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.
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.
Religious and Spiritual Rights in Health
Asghar Arabian; Mohammadreza Alipour; Maryam Haidari
Volume 2, Issue 2 , February 2025, , Pages 17-30
Abstract
Background and Objective: Health is known as one of the main pillars of development and one of human rights. Therefore, governments are obliged to realize the right to health of their citizens. Judicial and quasi-judicial mechanisms sieve as important avenves for individual to pursue this right, and ...
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Background and Objective: Health is known as one of the main pillars of development and one of human rights. Therefore, governments are obliged to realize the right to health of their citizens. Judicial and quasi-judicial mechanisms sieve as important avenves for individual to pursue this right, and their incorporation into legal framework is essential. The involvement of experts in health and criminal sciences.Methods: With scientific methods, the analysis and recognition of the right to health in national and international law has been done and provide practical solutions to help improve the monitoring and handling of the violation of the right to health in Iran.Results: Based on international documents, all the governments are committed to the health rights of their citizens. Therefore, the governments put cases of violations of this right under judicial review at two levels: Violation of the right to health by 1- Healthcare professionals, 2- The government; Therefore, both of them are responsibl.Conclusion: Success in judicial and quasi-judicial processes depends on the implementation of international obligations related to the right to health by governments. The right to health should be the first priority of the laws of the countries; And among other things, it should be accurately and clearly considered in the constitution, and it should be linked with the more fundamental right to life. However, achiving this right presents significant challenges, such as broad scope of health rights, the need for clear definitions of their limits, insufficient expertise among profesionals involved, inadequate judicial evaluations, and funding limitations.
Mental Health Law and Behavioral Sciences
Roza Haghgoo; Sima Rasouli
Volume 1, Issue 1 , June 2024, , Pages 17-30
Abstract
Background and Objective: Heallth care professions have a special place in society in terms of building trust. In order to maintain trust and proper communication with patients, these professions are committed to complying with ethical standards at the highest level, which is actually the basis of a ...
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Background and Objective: Heallth care professions have a special place in society in terms of building trust. In order to maintain trust and proper communication with patients, these professions are committed to complying with ethical standards at the highest level, which is actually the basis of a successful relationship between these professionals and patients, that lead to gain trust and maintaining their peace of mind.Methods: First, two questionnaires were completed by dentists and patients; and then, the data was analyzed by SPSS software and descriptive statistics.Results: This research, which was conducted with the participation of 39 dentists and 260 patients and using questionnaires and special SPSS software to evaluate the level of trust of patients in dentists and the level of communication skills applied by dentists, showed that many patients trusted the recommendations Medicine of dentists and did not look for the second theory. In this cases, most patients were sure of the confidentiality of their personal medical information.Conclusion: Based on the results of the present study, the communication skills of the dentists of Shahid Mohammad Montazeri Clinic, in both verbal and non-verbal dimensions, are acceptable to the patients.
Healthcare Law
arash abdi; Yaser Zandishafag; salar zeynali
Volume 1, Issue 1 , June 2024, , Pages 11-22
Abstract
Background and Objective: The advancement of science and technology in the field of electronic communications has caused huge changes in the scientific, practical and applied fields, including educational and therapeutic services. Smart medical universities and smart hospitals are one of these important ...
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Background and Objective: The advancement of science and technology in the field of electronic communications has caused huge changes in the scientific, practical and applied fields, including educational and therapeutic services. Smart medical universities and smart hospitals are one of these important developments. Each of these new ideas has its own advantages and disadvantages.Methods: First, the literature of the article was reviewed using e-books, and articles, then the qualitative data was analyzed through content analysis and an applied theory titled the “Integrated Digital-Human Health” was presented.Results: Reduction of training costs, no need for a training place, the possibility of using multimedia tools, flexibility in the time and method of training, facilitating the storage of materials, reducing the time and cost of travel, and speeding up interactive processes are known among the advantages of virtual training. More access to services, better selection of centers and doctors, ease of hospitalization and use of services, remote control of patient condition and better support of service recipients are considered to be the advantages of virtual hospitals.Conclusion: Due to the difficulty and sensitivity of some concepts and the practicality of some medical courses, it is not possible to teach in this field only through virtual means. Therefore, combined training consisting of face-to-face and virtual classes is recommended. The field of medical sciences, which is a human-oriented field with an emphasis on the relationship between doctors and paramedics and patients, should not be satisfied only with the virtual relationship that strengthens the sense of isolation
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.
