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WTO notification · TBT

UkraineProposed measure, not in force yet

Human blood; animal blood for therapeutic – Ukraine

Official title

Draft Resolution of the Cabinet of Ministers of Ukraine 'Certain Issues Related to the Importation and Quality Control of Medicines'

Ukraine notified a revised version of this proposed TBT measure on 8 September 2026. The measure was first notified on 4 June 2026. The comment period closed on 8 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:

Updated here:

At a glance

Products

Medicines

HS codes
  • 30 · Pharmaceutical products
    • 3002 Human blood; animal blood prepared for therapeutic, prophylactic or diagnostic uses; antisera and other blood fractions and immunological products, whether or…
Notifying member
Ukraine
Status
Proposed measure, not in force yet
Objectives
  • Quality requirements
  • Harmonization
  • Reducing trade barriers and facilitating trade
Area
TBT: Technical product rulesTechnical barriers to trade
Notification type
Regular notification
Document symbol
G/TBT/N/UKR/384Latest notice: G/TBT/N/UKR/384/Rev.1

Key dates

Distributed by the WTO
Comment deadline
Closed on 8 October 2026
Proposed adoption
To be determined
Proposed entry into force
To be determined

How to comment

The comment period closed on 8 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/384/Rev.1; 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 Resolution has been developed with the aim of regulating the procedures for the importation of medicinal products (excluding active pharmaceutical ingredients) into Ukraine, conducting state quality control of imported medicinal products in a state laboratory or a laboratory authorized by the Ukrainian Pharmaceutical Agency, and carrying out the official batch release of certain biological medicinal products (immunological medicinal products and medicinal products derived from human blood or blood plasma). The draft Resolution is aimed at implementing the Law of Ukraine No. 2469-IX of 28 July 2022 'On Medicines' and establishing a unified regulatory framework for the relevant procedures applicable to medicinal products imported into Ukraine. Specifically, the draft Resolution provides for: Approval of new procedures and criteria: Procedure for conducting state quality control of medicinal products in a state laboratory or a laboratory authorized by the Ukrainian Pharmaceutical Agency; Procedure for the official batch release of certain biological medicinal products (immunological medicinal products and medicinal products derived from human blood or blood plasma); Criteria for establishing an annual programme (plan) for the sampling of medicinal products and the grounds for conducting ad hoc laboratory quality control of medicinal products. Transitional and special provisions for importers: Establishing a one-year transitional period starting on 1 January 2027…

Notices on this measure

Every notice about this measure published here, newest first. Each one is the notifying member's own text.

  1. RevisionG/TBT/N/UKR/384/Rev.1

    Comment deadline: Closed on 8 October 2026

    Draft Resolution of the Cabinet of Ministers of Ukraine 'Certain Issues Related to the Importation and Quality Control of Medicines'

    The draft Resolution has been developed with the aim of regulating the procedures for the importation of medicinal products (excluding active pharmaceutical ingredients) into Ukraine, conducting state quality control of imported medicinal products in a state laboratory or a laboratory authorized by the Ukrainian Pharmaceutical Agency, and carrying out the official batch release of certain biological medicinal products (immunological medicinal products and medicinal products derived from human blood or blood plasma). The draft Resolution is aimed at implementing the Law of Ukraine No. 2469-IX of 28 July 2022 'On Medicines' and establishing a unified regulatory framework for the relevant procedures applicable to medicinal products imported into Ukraine. Specifically, the draft Resolution provides for: Approval of new procedures and criteria: Procedure for conducting state quality control of medicinal products in a state laboratory or a laboratory authorized by the Ukrainian Pharmaceutical Agency; Procedure for the official batch release of certain biological medicinal products (immunological medicinal products and medicinal products derived from human blood or blood plasma); Criteria for establishing an annual programme (plan) for the sampling of medicinal products and the grounds for conducting ad hoc laboratory quality control of medicinal products. Transitional and special provisions for importers: Establishing a one-year transitional period starting on 1 January 2027…

  2. Regular notificationG/TBT/N/UKR/384

    Comment deadline: Closed on 4 July 2026

    Draft Resolution of the Cabinet of Ministers of Ukraine 'Certain Issues Related to the Importation and Quality Control of Medicines'

    The draft Resolution has been developed to regulate the procedures for imports of medicines (except active pharmaceutical ingredients) into the territory of Ukraine, the state quality control of medicines imported into Ukraine, quality control testing of medicines in a state laboratory or a laboratory authorised by a state control authority and the official batch release of certain biological medicines (immunological medicinal products and medicinal products derived from human blood or plasma). The draft Resolution proposes to amend the Resolution of the Cabinet of Ministers of Ukraine No. 287 of 14 March 2025 'On Approval of the Procedure for Importation of Medicines into the Territory of Ukraine' in order to establish a unified procedure for the importation of medicines and the state quality control of medicines imported into the territory of Ukraine. The draft Resolution also provides for the approval of the Procedure for State Quality Control of Medicines Conducted in a State Laboratory or a Laboratory Authorized by the State Control Authority; the Procedure for Official Batch Release of Certain Biological Medicines (Immunological Medicinal Products and Medicinal Products Derived from Human Blood or Human Plasma); the Criteria for Establishing the Annual Programme (Plan) for Sampling of Medicines and repeal certain resolutions of the Cabinet of Ministers of Ukraine, including Resolution No. 902 of 14 September 2005 'On Approval of the Procedure for State Quality Control…

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