Registration of food additives and food supplements in Uzbekistan
List of documents submitted for state registration of food additives in the Republic of Uzbekistan



1
Application of established form.
2
Specification (characteristic) of a food additive with an indication of the composition, purpose and dose of use.
3
Samples of food additives in the amount necessary for toxico-hygienic assessment.
4
For imported food additives, a safety certificate or registration certificate of manufacturing country (if any) is additionally presented.
5
For food additives produced in the Republic of Uzbekistan, additional normative documents is provided (organization standards, processing instructions and formulation).

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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 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 additions and amendments of the...

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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 the applicant on the...

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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 independent experts;
- decides on the use of the medicines without clinical trials in the...

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