Committee on New Medical Technology (CNMT)

Committee on New Medical Technology (CNMT) is a structural subdivision of the State Institution "Center for Pharmaceutical Product Safety" under the Ministry of Health, which organizes and coordinates work on quality control and registration of medical products of domestic and foreign manufacture: apparatus, instruments, equipments, medical devices and in vitro diagnostic tools.

Tasks of the Committee on New Medical Technology (CNMT)

  • Recommendation for State registration (re-registration) of medical devices and medical equipment in accordance with the Resolution of the Cabinet of Ministers of the Republic of Uzbekistan «On Approval of the Regulation on the Procedure for State Registration of Medicines and the Regulation on the Procedure for State Registration of Medical Devices» dated 02/26/2026 No.738 and recommendation for State registration of medical devices and medical equipment in accordance with the Decree of the President of the Republic of Uzbekistan «On the consistent continuation of reforms in the healthcare system and the creation of the necessary conditions to increase the potential of medical workers» dated 05/05/2021 No. 6221.
  • Organization and implementation of examination of laboratory, technical and clinical tests.
  • Coordination of normative documentation for medical devices.
  • Preparation of materials for the creation of the State Register of medical devices approved for use in healthcare practice in the Republic of Uzbekistan.
  • Consideration and submission for approval of standards for medical devices proposed for production.
  • Consideration of issues of international cooperation in the areas of the Committee’s activities.
  • Participation in the creation of the State Pharmacopoeia of the Republic of Uzbekistan.
  • Consideration of applications and proposals for the registration of medical devices, management of documentation related to these matters.
  • Conducting an examination of the compliance of normative documentation and samples of medical devices with the requirements of state, interstate and international standards.
  • Coordination and submission for approval, in accordance with the established procedure, of draft standards, TPM, MPM, PM, technical specifications, instructions for use, and production regulations.
  • Consideration of the results of laboratory studies and technical tests and making decisions on the registration and use of medical devices in healthcare practice, or making decisions on conducting clinical trials, if necessary.
  • Organization of clinical trials.
  • Consideration of clinical trial results and decision-making on recommendations for registration and use of medical devices in healthcare practice.
  • Approval or re-approval of the nomenclature of medical devices, in accordance with established procedures, for the development of recommendations on their modernization or discontinuation of industrial production.
  • Participating in the development of departmental normative documents and draft orders of the Ministry of Health of the Republic of Uzbekistan regarding the authorization of new medical devices for medical use and the removal from the nomenclature of obsolete or medically unused devices.
  • Reviewing and preparing for approval guidance documents (GD), methodological guidelines, bulletins, and information sheets related to new medical devices.
  • Preparation of draft regulatory documents regulating the Committee’s activities.
  • Submitting proposals for the introduction of new regulatory documents and for the cancellation, restriction, or extension of validity of obsolete TPM, MPM, PM, TS for medical devices.
  • Systematic review of the nomenclature of medical devices approved for medical use, to ensure timely inclusion of new devices in the State Register and removal of obsolete devices.
  • Engaging, when necessary, specialists from various enterprises, organizations, and institutions, in coordination with their management, as well as technical resources for conducting expertise and quality control of medical devices, including subcontracted laboratories.

See also other products:


See also:


See also other state duties:


See also:


See also departments:




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Pharmacological Committee Approval of instructions for...
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Committee on New Medical Technology (CNMT) Recommendation for State registration...
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