Food Supplement Registration in Uzbekistan

Regulatory Authority Pharmaceutical Industry Development Agency Regulatory Website

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

5 Years

• 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;