(<.>K=ЛІКАР$<.>)

Vilchyk, T. B..
    Areas for further improvement of legislative regulation of patients' rights in Ukraine [Text] / T. B. Vilchyk, A. K. Sokolova // Wiadomosci lekarskie. - 2019. - Vol. 72, Iss. 7. - P. 1324-1330
   Перевод заглавия: Направления дальнейшего совершенствования законодательного регулирования прав пациентов в УкраинеББК Х620.321 + Х623.211.84 + Р11

Аннотация: OBJECTIVE: Introduction: The article reviews issues of legal regulation of patients' rights in Ukraine, analyzes the patient-doctor relationship, proposes the legislative approval of new patients' rights and the need of adoption of a single legislation of these rights. The aim of this work is to conduct a detailed study of legal regulation of patients' rights in Ukraine and the EU countries, to identify the areas for further improvement of the legislative regulation of patients 'rights in Ukraine, ways of harmonization of national legislation with international standards, which regulate patients' rights. PATIENTS AND METHODS: Materials and methods: we analyzed national and international regulation of patients' rights, case law of the European Court of Human Rights (ECHR), national court judgments. We also used historical, comparative-legal methods, and instruments of analytical research and empirical study. CONCLUSION: Conclusions: In Ukrainian law many patient rights are not defined, but are applied in medical practice, therefore, they require legal regulation. In particular, they include: the right to convene a consilium; the right to refuse medical interference; the right to terminate treatment, etc. In addition, with the development of medicine, scientific and technological progress, there are some issues, which arise and need to be legally defined, among them: the rights and responsibilities of the patient during transplantation, artificial insemination, medical research, etc. When making health policy, the concept of trust and respect for patients, their autonomy or constructive partnership with them should be taken into account. Doctors need to take a more active part in discussions and debates with patients. Independence of patients in decision making processes must be provided by law, and the rights and obligations of all parties must be clearly reflected in the relevant documents.

Анотація - 0 байт

Baulin, Yu. .
    Legal regulation of professional obligations of physicians in Ukraine [Текст] / Yu. Baulin, B. Rohozhyn, I. Vyshnevska // Wiadomosci Lekarskie. - 2019. - Vol. 72, Iss. 9. - p. 1839-1843
   Перевод заглавия: Правовое регулирование профессиональных обязанностей врачей в УкраинеББК Х628.111.3

Аннотация: OBJECTIVE: Introduction: It was identified that one of the priorities of medical reform in Ukraine is the establishment of an effective system of legal regulation of professional physician's obligations that meets European standards. However, the legal regulation of relations between actors in the field of health care lags behind the practice of their development. The aim to find out the status of legal regulation of the professional obligations of health workers, to identify the gaps in this regulation, to formulate proposals for improving the legal framework for the issue under investigation. PATIENTS AND METHODS: Materials and methods: Legislation of Ukraine and certain European countries, international declarations and conventions, scientific works, 28 judgments of the European Court of Human Rights, 96 sentences of the practice of the national courts of Ukraine. CONCLUSION: Conclusions: During the study, the stages of determining the professional physician's obligations were singled out, which would optimize the legislative process of regulation of obligations. One of the problems is the incorrect translation of protocols, which is assigned to a medical care institution. It was proposed to solve this problem by introducing a unified system of protocols and standards, the duty of translation and adaptation of which is entrusted to the central body of executive power in the field of health care. It is relevant to consolidate the duty of medical records management at the level of law, which will serve as a guarantee of ensuring the proper performance by the physician of a professional obligation to treat and diagnose a particular patient. In order to avoid cases of judgments, based on the results of the сommission's assessment of the actions of a physician and to eliminate the number of cases of unjustified attraction of physicians to liability, it is necessary to consolidate a clear list of general professional physician's obligations in a single regulatory act.

