Disinfectants are a category where it’s not only about “what’s inside,” but also how everything is documented: composition, quality control methods, instructions for use, labeling, and safety. An incorrect wording or an incomplete document package often leads to returns, delays, and missed deadlines.
VITA CONSULT handles the entire process: we review the formulation and intended use, prepare the required documentation, coordinate testing (if needed), and support the expert review through to the final result. You get a clear plan, timeline control, and continuous communication—without endless revisions.
What’s included
consultation and selection of the optimal registration pathway
review of composition/intended use and product requirements
preparation of the document package: IFU/instructions, label, specifications, control methods, etc.
support with testing and obtaining reports (if required)
support throughout expert review and responses to comments
updates/changes to documents and dossier
timeline control and status reports
CTA
Send the composition and intended use—we’ll tell you which steps are required and where to start.
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.