THE IMPACT OF THE INTRODUCTION OF ARTIFICIAL INTELLIGENCE TECHNOLOGIES ON THE CURRENT HUMAN RIGHTS AND FREEDOMS CONCEPT.

Artificial Intelligence (AI) has undeniably transformed the landscape of healthcare, offering unparalleled potential to enhance patient care, streamline diagnostics, and improve overall healthcare outcomes. As AI continues to make its way into the medical field, it has raised crucial questions about regulation, ethics, and patient safety and that is guiding us to the core question - how that will impact current human rights and freedoms concept, and is this concept ready for such an impact? The aim of the research is to identify and evaluate the potential impact of AI introduction in healthcare on modern human rights and freedoms concept, and on the basis of discovered complexities to propose ways to eliminate them. This study was conducted during June-October of 2023.

LEGAL CHARACTERISTICS OF PHARMACEUTICAL ACTIVITY UNDER THE EMERGENCY CONDITIONS: PANDEMIC AND WAR.

Objective: The aim: Study of the system of pharmaceutical activity legal support in emergency conditions, namely, the period of epidemics outbreak and during the war.

Patients And Methods: Materials and methods: In the mentioned study, we analyze the state of the governmental pharmaceutical policy during the pandemic and the war in Ukraine. Legal norms and doctrinal positions of scientists regarding the above-mentioned issue are studied.

ILLEGAL INTERNET PHARMACIES AS A THREAT TO PUBLIC HEALTH IN EUROPE.

Objective: The aim: This article aims to raise awareness and stimulate serious discussion about the dangers of illegal Internet pharmacies for patient safety and public health, the necessity to improve legal instruments, and unite the efforts of governments, professional organizations, and civil society for combating this activity.

Patients And Methods: Materials and methods: This study is based on the Medicrime Convention, empirical and analytical data of the WHO, Interpol, Europol, NABF, Directive 2011/62/EU of the European Parliament and of the Council of June 8, 2011, the regulatory acts and juridical practice of Ukraine, experts interview of pharmacy practicians, analysis of websites. Totally 18 laws and papers, 34 court judgments, 50 websites were analyzed, six experts were interviewed.

CHALLENGES OF CLASSIFICATION OF STAND-ALONE SOFTWARE AS A MEDICAL DEVICE.

Through a broad literature review, analysis of EU, USA, Ukraine regulation acts, scientific research, and opinions of progressive-minded people in this sphere, this paper provides a guide to understanding the essence of classification of stand-alone software with medical purpose and specifics of its regulation. This research is based on dialectical, comparative, analytic, synthetic, and comprehensive methods.

LEGAL MEANS OF ENSURING COMPETITION IN PHARMACY.

Objective: The aim: To research the consequences of pharmacy chains monopolization and establishment of legal means of neutralization of such consequences.

Patients And Methods: Materials and methods: The study is based on acts of the European Union, the United States, and Ukraine and international regulations and documents on health care. The study's materials were the results of a questionnaire survey of managers and specialists in a pharmacy on marketing contracts.

LEGAL REGULATION OF THE PROPER NATURAL ENVIRONMENTAL CONDITIONS AS AN INTEGRAL ENVIRONMENTAL HEALTH COMPONENT.

Objective: The aim: To investigate the legal basis for natural environmental protection as an integral environmental health component.

Patients And Methods: Materials and methods: In this work we study statutory regulations and scientific positions of scholars regarding above-mentioned issue. The study analyses generalized information from scientific journals by means of scientific methods from a medical and legal perspectives.

Falsification of medical products: criminal law mechanism combating threats to public health.

Objective: Introduction: Every civilized state has the duty to its citizens to create an effective health care system, a necessary component of which is the use of safe and high-quality medical products. This duty is based both on the standards of international law and national constitutional norms and principles. The spread of falsified medical products poses a global threat to public health, can lead to death or cause significant harm to human health.

Right to child health in context of natural environmental security.

Objective: Introduction: From different points of view, health in general and child health, in particular, constitute the highest value which preserves a significant amount of resource potential. Child health is understood as his/her state consisting of a certain system of elements (physical, psychological, etc.) each of which, on the one hand, is characterized by its specificity, and on the other hand, is in a complementary relationship with each other.

Improper healthcare marketing: German and Ukrainian experience in prevention.

Objective: Introduction: Improper healthcare marketing is a part of institutional corruption in the pharmaceutical markets, which causes significant harm to public health. Legal measures are an importent component of the mechanism for preventing this phenomenon. The aim: The purpose of the article is to raise awareness and stimulate serious discussion about the necessity to improve the preventative role of law in the field of healthcare marketing by adjusting liability for offenses in this area.