Анотація - 0 байт
, Работа с электронной копией документа возможна только в читальном зале библиотеки
, Работа с электронной копией документа возможна только в читальном зале библиотеки

Shul'ha, M. G.
    Legal regulation of importation of medicinal products: european standards and national practice [Text] / M. G. Shul'ha, A. V. Mazur, I. V. Georgiievskyi // Wiadomosci lekarskie. - 2019. - Vol. 72, Iss. 12, cz. 2. - p. 2457-2463
   Перевод заглавия: Правовое регулирование ввоза лекарственных средств: европейские стандарты и национальная практикаББК Х621.154.2
РУБ DOI: 10.36740/WLek201912211

Аннотация: OBJECTIVE: Introduction: The state policy in the field of medicinal products supply and import adjustment is aimed at steady assurance of quality throughout all stages of medicinal products circulation, starting with production and import to the stage of their medical application. The aim:of the article is to study the existing permitting and restrictive legal mechanisms of importing medicinal products at international, regional and national levels. PATIENTS AND METHODS: Materials and methods: This research is based on empirical and analytical data from the WHO, EU, EU customs and medical legislation, national legislation of Ukraine and Republic of Poland, Eurostat statistics, European Court of Justice (hereinafter referred to as ECJ) rulings. CONCLUSION: Conclusions: Customs regime prohibitions and restrictions are of particular importance when it comes to importing medicinal products. That specificity is in the procedures of licensing, certification, quality control, packaging, marking etc. A proper mechanism for carrying out such procedures requires standardization at international and regional levels. At the level of regional cooperation the issue of parallel import of medicinal products is urgent. Associated risks should be minimized by means of the instruments of international, European law through the adaptation of the national licensing procedures of medicinal products import to the EU requirements, including those defined in the Association Agreements.

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Krynytskyi, I. Y..
    Serialization as new quality control system of medicinal products [Текст] / I. Y. Krynytskyi, P. P. Noha, S. V. Sarana // Wiadomosci lekarskie. - 2019. - Vol. 72, Issue:12 cz 2. - P. 2473-2477
   Перевод заглавия: Сериализация как новая система контроля качества лекарственных средств

УДК

346.548

ББК Р11
РУБ DOI: 10.36740/WLek201912213

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.

Текст - 0 байт

Shevchuk, V.
    Testing of drugs in the implementation of customs control in Ukraine: legal aspects [Текст] = Экспертиза лекарственных наркотических средств при осуществлении таможенного контроля: правовой аспект / V. Shevchuk, O. Shevchuk, N. Matyukhina, D. Zatenatskyi, O. Chub // Georgian medical news. - 2020. - Issue: 1(298). - P. 165-169

УДК

343.575

ББК Х628.112.030

Аннотация: The purpose of the study is to analyze certain aspects of the legal regulation of the examination of medicines containing narcotic drugs, psychotropic substances, or precursors in the field of customs. To achieve this goal, we analyzed the number of customs examinations carried out, new narcotic compounds identified for the first time. An analysis of the understanding of the definition "examination" and "customs examination" in the scientific literature. Two directions of the implementation of expert examinations of medicines containing narcotic drugs, psychotropic substances, or precursors in the field of customs were identified, its concept was defined. It is proposed to attribute the investigative examination to the methods of customs control. It was found out that this examination is not a forensic examination, and it can be attributed to a special class of examinations, since it has characteristic features inherent only in it: subject, tasks, objects, and research methods. Seven stages of the implementation of expert examinations of medicinal products containing narcotic drugs, psychotropic substances, or precursors during customs control are highlighted and their procedural order is analyzed.

