Law Policy Management,, and Regulation of Health
Shahriar eslamitabar
Volume 2, Issue 2 , February 2025, , Pages 1-16
Abstract
Background and Objective: Goods and services represent the two primary outputs of industry and economy, and ensuring their quality, safety and efficiency requires monitoring the production and supply processes. Given the critical importance of the health sector, this monitoring must be carried out accurately ...
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Background and Objective: Goods and services represent the two primary outputs of industry and economy, and ensuring their quality, safety and efficiency requires monitoring the production and supply processes. Given the critical importance of the health sector, this monitoring must be carried out accurately and in accordance with scientific standards; not only is an organizational duty, but also is a sovereign responsibility that would be applied by the governments as the custodians of public health.Methods: First, the literature of the article was reviewed using e-books, and articles, then the qualitative data was analyzed through content analysis and a practical model was presented.Results: Oversight of health services occurs in two general forms: 1- Supervision of service provider centers; 2- Supervision of specialists. Supervision of health products and goods is conducted by regulatory affairs specialists within each manufacturing company. The main regulatory body is the Food and Drug Administration of each country. The oversight and control utilize special tools such as providing guidelines and instructions, conducting inspections and enforcing regulations.Conclusion: Supervision should be done continuously in order to ensure the quality and safety of health goods and products. The services and goods possess fundamentally distinct natures. Firstly, services are not tangible to be fully observable and secondly, they are usually produced and delivered at the same time. Aboate the goods, monitoring is done continuously before and after entering the market by skilled experts, in order to prevent the entry of counterfeit and substandard products into the consumer market.
Law Policy Management,, and Regulation of Health
Shahriar eslamitabar
Volume 2, Issue 2 , February 2025, , Pages 31-41
Abstract
Background: good governance includes decision-making and implementation of important decisions, which are used in order to improve the efficiency of systems and different areas while promoting human rights. The elements and framework of governance have been seriously pursued by international institutions ...
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Background: good governance includes decision-making and implementation of important decisions, which are used in order to improve the efficiency of systems and different areas while promoting human rights. The elements and framework of governance have been seriously pursued by international institutions as a development tool in various fields, including health, in recent decades. Good governance can be achieved by emphasizing and paying attention to the principles of transparency, accountability, accountability, rule of law, participation, justice, efficiency and productivity, continuity and stability, frost and information and ethics. The principles of this governance, especially transparency, if implemented well, will also reduce administrative corruption. In the field of health, good governance improves the performance of the health system and, as a result, maintains and further improves the health of the society.Conclusion: With the movement towards globalization, the necessity of a single standards of good governance all over the world in order to strengthen the responsibility of governments is felt more and more. This standard is aimed at improving productivity with the secondary goals of fighting corruption, clarifying and realizing a healthy administrative system in the health sector. However, due to cultural and religious reasons, the realization of this world-inclusive standard in political and civil matters always faces serious resistance.
New Technologies Health and Law
Shahriar eslamitabar; MAHDI SAEIDIAN
Volume 2, Issue 2 , February 2025, , Pages 87-105
Abstract
Context and Purpose: France is known as the cradle of law and law. French e-Health in the field of health care have been compiled and approved based on the pillars and elements of the right to health introduced by the main international institutions of human rights and the World Health Organization and ...
