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WTO notification · TBT

UkraineProposed measure, not in force yet

Pharmaceutical products – Ukraine

Official title

Draft Order of the Ministry of Health of Ukraine 'On Approval of the Procedure for Quality Control of Medicines During Wholesale and Retail Trade'

Ukraine notified this proposed TBT measure to the WTO on 14 September 2026. The comment period closed on 14 October 2026.

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Source: WTO ePing (opens in a new tab). Summaries by Expodite, which is independent of the WTO.

Published here:

At a glance

Products

Medicines

Notifying member
Ukraine
Status
Proposed measure, not in force yet
Objectives
  • Quality requirements
  • Harmonization
Area
TBT: Technical product rulesTechnical barriers to trade
Notification type
Regular notification
Document symbol
G/TBT/N/UKR/404
ICS classification
  • 11.120 Pharmaceutics

Key dates

Distributed by the WTO
Comment deadline
Closed on 14 October 2026
Proposed adoption
To be determined
Proposed entry into force

How to comment

The comment period closed on 14 October 2026. You can still raise concerns about the measure with your country's WTO TBT enquiry point, quoting the document symbol G/TBT/N/UKR/404; it can take them up with Ukraine.

Find your country's enquiry point on WTO ePing (opens in a new tab)

What the notification says

The draft Order proposes to approve a new Procedure for quality control of medicines during wholesale and retail trade, which establishes the mechanism for conducting incoming quality control of medicines by business entities licensed to conduct wholesale and retail trade in medicinal products, as well as for state supervision (control) in the field of medicines during their wholesale and retail trade. The draft has been developed with the aim of bringing the procedures for quality control of medicines into compliance with Law of Ukraine No. 2469-IX of 28 July 2022 'On Medicines', updating the relevant terminology, and establishing requirements for ensuring the quality of medicines during their wholesale and retail trade. The draft Order, in particular: establishes a 5-year retention period for documents confirming the procurement, storage, transportation, trade, destruction or disposal of medicines; proposes to include medicinal products not accompanied by a package leaflet in the list of medicines prohibited from sale; establishes incoming quality control of medicines at receiving areas through visual inspection by authorized persons before a decision is made to release the respective batches for sale; establishes the procedure for sampling medicines where doubts arise as to their quality or where falsification is suspected, and for submitting such samples to the territorial bodies of Ukrpharmagency for state laboratory quality control in accordance with Article 108 of…

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