Pharmacological Committee

The Pharmacological Committee (PC) is a structural division of the State Institution «Center for Pharmaceutical Product Safety» under the Ministry of Health, responsible for the expert assessment of the efficacy and safety of medicinal products intended for use in medical practice.
Procedural matters of the PC are administered by its Presidium.
Specialized commissions of the PC:

  • Commission on Immunobiological Products.
  • Nomenclature Commission.

Tasks of the Pharmacological Committee

  • Evaluation of preclinical studies on the efficacy and safety of medicinal products.
  • Authorization of clinical trials for medicinal products, determination of the type and scope of clinical studies, and assessment of clinical trial reports.
  • Authorization of medicinal products for use in medical practice.
  • Approval of instructions for use for domestically manufactured medicinal products and review of instructions for use submitted by foreign manufacturers.
  • Monitoring of adverse drug reactions and development of specific measures for their prevention or mitigation (including recommendations for withdrawal from medical use).
  • Preparation and regular updating of the list of over-the-counter medicinal products.
  • Provision of methodological and advisory support to developers, manufacturers, and clinical sites in organizing their activities.

See also other products:


See also:


See also other state duties:


See also:


See also departments:




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