EECEurasian Economic CommissionActivitiesTechnical regulationTechnical Regulation and Accreditation DepartmentSetting up of Common Market of Pharmaceutical ProductsMD_acts Chairman of the board of the EEC Organizational Support and Protocol DepartmentFinance DepartmentLegal DepartmentAdministrative Department Integration and Macroeconomics Integration Development DepartmentMacroeconomic Policy DepartmentStatistics Department Economy and financial policy Business Development DepartmentFinancial Policy DepartmentLabour Migration Department Industry and agriculture Industrial Policy DepartmentAgricultural Policy Department Trade Tariff and Non-tariff Customs Regulation DepartmentDepartment for Internal Market DefenceTrade Policy Departmentvideo_forum Technical regulation Technical Regulation and Accreditation DepartmentCurrently selectedSanitary, Phytosanitary and Veterinary Measures Department Customs cooperation Customs Infrastructure DepartmentDepartment of customs legislation and law enforcement practice Energy and infrastructure Energy DepartmentTransport and Infrastructure Department Competition and Antitrust regulation Department for antitrust regulationDepartment for Competition and Public Procurement Policy Internal markets, informatization, information and communication technologies Domestic Markets Operation DepartmentIT Department MD_acts EECEurasian Economic CommissionActivitiesTechnical regulationTechnical Regulation and Accreditation DepartmentSetting up of Common Market of Pharmaceutical ProductsMD_acts Last modified at 10/25/2018 9:25 AM by Шакирова Диана Ильдаровна Page ContentActs in the sphere of circulation of medical products Agreement on common principles and rules for the circulation of medical devices (medical products and medical equipment) in the framework of the Eurasian Economic Union On Regulation on the Advisory Committee for Medical Products On Criteria for differentiation of elements of a medical product that are components of the medical product for the purpose of its registration On Criteria for inclusion of several modifications of the medical product relating to one type of the medical product in accordance with the medical product nomenclature applied in the Eurasian Economic Union in one registration certificate On Approval of General Requirements for safety and efficacy of medical products, requirements for their marking and operational documentation on them On the list of standards, the application of which, on a voluntary basis, fully or partially ensures compliance of medical products with General Requirements for Safety and Efficacy of Medical Products, Requirements for Their Marking and Operational Documentation on Them On Approval of the List of Types of Medical Products subject to Assignment to Measuring Instruments during Their Registration On Requirements to the implementation, Maintenance and Evaluation of Medical Product Management System Depending on the Potential Risk of Their Use On Procedure for formation of the list of standards the application of which, on a voluntary basis, fully or partially ensures compliance of medical products with the General Requirements for Safety and Efficacy of Medical Products, Requirements for Their Marking and Operational Documentation on Them On the Requirements to the Electronic Form of Applications and Documents of the Registration Dossier Submitted when Registering and Examining Safety, Quality and Efficacy of Medical Products On Approval of Rules for Classification of Medical Products Depending on the Potential Risk of Their Use On Rules for Clinical and Clinical Laboratory Trials (Studies) of Medical Products On Rules for Keeping Medical Product Nomenclature On Rules for Registration and Examination of Safety, Quality and Efficacy of Medical Products On Approval of the Rules for Studies (Tests) for Evaluation of Biological Action of Medical Products On Approval of Rules for Technical Testing of Medical Products On Approval of Rules for the Monitoring of Safety, Quality and Efficacy of Medical Products On Special Trademark of Circulation of Medical Products in the Market of the Eurasian Economic Union On Approval of the Procedure for Application of Measures to Suspend or Prohibit Use of Medical Products Posing Threat to Human Life and (or) Health, Poor-Quality, Counterfeit and Falsified Medical Products by Authorized Authorities of Member States of the Eurasian Economic Union and their Withdrawal from Circulation in the Territories of Member States of the Eurasian Economic Union Page Rating Categories No categories were selected
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