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Context and Purpose: France is known as the cradle of law and law. French e-Health in the field of health care have been compiled and approved based on the pillars and elements of the right to health introduced by the main international institutions of human rights and the World Health Organization and according to the conditions and possibilities of the day. This field of new French laws with emphasis on electronic health can be a good model for the Islamic Republic of Iran in developing the aforementioned laws and regulations.Research Method: This article has been written using the paper and e-books and articles available in real and virtual libraries in a descriptive-explanatory method.Findings: The basics of health care law in of France, like any other country, include; The legal control of health care professionals is informed consent to treatment, negligence, error and confidentiality of personal information, which, although it has many similarities with the general trend of the world, is unique in its own way. The role of French public health law is also important in this regard. On the other hand, due to the fact that the right to independence and individual freedom is highly respected in France, an implicit or explicit contract between the mentioned specialists and the patient referred to them, in the form of civil rights and contract laws of France, is carefully considered. The legislator's attention has been drawn. From the beginning, these contracts will be accompanied by legal liability related to negligence and possible negligence.Conclusion: Due to the close cooperation of European countries in the form of the European Parliament, important legal issues have been raised and resolved in the form of French and European Union laws and regulations in medicine and health care, including; Confidentiality of electronic health files, considering the nature of these types of files and the possible access of various people to it, the area of authorized activity of specialists and the issuance of licenses, the jurisdiction dealing with possible violations, liability for negligence and errors and technical defects of telemedicine equipment. is, which has been legislated in all subjects according to the needs and conditions of the day.
Pharmaceutical and Cosmetic System Law
Shahriar eslamitabar
Volume 2, Issue 2 , February 2025, , Pages 157-173
Abstract
Background and Objective: economic access to medicine and treatment is one of the most important dimensions of the right to health, which is considered one of the goals of national development in addition to international human rights. Achieving this important goal is possible by using correct and specific ...
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Background and Objective: economic access to medicine and treatment is one of the most important dimensions of the right to health, which is considered one of the goals of national development in addition to international human rights. Achieving this important goal is possible by using correct and specific strategies such as pricing and compensation of costs through insurance.Methods: First, the literature of the article was reviewed using e-books, and articles, then the qualitative data was analyzed through content analysis and a practical model was presented.Results: Price control is done in two ways, direct and indirect. Determining the price and correcting it, it is the direct type, and compensation of costs through insurance is considered the indirect type. As the first control step, pricing strategies are followed based on two basic principles: 1- Value-based pricing, which is related to drug effects and drug cost, and includes the same requirements. 2- Price Classification based on the type and nature of the drug, including generic, under patent and imported.Conclusion: Since Iran has recently abandoned the Cost Plus method (determining the prices based on a percentage more than the total cost), it is necessary to constantly regulated the prices according to the current conditions, needs and the existence of similar drugs, but This action dose not seems correct in any situation and the necessary considerations regarding single-prescription drugs have not been taken into account. While advanced countries such as France and England include all drugs in the insurance coverage list based on their medicinal nature without special requirements and prerequisites, the budget of countries such as Iran does not allow such a thing.
Economic Law and, Financial Health
Shahriar eslamitabar
Volume 1, Issue 1 , June 2024, , Pages 1-9
Abstract
Background: This study seeks to utilize both national and international experiences and explores evolution of health law as an emerging academic field. The right to health is one of the components of human rights, the realization of which is considered necessary for the fulfilment of other human rights ...
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Background: This study seeks to utilize both national and international experiences and explores evolution of health law as an emerging academic field. The right to health is one of the components of human rights, the realization of which is considered necessary for the fulfilment of other human rights and intricately linked to the right to life and is also associated with the right social security. Considering the complexity and development of the relationship between health and law at the national and international levels, it is crucial to reassess this long-established area of law, which has developed into a distinct academic discipline. Health rights can be approached from different perspectives: bioethics, public health rights and health care rights. The first is related to ethics, and the second and third are legal approaches. A central theme in these legal approaches is the the right of individuals to shape their own destinies and to archive a state of health. Methods: Prepared by reviewing articles and guidelines related to health law. Conclusion: Health rights are linked to the rights of individual especially those in vulnerable situations, allowing them access to all aspects of health. Therefore, legal responsibility is a significant aspect of health rights. Morevere, national and international laws require government institutions to take on legal responsibilities for providing, protecting and promoting health. These matters include issues of health care rights, including privacy and confidentiality, legal responsibility of health care professionals, fraud and financial abuse, as well as food and drug rights, environmental rights, mental health rights, and the health rights of vulnerable populations.
