LIST
of foreign organizations, the results of which in terms of registration of medical equipment, medical devices and their supplements are recognized from June 1, 2021 in the Republic of Uzbekistan


Names
Country
1
Food and Drug Administration (FDA)
USA
2
Notified European bodies to issue the European Certificate of Conformity (CE)
European Union
3
European Medicines Agency (EMA)
European Union
4
Pharmaceuticals and Medical Devices Agency (PMDA)
Japan
5
Ministry of Food and Drug Safety (MFDS)
Republic of Korea
6
Medicines and Healthcare Products Regulatory Agency (MHRA)
Great Britain

Note:
Certificates must be issued for a medical product. The term of registration by the recognition method is 1 month, after payment of the state fee.



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See also:

Registration of medicines in Uzbekistan
Registration of medical device and medical equipment in Uzbekistan
Registration of dietary supplement and biologically active additives (BAA) in Uzbekistan
Registration of food additives and food supplements in Uzbekistan
Registration of cosmetics and perfumes, chemical substances, biological agents and materials, polymer and plastic materials in Uzbekistan
Registration of veterinary medicinal products, medicines, drugs and feed additives in Uzbekistan




Pharmacopoeia Committee

Tasks of the Pharmacopoeia Committee:

- examination of normative documents for medicines subject to registration and extension of the term of registration;
- systematic revision of normative documents for medicines with a view to improving their quality and improving the methods of control;
- examination and preparation for approval of...


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Department of Registration

Tasks of the Registration Department:

- after the adoption of the application for registration, conducts the initial (preliminary) examination of the application and attached registration documents and samples of medicines, medical devices and medical equipment;
- conducts appropriate correspondence with...;

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Pharmacological Committee

Tasks of the Pharmacological Committee:

- conducts examination of administrative, pharmacological, toxicological and clinical parts of registration documents of pharmacological and (or) medicinal products;
- conducts examines and re-examines documents of pharmacological and (or) medicinal products with the involvement of...;


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