Roszdravnadzor set aside 24 hours to remove Erespal from circulation. Medical activities Federal Service for Surveillance of Medicines

The company ROSZDRAVNADZOR 7710537160 is registered at the legal address 109074, MOSCOW CITY, SLAVYANSKAYA SQUARE, 4, 1. The company was registered on 04/12/2004. The organization was assigned the All-Russian State Registration Number: 1047796244396. The full name of the company is FEDERAL SERVICE FOR SUPERVISION IN THE FIELD OF HEALTH. According to the documents, the main type of activity is the Activities of federal government bodies, except for authorized representatives of the President of the Russian Federation and territorial bodies of federal executive bodies. The head is ACTING HEAD PARKHOMENKO DMITRY VSEVOLODOVICH. To obtain more detailed information, you need to go to the company’s card and check the reliability of the counterparty.

Interdistrict Inspectorate of the Federal Tax Service No. 46 for Moscow carried out registration with ROSZDRAVNADZOR on 04/12/2004. The registration procedure with the State Institution - Main Directorate of the Pension Fund of the Russian Federation No. 10 Directorate No. 2 for Moscow and the Moscow Region, Basmannoe Municipal District of Moscow, was started on March 31, 2006. Branch No. 20 of the State Institution - the Moscow Regional Branch of the Social Insurance Fund of the Russian Federation registered the company on 12/20/2016 00:00:00. In the Unified State Register of Legal Entities, the last entry about the organization has the following content: Change of information about the legal entity contained in the Unified State Register of Legal Entities.

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5.1.4. federal state supervision in the field of circulation of medicines (in relation to medicines for medical use) through:

5.1.4.1. organizing and conducting inspections of compliance by subjects of medicines circulation with the requirements established by the Federal Law "On the Circulation of Medicines" and other regulatory legal acts of the Russian Federation adopted in accordance with it for preclinical trials of medicines, clinical trials of medicines, storage, transportation, dispensing, sale of medicines means, use of medicines, destruction of medicines;

5.1.4.2. organizing and conducting inspections of the compliance of medicines in civil circulation with the established mandatory requirements for their quality;

5.1.4.4. application, in the manner established by the legislation of the Russian Federation, of measures to suppress identified violations of mandatory requirements and (or) eliminate the consequences of such violations, including making decisions on placing medicines for medical use in circulation, issuing orders to eliminate identified violations of mandatory requirements and attracting to the responsibility of persons who committed such violations;

Information about changes:

The regulation was supplemented by subclause 5.1.4.5 from November 27, 2019 - Decree of the Government of Russia of November 15, 2019 N 1459

5.1.4.5. conducting test purchases in order to verify compliance by subjects of medicines circulation engaged in retail trade in medicines for medical use with the rules for dispensing medicines for medical use and (or) prohibiting the sale of counterfeit medicines, substandard medicines and counterfeit medicines;

5.1.4(1). selective quality control of medicines for medical use through:

5.1.4(1).1. processing information mandatory provided by subjects of circulation of medicinal products for medical use on series and batches of medicinal products entering civil circulation in the Russian Federation;

5.1.4(1).2. sampling of medicinal products for medical use from subjects of circulation of medicinal products for medical use for the purpose of testing for their compliance with the requirements of regulatory documentation or regulatory documents;

5.1.4(1).3. making a decision based on the results of the tests on further civil circulation of the corresponding medicinal product for medical use;

5.1.4(1).4. making a decision on transferring a medicinal product for medical use to serial selective quality control of medicinal products for medical use in the event of repeated detection of non-compliance of the quality of a medicinal product for medical use with the established requirements and (if necessary) on checking the subject of circulation of medicinal products for medical use;

5.1.4(2). organizing and (or) conducting inspections of subjects of circulation of medicinal products for medical use for compliance with the rules of good laboratory practice, rules of good clinical practice, rules of good practice of storage and transportation of medicinal products, rules of good distribution practice, rules of good pharmacy practice;

5.1.6. control for:

5.1.6.3. implementation of regional programs for the modernization of healthcare in the constituent entities of the Russian Federation and measures to modernize state institutions providing medical care, government institutions implementing measures to introduce information systems in health care;

5.1.6.4. the reliability of primary statistical data provided by medical organizations and individual entrepreneurs engaged in medical activities;

Information about changes:

5.4.1. gives:

5.4.1.2. permission to import medical devices into the Russian Federation for the purpose of their state registration;

5.4.1.4. specialist certificate for persons who received medical or pharmaceutical education in foreign countries;

Information about changes:

The regulation was supplemented with subclause 5.4.1.5 from November 15, 2018 - Resolution

5.4.1.5. conclusion (permit document) for the import into the Russian Federation and export from the Russian Federation of samples of human biological materials (with the exception of human biological material obtained during a clinical trial of a medicinal product for medical use, and human biological material obtained during a clinical trial of a biomedical cellular product , for its study for the purposes of this clinical trial), hematopoietic stem cells, bone marrow, donor lymphocytes for the purpose of unrelated transplantation, germ cells and embryos;

Information about changes:

The regulation was supplemented by subclause 5.4.1.6 from November 15, 2018 - Decree of the Government of Russia of November 3, 2018 N 1315

5.4.1.6. conclusion (permit document) for obtaining a license for the right to import into the Russian Federation and export from the Russian Federation human organs and tissues, blood and its components (except for samples of human biological materials, hematopoietic stem cells, bone marrow, donor lymphocytes for the purpose of unrelated transplantation , germ cells and embryos);

Information about changes:

The regulation was supplemented by subclause 5.4.1.7 from November 29, 2019 - Decree of the Government of Russia of November 26, 2019 N 1510

5.5.1. maintains a state register of medical devices and organizations (individual entrepreneurs) engaged in the production and manufacture of medical devices, and places it on the official website of the Service on the Internet;

Information about changes:

Information about changes:

By Decree of the Government of the Russian Federation of January 31, 2017 N 114, the Regulations were supplemented with clause 5.7.1

5.7.1. Based on the results of monitoring the safety of biomedical cell products, publishes on its official website on the Internet information about the decision made to suspend the use of the biomedical cell product and (or) a related decision on the possible resumption of the use of the biomedical cell product;

5.8. carries out, in accordance with the established procedure, inspections of the activities of medical and pharmacy organizations, wholesale trade organizations of medicines, other organizations and individual entrepreneurs operating in the field of healthcare;

5.8.1. takes part, within the limits of competence, in maintaining federal information systems, federal databases in the field of healthcare, including ensuring the confidentiality of the personal data contained in them in accordance with the legislation of the Russian Federation;

Information about changes:

By Decree of the Government of the Russian Federation of September 6, 2014 N 913, the Regulations were supplemented with subclause 5.8.2

5.8.2. in case of detection of violations of the legislation of the Russian Federation on the circulation of medicines and in the field of health protection, issues mandatory instructions and holds them accountable for these violations, draws up protocols on administrative offenses and considers cases in accordance with the legislation of the Russian Federation on administrative offenses;

Information about changes:

By Decree of the Government of the Russian Federation of September 6, 2014 N 913, the Regulations were supplemented with subclause 5.8.3

5.8.3. publishes on the official website of the Service on the Internet information about scientific events, other events aimed at improving the professional level of medical workers or providing information related to monitoring the safety of medicinal products organized by organizations involved in the development, production and (or) sale of medicinal products preparations for medical use, organizations that have the rights to use the trade name of a medicinal product for medical use, wholesale trade organizations of medicinal products, pharmacy organizations, representatives of these organizations and (or) financed from the funds of these organizations and their representatives;

Information about changes:

By Decree of the Government of the Russian Federation of September 6, 2014 N 913, the Regulations were supplemented with subclause 5.8.4

5.8.4. forms a commission to resolve conflicts of interest in the implementation of medical activities and pharmaceutical activities;

Information about changes:

By Decree of the Government of the Russian Federation of September 6, 2014 N 913, the Regulations were supplemented with subclause 5.8.5

5.8.5. receives and records notifications about the start of activities in the field of circulation of medical devices (with the exception of conducting clinical trials of medical devices, their production, installation, adjustment, use, operation, including maintenance, and repair);

5.8.7. establishes the procedure for pharmacovigilance of medicinal products for medical use;

Information about changes:

By Decree of the Government of the Russian Federation of January 31, 2017 N 114, the Regulations were supplemented with subclause 5.8.8

5.8.8. establishes the procedure for monitoring the safety of biomedical cell products;

Information about changes:

By Decree of the Government of the Russian Federation of January 31, 2017 N 114, the Regulations were supplemented with subclause 5.8.9

5.8.9. establishes the procedure for the holders of registration certificates of biomedical cellular products, legal entities in whose name permits to conduct clinical trials of biomedical cellular products have been issued, or other legal entities authorized by them to receive, record, process, analyze and store biomedical cellular products received from subjects of circulation products and government authorities reports of side effects, adverse reactions, serious adverse reactions, unexpected adverse reactions when using biomedical cell products, the peculiarities of their interaction with drugs, medical devices, food products, other biomedical cell products, individual intolerance, and also about other facts and circumstances that pose a threat to human life or health or affect a change in the ratio of the expected benefit to the possible risk of using biomedical cell products;