Текст - 0 байт
, Работа с электронной копией документа возможна только в читальном зале библиотеки

Horbachova, K.
    The right on euthanasia: The experience of the world's developed countries and the prospects of its implementation in Ukraine [Text] / K. Horbachova, V. Dudaryov, Zarosylo V., Baranenko D., Us O. // Journal of Legal, Ethical and Regulatory Issues. - 2020. - Vol. 23, Iss. 1. - p. 1-6
   Перевод заглавия: Право на эвтаназию: опыт развитых стран мира и перспективы его внедрения в УкраинеББК Х628.111.3

Аннотация: The article explores the right on euthanasia in developed countries of the world and the prospects for its implementation in Ukraine. The results of a number of sociological studies on the perception of euthanasia by the population, in particular in the Netherlands, Turkey, USA, Finland, also, special attention was paid to the gradual increasement in the percentage of people who support the idea of euthanasia. The concept of euthanasia and the conditions under which it can be carried out are revealed. The legislative provisions of the Netherlands and Belgium regulating euthanasia in these countries were stated. It has been found out that the shortage of consensus among European states on the question of a decent end to human life leads to the existence of a case law of the European Court of Human Rights on euthanasia cases. It is concluded that the introduction of euthanasia is not promising for Ukraine, as it is directly contrary to a number of national legislation acts, first of all the Constitution of Ukraine, also, to international acts, in particular the Convention for the Protection of Human Rights and the Founder of Freedoms. It is emphasized that a single position on euthanasia should be chosen at the level of the European Union by the Member States.

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Ovcharenko, Е. .
    Проблемы правовой защиты наркозависимых лиц, которые получают заместительную поддерживающую терапию: опыт Луганского региона в сравнительном аспекте [Text] = The Problems of Legal Protection of Drug Addicts, who Receive substitution Maintenance therapy: ukrainian experience / Е. Ovcharenko, N. Ovcharenko, O. Shekera // Psychiatry, Psychotherapy and Clinical Psychology. - 2019. - Vol. 10, Iss. 2. - p. 319-332 ББК Х629.08

Аннотация: In the article, there are analyzed legal aspects of organization of substitution maintenance therapy in medical institutions of Ukraine, taking into account universally recognized world standards. Experience of implementation of the program of substitution maintenance therapy in Lugansk region demonstrated visible positive results in treatment of injecting drug users and identified the key problematic issues. The main challenges include the following: lack of access to legal protection for drug addicts, imperfection of current legislation, problems in the relationships with social surrounding (relatives, state institutions). It was proved that the integrated approach to solving problems of patients, who receive substitution maintenance therapy, which combines medical, social and legal components, should be universally introduced. There were formulated the proposals aimed to amend the relevant legislation, regulating organization of specialized medical and legal assistance to drug addicts.

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Korcheva, T.
    Врачебная тайна: медицинский, уголовно-процессуальный и философско-правовой аспекты ее разглашения (обзор) [Text] = Medical privacy: medical, criminally-remedial and the philosopho-legal aspects of its disclosure (review) / T. Korcheva, E. Nevelskaia-Hordeeva, D. Voitenko // Georgian medical news. - 2020. - Issue:306. - P. 166-171

УДК

342.746

ББК Х623.211.84

Аннотация: The purpose of the study is to determine the subject of "medical secrecy", to characterize the subjects who are obliged to keep secret information that is the subject of medical secrecy and, based on the results of this study, to make author's proposals to clarify the name for confidential medical information in legislation in the field of medicine in the field of medicine, criminal and criminal procedural legislation. The article explores issues related to the right of every person to the confidentiality of medical information, which is legally defined as "medical privacy". Based on the analysis of international legal acts, decisions of the European Court of Human Rights, the legislation of Ukraine and Georgia on the researched subject, using the foundations of the philosophy of law, carried out a comprehensive study of the concept of "medical confidentiality", defined entities following their professional and career responsibilities, must keep it. In the given article were used such scientific methods as logical, system-structural, comparative-legal, analysis, synthesis. Based on the research, the authors make several proposals for improving certain norms governing medical activities, namely, changes to the wording of Article 40 of the Law of Ukraine "Fundamentals of Ukrainian Legislation on Health Protection", Article 145 of the Criminal Code of Ukraine and Article 65 of the Criminal Procedure Code of Ukraine.