The right to health and bioethics
Ansieh Zarenejad; Fatemeh Anvar; Maryam Haji
Volume 1, Issue 1 , June 2024, , Pages 37-52
Abstract
Background and Objective: Since the beginning of the 1990s, economic sanctions have been increasingly used by major powers in the western block in order to achieve international political goals. Over the years, economic sanctions have caused violations of the right to health in the targeted countries.Methods: ...
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Background and Objective: Since the beginning of the 1990s, economic sanctions have been increasingly used by major powers in the western block in order to achieve international political goals. Over the years, economic sanctions have caused violations of the right to health in the targeted countries.Methods: In this article, the impact of sanctions on Iran and other countries is compared and solutions are suggested to reduce the negative effects of sanctions on Iran's economy and health. Also, the best model for dealing with sanctions for Iran's health system was presented.Results: The imposed sanctions are purely economic and based on putting pressure on the governments, but what happened in reality is the violation of the principles of human rights in the countries under sanctions. The severity of these anti-human rights effects is closely related, especially with the duration of sanctions, as well as with the economic foundation of the target country.Conclusion: Iran is not the first country to be sanctioned; Therefore, the adverse effects of sanctions on the people of this country were predictable by the Security Council and the countries that imposed the sanctions. In the future, before applying any economic sanctions, the international community must take effective measures to protect the human rights of the people of the target country. Also, use any political and legal means to prevent the violation of the rights of these people by other countries or international organizations.
Economic Law and, Financial Health
Seyyed Babak Mozafari; Mahdi Saeedian; Shirin Khalili
Volume 2, Issue 2 , February 2025, , Pages 43-55
Abstract
Background and Objective: Considering the complexity and development of the relationship between health care professionals and patients on the internet at the national and international levels, it is necessary for us to know of this new technology.Methods: This article has been written using the books ...
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Background and Objective: Considering the complexity and development of the relationship between health care professionals and patients on the internet at the national and international levels, it is necessary for us to know of this new technology.Methods: This article has been written using the books and articles available in real and virtual libraries in a descriptive-explanatory way.Results: The ever-increasing growth of the communication, telecommunication and informatics industries confronts the world with a new revolution every day. The revolution of information and communication technology has left a significant impact on all economic, social, political and security sectors of the countries. With the development of this technology in the medical sector, we are looking for a huge transformation in the system of providing health and medical services, and one of the most important areas of application of information technology is the field of health and treatment.Conclusion: Electronic health refers to the use of the internet and other technologies in the health care industry. Electronic health is a combination of informatics, health and business disciplines and refers to health information and services that are provided through the Internet and digital technologies. In this system, healthcare service providers and patients are not in face-to-face contact, and the communication between them is done by electronic devices, for example by computer.
Law and Forensic Medicine
Abdul Hassan Kazemi; Ali Eslamifar; Mohsen Saberi Isfeedvajani
Volume 1, Issue 1 , June 2024, , Pages 53-69
Abstract
Background and Objective: One of the stages of approval a drug or treatment method as a standard product or method in legal centers is clinical trial involving human samples. Since the efficacy of the tested drugs and treatments have not been proven yet, individual participating in these trials face ...
