Specialized food products (infant nutrition, dietary, therapeutic/preventive, and products for special needs) require strict compliance with composition, labeling, and documentation requirements. In practice, the process is often delayed by “small details”: incorrect wording, an incomplete document package, or inconsistencies in the label or test reports.
VITA CONSULT takes care of the full support: we review the composition and claimed properties, prepare the dossier, assist with testing, and take the process through to obtaining the required permits/authorizations. You get a clear plan, timeline control, and continuous communication—without stress and endless revisions.
What’s included
consultation and selection of the optimal registration pathway
preliminary review of composition and requirements
preparation and оформление of the document package and dossier
review of labeling and texts (to avoid rejection during review)
arranging tests and obtaining reports (if required)
support throughout expert review, responses to comments, and corrections
timeline control and status reports
CTA
Send the composition and label—we’ll tell you what’s needed for registration and outline the next steps.
The main legislative acts regulating marketing authorization and circulation of medicines are the Law of Uzbekistan "On Medicines and Pharmaceutical Activities", Resolution dated March 23, 2018 No. 213
Additions to the State Register of medicines and medical devices and medical equipment approved for use in medical practice of the Republic of Uzbekistan No. 26, 2022 2-sq. (07/19/2022).
The List of countries and international organizations has been approved, the results of registration of medicines of which will be recognized from November 1, 2018.