Текст - 0 байт
, Работа с электронной копией документа возможна только в читальном зале библиотеки

Demura, M. I..
    Challenges of health care professionals' disciplinary and criminal prosecution [Текст] / M. I. Demura, V. A. Kononenko, N. A. Fedosenko // Wiadomosci lekarskie. - 2020. - Vol. 73, Iss. 12. cz. 2. - P. 2827-2832
   Перевод заглавия: Проблемы дисциплинарного и уголовного преследования медицинских работниковРУБ PubMed ID33611289

Аннотация: OBJECTIVE: The aim of the research is to study the peculiarities of the legislative consolidation of criminal and disciplinary liability for offenses of health care professionals in Ukraine and other states. PATIENTS AND METHODS: Materials and methods: Criminal legislation of Ukraine, international acts, decisions of the European Court of Human Rights (hereinafter - ECHR), data of the Integrated State Register of Judgments, as well as criminal legislation of Germany, the French Republic, the Kingdom of Denmark, the Republic of Belarus, Kazakhstan and many other countries. A set of general and special scientific methods of scientific knowledge was the methodological basis. The use of the comparative law method has become useful in the analysis of Ukrainian legislation and the legislation of other states. CONCLUSION: Conclusions: the article examined the features of the legislative consolidation of criminal and disciplinary liability for offenses of health care professionals in Ukraine and other countries. A comparative legal analysis of the legal enshrinement of the corpus delicti in the form of non-performance or misconduct of professional duties by a health care or pharmaceutical worker was carried out on the example of Ukraine and many other countries; types of penalties for medical crimes, which are established for this type of offense, were identified; sanctions for committing a disciplinary misconduct by a health care professional were determined on the example of the legislation of different countries.

Текст - 0 байт
, Работа с электронной копией документа возможна только в читальном зале библиотеки

Borysov, V. I..
    Special features of the legal status of the research subject in clinical testing of medicines [Текст] / V. I. Borysov, O. I. Antoniuk, I. I. Vyshnyvetskyy // Wiadomości Lekarskie. - 2019. - Vol. 72, Iss. 12, cz. 2. - P. 2464-2472
   Перевод заглавия: Особливості правового статусу суб’єкта дослідження при клінічному випробуванні лікарських засобів

УДК	347.121:61

РУБ PubMed: 32124770 + DOI: 10.36740/WLek201912212

Аннотация: The issue of the content of the legal status of the research subject in clinical testing of medicines and its distinction from the patient's legal status is of practical importance, related to the observance of ethical standards in the field of clinical trials, as well as ensuring the balance of public and private interests in this field. Although the subject of this study and the patient being treated are usually united in the intention to overcome the disease, these processes have different essence. The regulation of the legal status of the research subject should be done by legal means that are relevant to the nature of such trials and ensure the effective protection and security of the interests of these subjects. Normative regulation of the legal status of the research subject, unlike the patient, is insufficiently structured and characterized by fragmentation thus requires the doctrinal elaboration. The aim: The aim is to determine specific features of the legal status of the research subject and its difference from the patient's legal status being provided with medical care; to reason about the necessity and content of propositions to amend the current legislation of Ukraine in order to ensure the rights and legitimate interests of the research subjects. PATIENTS AND METHODS: Materials and methods: The authors used the judgements of the European Court of Human Rights (ECHR) on medical research, international and national regulatory acts, publications of scholars in the field of medical law. The research was carried out on the basis of the systematic approach using the methods of dialectical and formal logic, general scientific and specific legal methods of research. CONCLUSION: Conclusions: With the aim to ensure the proper legal protection of the rights and legal interests of the subjects of clinical trials the authors provided arguments for the need to amend the current legislation of Ukraine in order to correspond the international legal acts and ethical standards.