5.9. carries out the functions of the main manager and recipient of federal budget funds allocated for the maintenance of the Service and the implementation of the functions assigned to it;

5.10. ensures, within its competence, the protection of information constituting state secrets;

5.11. organizes the reception of citizens, ensures timely and complete consideration of citizens' appeals, makes decisions on them and sends responses to applicants within the period established by the legislation of the Russian Federation;

5.12. organizes and ensures mobilization preparation and mobilization of the Service, manages the organization of activities for mobilization preparation and mobilization of its territorial bodies, as well as organizations whose activities are related to the activities of the Service or which are within the scope of its jurisdiction, have mobilization tasks or perform tasks for mobilization work;

5.17. performs other functions in the established field of activity, if such functions are provided for by federal laws, regulatory legal acts of the President of the Russian Federation or the Government of the Russian Federation.

6. In order to exercise powers in the established field of activity, the Federal Service for Surveillance in Healthcare has the right:

6.1. organize the necessary inspections, studies, tests, examinations, analyzes and assessments, as well as scientific research on the implementation of state control (supervision) in the established field of activity;

6.1.1. based on the results of monitoring the safety of medical devices upon receipt and confirmation of information about side effects not specified in the instructions for use or operating instructions for a medical device, undesirable reactions during its use, about the peculiarities of the interaction of medical devices with each other, about the facts and circumstances creating threat to the life and health of citizens and medical workers during the use and operation of registered medical devices, consider the issue of suspending the use or withdrawing such a medical device from circulation, make an appropriate decision and post information about the decisions made on the official website of the Service on the Internet;

6.11. create advisory and expert bodies (councils, commissions, groups, collegiums) in the established field of activity.

7. The Federal Service for Surveillance in the Sphere of Healthcare does not have the right to carry out legal regulation in the established field of activity, except in cases established by decrees of the President of the Russian Federation and decrees of the Government of the Russian Federation, as well as management of state property and the provision of paid services.

The restrictions on the powers of the Service established by the first paragraph of this clause do not apply to the powers of the head of the Service to manage the property of the Service assigned to it with the right of operational management, to resolve personnel issues and issues of organizing the activities of the Service.

III. Organization of activities

8. The Federal Service for Surveillance in the Sphere of Healthcare is headed by a director appointed and dismissed by the Government of the Russian Federation on the proposal of the Minister of Health of the Russian Federation.

The head of the Federal Service for Surveillance in Healthcare is personally responsible for the implementation of the tasks and functions assigned to the Service.

The head of the Federal Service for Surveillance in Healthcare has deputies who are appointed and dismissed by the Government of the Russian Federation on the proposal of the Minister of Health of the Russian Federation.

The number of deputy heads of the Service is established by the Government of the Russian Federation.

9. Head of the Federal Service for Surveillance in Healthcare:

9.1. distributes responsibilities among his deputies;

9.2. submits to the Minister of Health of the Russian Federation:

9.2.1. draft regulations on the Service;

9.2.2. proposals on the maximum number and wage fund of employees of the central office and territorial bodies of the Service;

9.2.3. proposals for the appointment and dismissal of deputy heads of the Service;

9.2.4. proposals for the appointment and dismissal of heads of territorial bodies of the Service;

9.2.5. draft annual plan and forecast indicators of the Service, as well as a report on their implementation;

9.2.6. proposals for the formation of a draft federal budget in terms of financial support for the activities of the Service;

9.2.7. proposals to submit for awarding state awards of the Russian Federation, Certificate of Honor of the President of the Russian Federation, Certificate of Honor of the Government of the Russian Federation, for encouragement in the form of a declaration of gratitude of the President of the Russian Federation, declaration of gratitude of the Government of the Russian Federation, for awarding a departmental insignia of the Ministry of Health of the Russian Federation, giving the right for the awarding of the title "Veteran of Labor" to employees of the central apparatus of the Service, its territorial bodies and subordinate organizations, as well as other persons carrying out activities in the established field;

9.3. appoints and dismisses employees of the central apparatus of the Service and deputy heads of its territorial bodies;

9.4. resolves, in accordance with the legislation of the Russian Federation on public service, issues related to the performance of federal public service in the Federal Service for Surveillance in Healthcare;

9.5. approves the structure and staffing table of the central apparatus of the Service within the limits of the wage fund and the number of employees established by the Government of the Russian Federation, the cost estimate for the maintenance of the central apparatus of the Service within the limits of the appropriations approved for the corresponding period and provided for in the federal budget;

9.6. approves the number and wage fund of employees of the territorial bodies of the Service within the limits established by the Government of the Russian Federation, as well as the estimated costs for their maintenance within the limits of the appropriations approved for the corresponding period provided for in the federal budget;

9.7. on the basis and in pursuance of the Constitution of the Russian Federation, federal constitutional laws, federal laws, acts of the President of the Russian Federation, the Government of the Russian Federation and the Ministry of Health of the Russian Federation, issues orders on issues within the competence of the Service.

