Національний юридичний університет імені Ярослава Мудрого ⚖ Головна ⓘ Довiдка
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1.

Вид документа : Статья из журнала
Шифр издания : PMID: 35029561/S53
Автор(ы) : Shevchuk, Viktor M., Parfylo, Ihor V., Sokolenko, Mykyta O.
Заглавие : Falsification of medicines and distribution of falsified medicines in ukraine: criminalistic means of detection and counteraction
Место публикации : Wiadomosci lekarskie. - 2021. - Vol. 74, Iss. 11, cz. 2. - P.2946-2953
УДК : 343.98:343.347
Ключевые слова (''Своб.индексиров.''): criminalistic characteristics--falsification of medicines--methods of investigation--optimization of investigation--tactical operation--криміналістичні характеристики--фальсифікація ліків--методи розслідування--оптимізація розслідування--тактична операція--криминалистические характеристики--фальсификация лекарственных средств--методи розслідування--оптимізація розслідування--методы исследования--оптимизация расследования--тактическая операция
Аннотация: OBJECTIVE: The aim: To formulate criminalistic recommendations to increase the effectiveness of combating falsification and contribution of falsified medicines. To accomplish analyze of the current state and trends in combating this criminal offense, to create the basis of criminalistic characteristics and methods of their investigation, taking into account the results of the generalization of judicial investigative practice and foreign experience. PATIENTS AND METHODS: Materials and methods: The examine and analysis of results and generalization of 128 criminal proceedings of such criminal offenses, court decisions for the period 2012- 2020; questionnaires of practical workers (205 people); results of generalization and analysis of published materials of investigative and judicial practice; foreign experience in combating falsification of medicines, etc. In the process of conducting this research, general scientific and special research methods were also used. RESULTS: Results: Based on the results of the generalization of investigative and judicial practice, a criminalistic description of falsification and contribution of falsified medicines in the form of descriptive and statistical information model has been developed, its elemental composition was determined and analysed. Reasonable that in theoretical terms criminalistic characteristics are the basis for building appropriate criminalistic methods, and in practical terms is considered as a kind of guideline that can be successfully used by investigators in the conduct of specific criminal proceedings, which allows choosing the most effective directions and means of investigation. CONCLUSION: Conclusions: One of the priority areas of research in criminalistics is the development of criminalistic characteristics and basics of investigation methods of falsification and contribution of falsified medicines, which must be carried out on the basis of the modern general theory of criminalistics, current legislation and practice, results of generalizationand analysis of investigator of judicial practice and foreign experience.
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Вид документа : Статья из журнала
Шифр издания : 346.548/K85
Автор(ы) : Krynytskyi, Igor Y, Noha, Petro P., Sarana, Serhii V.
Заглавие : Serialization as new quality control system of medicinal products
Место публикации : Wiadomosci lekarskie. - 2019. - Vol. 72, Issue:12 cz 2. - P.2473-2477
УДК : 346.548
ББК : Р11
Ключевые слова (''Своб.индексиров.''): quality of medicinal products--якість лікарських продуктів--качество лекарственных продуктов--falsified medicinal products--фальсифіковані лікарські препарати--фальсифицированные лекарственные препараты--medicinal products--лікарська продукція--лекарственная продукция--serialization--сериализация--серіалізація
Аннотация: OBJECTIVE: Introduction: medicinal products are special goods which the quality of life and health of the population directly depends on. Therefore, ensuring the quality of medicinal products is central to state policy of developed countries in the conditions of free movement of goods and services. High quality of medicinal products should be supported in the context of pharmaceutical market globalization by using exclusively a modern quality control system such as serialization. The aim: the rationale for the need to use the serialization system of medicinal products by European countries which are not a part of the EU is the goal of our research. PATIENTS AND METHODS: Materials and methods: the research is based on EU law (Directive 2001/83/EC, Directive 2011/62/EU, Delegated Regulation (EU) 2016/161), Ukrainian legislation, statistics of WHO, General Prosecutor's Office, European Union Intellectual Property Office, Court judgment of the Ukrainian courts, legal doctrine in the field of medical law. The research is also based on general and special scientific research methods. CONCLUSION: Conclusions: existing quality control mechanisms do not cope with the task of providing the people with access to high quality and safe medicinal products. The serialization of medicinal products provides an opportunity to raise the quality control of medicinal products to a new level in the process of globalization. Serialization of medicinal products is important for Ukraine and other country's not in EU, it will fill the internal pharmaceutical market with a qualitative product and will allow the export of medicinal products.
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Вид документа : Статья из журнала
Шифр издания : 6/P30
Автор(ы) : Pashkov, Vitalii M., Soloviov, Aleksey, Olefir, Andrii
Заглавие : Legal Aspects of Counteracting the Trafficking of Falsified Medicines in the European Union
Место публикации : Wiadomosci lekarskie. - 2017. - Vol. 70, Issue:4. - P.843-849
УДК : 6
ББК : Х623.211.84
Ключевые слова (''Своб.индексиров.''): директива 2001/83 / ec--положение (ес) 2016/161--подделка--уголовная ответственность--фальсифицированные наркотики--некачественные препараты--уникальный идентификатор
Аннотация: INTRODUCTION: The paper identifies key risks associated with the illegal production and sale of medicines. Also there were generalized features of criminal responsibility for acts related to the trafficking of drugs in some Member States of the EU and analyzed legal means of combating the falsified drugs today. The problem concerning falsification of medicines is particularly acute not only in developing countries but also in developed ones. Fake is one in ten - twenty drug. The largest share of falsified drugs comes from the so-called «Asian tigers», already from which they come to the EU market. THE AIM: In this publication authors have set following objectives: - to determine the risks associated with illegal production and sale of medicines; - organize legal means of combating the falsified medicines in the EU member states; - clarify features of criminal responsibility for acts related to the trafficking of drugs in the EU countries. MATERIALS AND METHODS: The article bases on the works of scholars and experts, statistical information and other sources. Particular attention is paid to the analysis of regulations of the EU institutions and national criminal laws. So, provisions of the criminal codes of 10 EU member states were taken into account. RESULTS: There is a system of legal measures which counter the circulation of falsified medicines in the EU and consists of general and specific regulatory requirements, mainly of economic and legal nature. The most important role among the last play package labeling requirements for drugs and license conditions. DISCUSSION: In the article were discussed factors that stimulate the production and sale of falsified drugs and the risks associated with these. Demarcated the concept of «falsified medicinal product», «counterfeit drug», «substandard drug». CONCLUSIONS: Although there are guidelines for patients to identify falsified drugs, still a major role in this process should play public authorities and enterprises. In all the countries illegal circulation of falsified drugs is prohibited under threat of criminal or administrative responsibility.
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Умовні позначення місця знаходження

3_пов.(ЗПІ) – зала правової інформації, НБК

4_пов.(НАб) – абонемент наукової літератури, НБК

4_пов.(ДБФ) – довідково-бібліографічний фонд, НБК

5_пов.(З/П) – зала періодичних видань, НБК

6_пов.(АХЛ) – абонемент художньої літератури, НБК

6_пов.(ЗІЛ) – зала літератури іноземними мовами, НБК

7_пов.(Хр) – книгосховище, НБК

8_пов.(РК) – книгосховище рідкісних видань та дисертацій, НБК

НБВ – інформаційно-бібліографічний відділ, НБК, 7 поверх

Ст.Аб. – студентський абонемент, НБК, 5 поверх

Філ №1 – філія № 1 (вул. Динамівська, 4)

Філ №2 – філія № 2 (вул. Пушкінська, 106)

Полт. фак. – Полтавський юридичний інститут, м. Полтава