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WTO notification · TBT

UkraineProposed measure, open for comments

Laboratory medicine – Ukraine

Official title

Draft Order of the Ministry of Health of Ukraine 'Certain Issues of Maintaining the State Register of Clinical Studies (Trials) of Medicinal Products'

Ukraine notified this proposed TBT measure to the WTO on 15 October 2026. Comments are open until 14 November 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

Medicinal products

Notifying member
Ukraine
Status
Proposed measure, open for comments
Objectives
  • Harmonization
  • Other
Area
TBT: Technical product rulesTechnical barriers to trade
Notification type
Regular notification
Document symbol
G/TBT/N/UKR/419
ICS classification
  • 11.100 Laboratory medicine
Keywords
Human health

Key dates

Distributed by the WTO
Comment deadline
Open until 14 November 2026
Proposed adoption
To be determined
Proposed entry into force

How to comment

Comments on a notification go from government to government. If this measure affects your exports, send your comments to your country's WTO TBT enquiry point before 14 November 2026, quoting the document symbol G/TBT/N/UKR/419 and how the measure affects your products. Your enquiry point forwards them to Ukraine.

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

What the notification says

The draft Order provides for the approval of: the Procedure for Maintaining the State Register of Clinical Studies (Trials) of Medicinal Products; amendments to the Procedure for Conducting Clinical Studies (Trials) of Medicinal Products, approved by Order of the Ministry of Health of Ukraine No. 184 of 16 February 2026. The draft Order establishes the regulatory framework for maintaining and operating the electronic State Register of Clinical Studies (Trials) of Medicinal Products in Ukraine, specifies the information to be published therein, establishes procedures for the initial entry and updating of information on clinical trials, and ensures public access to such information.

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