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Background and Objective: One of the stages of approval a drug or treatment method as a standard product or method in legal centers is clinical trial involving human samples. Since the efficacy of the tested drugs and treatments have not been proven yet, individual participating in these trials face inherent risks. therefore, ethics and law demand the protection for these people and the prevention of risks and the compensation for damages resulting from adverse events.Methods: In this article, the ethical and legal issues of therapeutic and non-therapeutic clinical trials are investigated and the model of the best method for conducting clinical trials from an ethical perspective is presented.Results: Biomedical researches are conducted in different methods and clinical trials on human samples face the most ethical and legal issues and challenges. Among the most important challenges are unacceptable risks to the participants, obtaining informed consent, especially for individuals without mental capacity and children, negligence and negligence of researchers and compensation for possible damages to the participants.Conclusion: By modeling to the regulations related to clinical trials on human samples in EU member countries, including England, not only the right to freedom and individual independence of humans is respected; Rather, the lives and health of the participants are also safegaurded. This dual focus is also emphasized in Islamic jurisprudence. The legal issues of the use of specific populations such as prisoners, children, patients and cognitively impaired adults has not escaped the attention of legislators in leading countries.
Law Policy Management,, and Regulation of Health
mehdi sanei; salar shahbazi; Najibeh Mirani
Volume 2, Issue 2 , February 2025, , Pages 57-66
Abstract
Background and purpose: Considering the advantages of biological weapons, such as cheap production, easier use, high efficiency, very high emission power, dual purpose use and the ability to hide the idea of illegal activity, we see a significant increase in the production, development and possibility ...
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Background and purpose: Considering the advantages of biological weapons, such as cheap production, easier use, high efficiency, very high emission power, dual purpose use and the ability to hide the idea of illegal activity, we see a significant increase in the production, development and possibility of using these deadly weapons. Therefore, it is necessary to deal seriously with the phenomenon of bioterrorism, especially through legislative measures.Method: This article has been written using the paper and e-books and articles in a descriptive-explanatory method.Findings: "Bioterrorism" means: the deliberate release or release of viruses, bacteria and other pathogenic agents, with the intention of causing disease or death among human, animal and plant populations.Since bioterrorism is considered a global threat, important international treaties such as the Geneva Protocol and the Convention on the Prohibition of the Development of Biological Weapons have been signed by most of the governments, but the problems and deficiencies in the text of these treaties and the lack of necessary enforcement guarantees cause It has provided for repeated violations of the provisions of these treaties. The implementation problems related to the way of inspections and the biased and discriminatory approach of some countries have also become the reason for the fact that today more than in the past, we are witnessing deadly bioterrorist attacks in every corner of the world.Conclusion: Currently, countries such as the United States, which are highly exposed to bioterrorism attacks, have developed and passed national laws to deal with the sinister phenomenon of bioterrorism, and this is while the Islamic Republic of Iran only The microbial comprehensive plan, which is a general plan, is enough and has not taken any urgent action to protect public health from the scourge of this ominous phenomenon.
Food and Agricultural Industry Law
Rahim RahbarNouhi; Mohammad Reza Dehghani
Volume 2, Issue 2 , February 2025, , Pages 67-85
Abstract
Background and Objective: Marinol is actually the first cannabinoid drug approved by the US FDA in 1985. The approved use of this drug in reducing the side effects caused by chemotherapy of cancer patients such as anorexia, nausea, pain and vomiting, as well as its use in the treatment of weight loss ...
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Background and Objective: Marinol is actually the first cannabinoid drug approved by the US FDA in 1985. The approved use of this drug in reducing the side effects caused by chemotherapy of cancer patients such as anorexia, nausea, pain and vomiting, as well as its use in the treatment of weight loss in AIDS patients has also been approved in 1992.Methods: In this article, while referring to a summary of the history of medicinal cannabis, we review Marinol. Also, investigation and understanding of how herbal cannabinoids helps the endocannabinoid system, which is responsible for the health balance (Homeostasis) of the body, has been taken into consideration. In this work, the necessary operations have been carried out, from seed germination to the preparation of medicine (vegetable Marinol) and the preparation of capsules. Monitoring and analysis of cannabinoids was done by a gas chromatography device connected to a mass spectrometer (GC/Mass Spectroscopy).Results: The efficiency of the resin in the flower was 38%, which was obtained at the optimum point of 97.5% of THC and 2.5% of cannabinoids, and the main part was cannabinol, and thus the percentage of the effective substance in the plant was 37.05%. After dissolving the solvent at room temperature, we will dissolve the obtained resin in sesame oil and in this way, we will be able to encapsulate different doses of vegetable Marinol.Conclusion: The idea of using plant Marinol (cannabis flower extract (resin)) with high THC in pure sesame oil instead of synthetic dronabinol (chemical cannabinol) can be derived from less side effects, higher therapeutic effect, less persistence in the body and cheaper price. It is related to the chemical type of this drug.