Текст - 0 байт
, Работа с электронной копией документа возможна только в читальном зале библиотеки

Borysov, V. I..
    Peculiarities of legal responsibility for offenses in the field of clinical trials of medicines [Текст] / V. I. Borysov, O. I. Antoniuk, O. O. Pashchenko // Wiadomosci Lekarskie. - 2020. - Vol. 73, Iss. 12, Part 2. - P. 2833-2839
   Перевод заглавия: Особливості юридичної відповідальності за правопорушення у галузі клінічних випробувань лікарських засобів

УДК

343.6:615

РУБ DOI: 10.36740/WLek202012222

Аннотация: OBJECTIVE: The aim: Is to determine the features of legal liability for violations in the field of clinical trials of medicine remedies and justification of proposals to strengthen the protection of participants' interests in clinical trials through the use of various types of such liability. PATIENTS AND METHODS: Materials and methods: The authors used the decisions of the European Court of Human Rights (ECHR) on medical research, international and national regulations, and publications of scholars in the field of medical law. The research was carried out on the basis of a systematic approach using the methods of dialectical and formal logic, general scientific and special legal research methods. CONCLUSION: Conclusions: In order to properly ensure the legal protection of public interests, as well as the rights and interests of research subjects and other entities involved in their implementation, the authors argue the need to use different types of legal liability.

Текст - 0 байт
, Работа с электронной копией документа возможна только в читальном зале библиотеки

Prudnykova, O. V..
    European Court of Human Rights as a guarantee of observation the medical secrecy [Текст] / O. V. Prudnykova, V. M. Pyvovarov, O. V. Fedosova, O. A. Stasevska, O. V. Umanets // Journal of Forensic Science and Medicine. - 2021. - Vol. 7, Iss. 4. - P. 145-151
   Перевод заглавия: Європейський суд з прав людини як гарантія дотримання лікарської таємниці

УДК	341.231.14

РУБ DOI: 10.4103/jfsm.jfsm_70_21

Аннотация: The European Convention on Human Rights proclaims the right of everyone to privacy of information about their state of health, which is a particularly important issue during the COVID-19 pandemic. The aim of the study is to determine the essence of the ECtHR's activity as a guarantee of information culture, highlight the main elements of its activities in this aspect, and analyze the right to medical secrecy in the practice of the European Court of Human Rights. The formal-logical method was used to analyze the norms of the European Convention on Human Rights, determine the content of basic concepts, and systematize the material in order to obtain generalizing conclusions within the framework of the stated problem. The predictive method was used to determine the prospects for the development of legislation aimed at creating a system of effective legal provision for the confidentiality of patient information. The European Court of Human Rights has more than once drew attention to the enormous importance of protecting personal, in particular medical data, so that a person can enjoy his or her right to private and family life with satisfaction. That is why public authorities must ensure the confidentiality of information about the health of individuals. It should not be disclosed or processed without the prior informed consent of the person concerned. There are a lot of cases of unlawful disclosure of information about the patient's health and liability for unlawful disclosure.

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Ponomarenko, O. M..
    Legal regulation of the "biological" protection of marriage and family: issues of balancing between the right to medical secret and the right to conscious marriage [Текст] / O. M. Ponomarenko, Y. A. Ponomarenko, K. Yu. Ponomarenko // Wiadomosci lekarskie. - 2021. - Vol. 74, Iss. 11, cz. 2. - P. 3009-3015
   Перевод заглавия: Правове регулювання «біологічного» захисту шлюбу та сім'ї: питання балансування між правом на лікарську таємницю та правом на свідомий шлюб

