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WTO notification · TBT

KyrgyzstanProposed measure, may since have been adopted

Pharmaceutical products – Kyrgyzstan

Official title

Draft amendments to the Rules of Good Manufacturing Practice in the Eurasian Economic Union

Kyrgyzstan notified this proposed TBT measure to the WTO on 17 November 2025. The comment period closed on 14 December 2025.

Expodite puts notifications like this one in your Updates centre, matched to the HS codes of your products and the markets you export to. Opens the requirements check for Kyrgyzstan in your Expodite account.

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

Published here:

At a glance

Products

(Pharmaceuticals)

HS codes
  • 30 · Pharmaceutical products
    • 3003 Medicaments consisting of two or more constituents mixed together for therapeutic or prophylactic uses, not in measured doses or put up for retail sale (excl…
    • 3004 Medicaments consisting of mixed or unmixed products for therapeutic or prophylactic uses, put up in measured doses 'incl. those for transdermal…
Notifying member
Kyrgyzstan(Kyrgyz Republic)
Status
Proposed measure, may since have been adoptedNotified as a draft on 17 November 2025. Check WTO ePing or Kyrgyzstan for its current status.
Objectives
  • Protection of human health or safety
Area
TBT: Technical product rulesTechnical barriers to trade
Notification type
Regular notification
Document symbol
G/TBT/N/KGZ/61
Keywords
Human health

Key dates

Distributed by the WTO
Comment deadline
Closed on 14 December 2025
Proposed adoption
Not less than 180 calendar days from the date of official publication
Proposed entry into force
Not less than 180 calendar days from the date of official publication

How to comment

The comment period closed on 14 December 2025. You can still raise concerns about the measure with your country's WTO TBT enquiry point, quoting the document symbol G/TBT/N/KGZ/61; it can take them up with Kyrgyzstan.

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

What the notification says

Supplementation of the Rules of Good Manufacturing Practice with Requirements for the production of high-tech medicines harmonized with the current version of the Rules of Good Manufacturing Practice of the European Union and relevant international standards to ensure stable quality of the production process of the specified group of drugs in order to promptly identify deviations in the production process, as a result of which the finished product will be recognized as substandard.

All updates from Kyrgyzstan
  1. WTO notificationSPSProposed measure, open for comments

    Draft Decision of the Collegium of the Eurasian Economic Commission on Amendments to Decision of the Customs Union Commission of 28 May 2010 No. 299

    The draft Decision amends Decision of the Customs Union Commission No. 299 of 28 May 2010 'On the Application of Sanitary Measures in the Customs Union'. The draft Decision supplements the said Decision with a new paragraph 2-2, establishing that where amendments are introduced to the Common…

    No products listed by the notifying member

    Symbol: G/SPS/N/KGZ/47Comments until 22 December 2026

  2. WTO notificationTBTProposed measure, not in force yet

    Draft Decision of the Council of the Eurasian Economic Commission amending certain decisions of the Council of the Eurasian Economic Commission

    The draft decision provides for the following: transition period extension until 31 December 2036 in order to prolong the period of circulation of diagnostic, disinfectant, disinfestation and deacarisational preparations for veterinary use in the territory of the Eurasian Economic Union (EAEU) in…

    Symbol: G/TBT/N/KGZ/67Comment period closed

  3. WTO notificationTBTProposed measure, not in force yet

    Draft amendments to the Rules for registration and examination of safety, quality and effectiveness of medical devices

    The draft amendments to the Rules for registration and examination of safety, quality and effectiveness of medical devices provides for the possibility of suspending the validity of the marketing authorization in the event that there is no valid report on the results of inspection in the marketing…

    Symbol: G/TBT/N/KGZ/66Comment period closed

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