Ministry of Health and Social Security of Luxembourg.
24 Malta Malta Medicines Authority (MMA).
25 Netherlands Medicines Evaluation Board (CBG-MEB — College ter Beoordeling van Geneesmiddelen — Medicines Evaluation Board).
26 Norway Norwegian Medical Products Agency (NOMA).
27 Poland Office for Registration of Medicinal Products, Medical Devices and Biocidal Products (URPL — Urząd Rejestracji Produktów Leczniczych).
28 Portugal National Authority of Medicines and Health Products, I.P. (INFARMED — Autoridade Nacional do Medicamento e Produtos de Saúde).
29 Republic of Korea (South Korea) Ministry of Food and Drug Safety (MFDS).
30 Romania National Agency for Medicines and Medical Devices of Romania (NAMMDR).
31 Saudi Arabia Saudi Food and Drug Authority (SFDA).
32 Singapore Health Sciences Authority (HSA).
33 Slovakia State Institute for Drug Control (SUKL — Státní ústav pro kontrolu léčiv).
34 Slovenia Agency for Medicinal Products and Medical Devices of the Republic of Slovenia (JAZMP — Javna agencija Republike Slovenije za zdravila in medicinske pripomočke).
35 Spain Spanish Agency of Medicines and Medical Devices (AEMPS — Agencia Española de Medicamentos y Productos Sanitarios).
36 Sweden Swedish Medical Products Agency (SMPA).
37 Switzerland Swiss Federal Agency (Swissmedic).
38 United Kingdom Medicines and Healthcare products Regulatory Agency (MHRA).
39 United States of America (USA) US Food and Drug Administration (US FDA).

Note:

  • The registration period using the recognition method is on average 1-2 months after payment of the state fee.

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See also:

Documents required for state registration of medicines in the Republic of Uzbekistan
Documents required for state registration of medical devices and medical equipment in the Republic of Uzbekistan
Documents required for state registration of dietary supplements in the Republic of Uzbekistan
Documents required for state registration of food additives in the Republic of Uzbekistan
Documents required for state registration of cosmetics, chemicals, biological agents and materials, polymers and plastics in the Republic of Uzbekistan
Documents required for state registration of veterinary products in the Republic of Uzbekistan

See also other products:

Medicines
Medical devices and Medical Equipment
Dietary Supplements
Food Additives
Cosmetics, Chemicals, Biological Agents and Materials, Polymers and Plastics
Veterinary Medicines

See also other state duties:

State duty for registration of medicines in the Republic of Uzbekistan
State duty for registration of medical devices and medical equipment in the Republic of Uzbekistan
State duty for registration of dietary supplements in the Republic of Uzbekistan
State duty for registration of food additives in the Republic of Uzbekistan
State duty for registration of cosmetics, chemicals, biological agents and materials, polymers and plastics in the Republic of Uzbekistan
State duty for registration of veterinary medicines and feed additives in the Republic of Uzbekistan

See also:

List of foreign organizations whose results in terms of registration of medical equipment, medical devices and their components are recognized in the Republic of Uzbekistan from June 1, 2021

See also departments:

Registration Department
Pharmacological Committee
Pharmacopoeial Committee
Committee on New Medical Technology (CNMT)
Laboratory for quality control and standardization of medicines
Laboratory of vaccines, serous drugs and microbiological research/a>
Laboratory for quality control of medical devices and medical equipment
Laboratory of Pharmacotoxicological Research
Department of Pharmacovigilance (PV Dept)
Department for the implementation of special digital markings
Quality Management Systems Certification Body
Reference Pricing Department