Registration of veterinary medicinal products, medicines, drugs and feed additives in Uzbekistan
List of registration documents and samples required for registration of veterinary medicinal products (VMPs) and feed additives in the Republic of Uzbekistan


1
The list of components included in the composition of veterinary medicines and feed additives, their quantity.
2
Quality requirements and control methods for veterinary medicinal products and feed additives, texts of relevant international or state pharmacopoeial monographs.
3
Instructions (manuals) for use of veterinary medicinal products and feed additives.
4
Quality certificates or certificates of conformity of the veterinary medicinal products and feed additives.
5
Data on the manufacture of veterinary medicinal products and feed additives (technological instruction or regulations, manufacturing flowchart).
6
Test results for the efficacy, safety and stability of veterinary medicinal products and feed additives.
7
Substantiated information on the effectiveness, immunogenicity, virulence of veterinary biologics and microorganism strains that used in their production (viruses, bacteria, fungi, etc.).
8
Samples of veterinary medicinal products and feed additives in volumes sufficient for their technical testing specified in the documentation, and their active substances, test systems, diagnostic kits.


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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




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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