УДК

347.6

РУБ DOI: 10.36740/WLek202111225 + PMID: 35029571

Аннотация: OBJECTIVE: The aim: The purpose of this article is to analyze the state policy of several states in creating an effective mechanism in which persons entering into marriage will be able to obtain the necessary information about the state of each other's health and thereby make an informed decision about registering a marriage, protecting the health of each other and future offspring. PATIENTS AND METHODS: Materials and methods: In the course of the study, a comparative analysis of the legal means used by some states in the field of biological protection of marriage was carried out. First of all, a study was carried out of the family legislation of states with different approaches to the system of premarital medical examination of persons entering into marriage. In addition, the scientific works of scientists from different countries were used, the object of study of which was the problems associated with the biological protection of marriage. The work also used the results of surveys that were conducted in some countries and highlighted in published scientific works. CONCLUSION: Conclusions: Health information is essential when deciding whether to marry. Hiding such information can seriously harm the partner's health and children born in such a union. The task of the state is to find a middle ground, in which the balance of interests of the person, whose medical examination revealed health problems (the right to medical secrecy), on the one hand, and the person with whom it is planned to register a marriage (the right to health protection; the right on the voluntariness of marriage).At the same time, the emphasis in state policy on the biological protection of the family should be placed on preventive measures, including non-legal means of information.

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Логвиненко, Б. А.
    Противодействие корупции при государственных закупках лекарственных средств [Text] = Counteraction to corruption during public procurement of medicinal products / Б. А. Логвиненко, А. М. Подоляка, Ю.М. Дьомин, И. А. Колесникова, К. А. Салаева // Georgian Medical News. - 2022. - Iss. 323, No. 2 [не зазначено у Scopus та Web of Science]. - P. 175-179

УДК

343.9

РУБ PMID: 35271492

Аннотация: The purpose of the article is to carry out a comparative analysis of common manifestations of corruption and corruption risks during public procurement of medicinal products in Ukraine and foreign countries in order to find effective ways to counteract to such cases. The materials of the research were the provisions of foreign legislation, national regulatory legal acts in the health care sector. Theoretical basis of the article is research focused on various aspects of combating corruption in the field of medicine, ways to prevent and minimize cases of corruption manifestations, improvement of anti-corruption measures during public procurement of medicinal products. The authors of the article have used comparative, comparative and legal, historical and legal, formal and legal methods, methods of formal logic, method of system analysis. It has been concluded that the problem of corruption is not new for public procurement area. However, corruption risks increase significantly during emergency situations. Public procurement of medicinal products is an extremely important and at the same time rather prone procedure to such risks. Threats of corruption manifestations during public procurement of medicinal products affect not only the country's economy, but also the indicators of the public health of the population, its working ability and vital function in the whole. The importance of the studied issue determines the need to strike a balance between the promptness of conducting the procurement of medicinal products, the preservation of anti-corruption measures and the effectiveness of response to emerging threats. Wide coverage of procedures of public procurement of medicinal products with the usage of electronic trading systems together with the demonstrativeness and accountability of such activities, can act as appropriate tools to prevent corruption manifestations. Taking into account the possible manifestations of corruption at each stage of public procurement is an important matter. It allows us to focus on counteraction measures and the proper response of the state to illegal actions.

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Зміст - 0 байт

Pashkov, V. .
    The Legal Nature of Managed Entry Agreements (MEAs) in the Coronavirus Response System [Текст] / V. Pashkov // Ukrainian Healthcare Law in the Context of European and International Law / Editors: R. Maydanyk, André den Exter, I. Izarova : Springer, 2022. - Vol. 7. - P. 261-276. - (European Union and its Neighbours in a Globalized World ; Vol. 7). - [Вказана інша організація - некоректна назва. Не в профілі Ун-ту ]
   Перевод заглавия: Правова природа угод про керований вступ (MEA) у системі реагування на коронавірус

УДК	347.77:[604.4:615.371]

