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Food Supplement Registration in Uzbekistan

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Food Supplement Registration in Uzbekistan

Regulatory Authority

Pharmaceutical Industry Development Agency

Regulatory Website

https://www.dra.gov.pk/

Registration Timeline

6-10 Months

License Validity

5 Years

Documents for Food Supplement Registration in Uzbekistan

  • The applicant’s legalized Power of Attorney to the representative
  • A legalized extract from the applicant’s registered legal entity.
  • Legalized copies of the manufacturer’s authorizations for each manufacturing site involved in the manufacturing process, issued by the relevant authorities of the manufacturer’s home country.
  • Authorized copies of the GMP Certificates for each manufacturing site used in the manufacturing process, issued by the relevant authorities of the applicant’s or manufacturer’s nation (if available).
  • Authorized copies of the registration certificate, issued by the relevant authorities of the applicant’s or manufacturer’s nation (if available); suggested mockups for the Uzbek market.
  • Certified copy of usage instructions or a summary of the product’s qualities (composition, form, description, shelf life, storage conditions, etc.).
  • A document attesting to the safety of prion-containing food supplements.
  • A description in Latin of the different types of living organism strains
  • A passport or strain certificate; or a description of the strains in food supplements.
  • The Latin names for plant parts, pharmacopoeial articles, shape and technique of preparation (for herbal food supplements), and a document attesting to the transmissive safety of food supplements containing blood components;
  • Scientific information
  • Food supplement control technique;

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