10. Financing of expenses for the maintenance of the central apparatus and territorial bodies of the Federal Service for Surveillance in Healthcare is carried out from funds provided in the federal budget.

11. The Federal Service for Surveillance in Healthcare is a legal entity, has a seal with the image of the State Emblem of the Russian Federation and with its name, other seals, stamps and forms of the established form, as well as accounts opened in accordance with the legislation of the Russian Federation.

The Federal Service for Surveillance in Healthcare has the right to have a heraldic sign - an emblem, a flag and a pennant, established by the Ministry of Health of the Russian Federation in agreement with the Heraldic Council under the President of the Russian Federation.

12. The location of the Federal Service for Surveillance in Healthcare is Moscow.

The Federal Service for Surveillance in Healthcare (Roszdravnadzor) was formed in accordance with Decree of the President of the Russian Federation dated March 9, 2004 No. 314 “On the system and structure of federal executive authorities” and is a federal executive body exercising control and supervision functions in healthcare sector.

Roszdravnadzor is under the authority of the Ministry of Health of the Russian Federation and is guided in its activities by the Constitution of the Russian Federation, federal constitutional laws, federal laws, acts of the President of the Russian Federation and the Government of the Russian Federation, international treaties of the Russian Federation, acts of the Ministry of Health of the Russian Federation, as well as the Regulations “On the Federal service for supervision in the field of healthcare", approved by Decree of the Government of the Russian Federation of June 30, 2004 No. 323.

The Service carries out its activities directly and through its territorial bodies in interaction with other federal executive authorities, executive authorities of the constituent entities of the Russian Federation, local government bodies, public associations and other organizations.

Currently, the structure of the Federal Service for Surveillance in Healthcare includes the central apparatus (10 departments), 78 territorial bodies in the constituent entities of the Russian Federation and 3 federal state budgetary institutions.

Roszdravnadzor exercises the following powers:

1. State control:

For circulation of medical products;

Quality and safety of medical activities through inspections;

When handling medications:

For the application of prices for medicines included in the list of vital and essential medicines;

For the implementation of regional programs for the modernization of healthcare in the constituent entities of the Russian Federation and measures for the modernization of government institutions providing medical care, government agencies implementing measures to introduce information systems in healthcare;

The reliability of primary statistical data provided by medical organizations and individual entrepreneurs engaged in medical activities.

2. Control and supervision of the completeness and quality of implementation by public authorities of the constituent entities of the Russian Federation of the authority delegated to them to make annual cash payments to persons awarded the “Honorary Donor of Russia” badge, with the right to send orders to eliminate identified violations, as well as to hold officials accountable persons performing duties in the exercise of delegated powers.

3. Conducts:

Monitoring the range and prices of vital and essential drugs (VED);

Monitoring the safety of medical products, registration of side effects, undesirable reactions when using medical products, facts and circumstances that create a threat of harm to the life and health of people when handling registered medical products.

4. Carries out licensing of certain types of activities within the competence of the Service.

5. Outputs:

Permission for transit through the territory of the Russian Federation of potent substances that are not precursors to narcotic drugs and psychotropic substances;

Permission to import medical devices into the Russian Federation for the purpose of their state registration;

Certificate for the right to import (export) narcotic drugs, psychotropic substances and their precursors;

Specialist certificate for persons who received medical or pharmaceutical education in foreign countries.

6. Carries out state registration of medical devices;

7. Maintains the state register of medical devices and organizations engaged in the production and manufacture of medical devices;

8. Posts information on decisions made based on the results of drug safety monitoring;

9. Inspects the activities of organizations operating in the field of healthcare;

10. Organizes the reception of citizens, ensures timely and complete consideration of citizens’ appeals;

11. Performs other functions regulated by the Regulations on Roszdravnadzor, as well as functions provided for by federal laws, regulatory legal acts of the President of the Russian Federation or the Government of the Russian Federation.