РУБ DOI: 10.1007/978-3-031-05690-1_15

Аннотация: This article elaborates on the admission procedure for vaccines against COVID-19 in various European countries and the United States. Neither the EU countries nor the United States has applied for a full license to manufacture or issue a coronavirus vaccine registration certificate. At best, it is an emergency use authorization or conditional marketing authorization. A particular focus will be on the Legal Nature of Managed Entry Agreements (MEAs) in the Coronavirus Response System. The use of MEAs allows not only to legalize emergency use authorization or conditional marketing authorization as a way to combat coronavirus infection, but also others, including for treating, preventing, or diagnosing seriously debilitating or life-threatening diseases. That includes orphan medicines. However, Ukraine and Russia have followed the path of simplifying the registration and full admission of vaccines for further use. Russia registered vaccines against COVID-19 of its own development, however, in Ukraine, there is a situation when it fully legalizes vaccines against COVID-19 earlier than the countries of this vaccine’s origin. This is due to ignoring the regulations and the experience of using MEAs both by Ukraine and Russia. © 2022, The Author(s), under exclusive license to Springer Nature Switzerland AG.

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Scopus - 0 байт

Shevchuk, V. M..
    Criminal offences related to illicit trafficking in falsified medicines: investigation problems [Електронний ресурс] / V. M. Shevchuk, O. L. Musiienko, M. O. Sokolenko // Wiadomosci Lekarskie. - 2023. - Vol. 76, Iss. 5. pt. 1. - P. 992-1000. - References : p. 998-1000
   Перевод заглавия: Кримінальні правопорушення, пов’язані з незаконним обігом фальсифікованих лікарських засобів: проблеми розслідування

УДК

343.347

РУБ DOI: 10.36740/WLek202305116 + PMID: 37326081

Аннотация: OBJECTIVE: The aim: Formulate recommendations for improving the efficiency of detection and investigation of trafficking in falsified medicines, application of criminalistics knowledge. To analise the contemporary condition and the latest trends in combating this type of crimes and to justify the need for creation of a complex criminalistic methodic investigation. PATIENTS AND METHODS: Materials and methods: Аnalysis of the applicable laws governing trade in medical products in Ukraine; judgments of courts of Ukraine for the period from 2013 to 2022; results of generalization of 128 criminal proceedings; active employee survey results (205 respondents) etc. Over the course of the present research, we have used general scientific and specialised research methods. RESULTS: Results and Conclusions: Increasing the effectiveness of combating the illegal circulation of falsified falsified medicines is a complex problem that encompasses a whole system of directions, requiring the combined efforts of international bodies and organizations, various scientists. One of the priority directions for the introduction of an effective mechanism for combating the distribution of falsified medicines is the development of a complex criminalistic methodic investigation.

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Scopus - 0 байт

Grynko, L. .
    Sale of falsified medicines via the internet in Ukraine: problems of detection and counteraction [Електронний ресурс] / L. Grynko, H. Chornyi, M. Kostenko // Wiadomosci Lekarskie. - 2023. - Vol. 76, Iss. 5. pt. 1. - P. 1106-1112. - References : p. 1110-1111
   Перевод заглавия: Продаж фальсифікованих ліків через інтернет в Україні: проблеми виявлення та протидії

УДК

343.347

РУБ DOI: 10.36740/WLek202305132 + PMID: 37326096

Аннотация: OBJECTIVE: The aim: The purpose of the article is to identify and analyze problematic theoretical and practical aspects related to the sale of counterfeit medicines via the Internet and measures to counteract the spread of their counterfeit products, as well as to search for evidence-based ways to improve the regulatory and legal mechanism that regulates the activities of the pharmaceutical business in Ukraine. PATIENTS AND METHODS: Materials and methods: The research based by the analysis of international acts, conventions and national legislation of Ukraine in the sphere of trade medicines via the Internet, scientific achievements in this area. Methodologically, this work is based on the system of methods, scientific approaches, techniques and principles with the help of which the realization of the research aim is carried out. There have been applied universal, general scientific and special legal methods. CONCLUSION: Conclusions: Analyzed the legal regulation of online sales of medicines. Made the conclusion about necessity implementation of projects to create forensic records which have shown their effectiveness in the fight against counterfeit medicines in European countries.

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