Healthcare Law
Bahram Mofid; Mehdi Dostdary; Abbas Karimi Mojarad
Volume 1, Issue 1 , June 2024, , Pages 71-82
Abstract
Background and Objective: Industrial living conditions, the increase in the population of elderly people and the occurrence of chronic and incurable diseases have caused patients to use drugs and complementary and alternative medicine methods, including methods based on biofield or aura. These methods ...
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Background and Objective: Industrial living conditions, the increase in the population of elderly people and the occurrence of chronic and incurable diseases have caused patients to use drugs and complementary and alternative medicine methods, including methods based on biofield or aura. These methods do not have the risks of side effects of chemical drugs and the high cost of common modern medical treatments. In order to be used optimally, this ancient medicine needs legal control and supervision in order to prevent financial abuse and fraud, as well as the negligence of therapists.Methods: Regulatory methods and laws for complementary and alternative medicine in the world have been reviewed and the best regulatory methods and laws for it in Iran have been presented.Results: Every medical field requires legislation, legal control supervision, and even inspection. In addition to ensuring quality, efficiency, and reducing the risk of using tools and methods, such measures help prevent abuse and fraud. This issue is particularly significant in the field of complementary medicine, where there is a great need for a relationship based on trust between the therapist and the patient.Conclusion: Due to the high risk of financial abuse and fraud, it is necessary to develop and enforce the necessary regulations to address false claims and fraud in the use of complementary and alternative medicine methods. Educational standards should also be carefully applied in this field to prevent the employment of uninformed and unqualified people in this field, because the activity of these people causes damage to people's trust.
Law Policy Management,, and Regulation of Health
Abbas Vosoogh-Moghaddam; Seyed Sahand Eisapoor; Hassan Kakui
Volume 1, Issue 1 , June 2024, , Pages 83-98
Abstract
Background and Objective: In order to follow international policies related to the realization of the four dimension of human rights, including the right to health, governments have three obligations, commitment to respect, commitment to support, and commitment to implementation. Governments must take ...
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Background and Objective: In order to follow international policies related to the realization of the four dimension of human rights, including the right to health, governments have three obligations, commitment to respect, commitment to support, and commitment to implementation. Governments must take certain action that one of them is to evaluate the extent of realization in various dimensions of human rights, especialy the right to health.Methods: This article has been written using paper and e-books as well as articles employing a descriptive-annotative method.Results: generally, evaluation indicators are divided into two main types: general and specific indicators. In addition, each indicator must possess the characteristics of being transparent, accurate, comprehensive, valid and acceptable, and related to the subject being evaluated.Conclusion: There are serious concerns regarding the evaluation of quality indicators, including the collection of information, alignment of data from different sources and integration of these data. Additionally, the overlap and interference of indicators in som areas related to evaluation of the right to health contribute to lack of information. The national health indicators used in the Islamic Republic of Iran appear to have flaws. By comparing domestic and international indicators, it may be possible to develop a composite index, that integrates links different dimensions and approaches.ش
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
Abbas Kebriaeezadeh; Vahideh Montazeri Najafabadi; Roya Ayazi-Nasrabadi
Volume 1, Issue 1 , June 2024, , Pages 99-113
Abstract
Background and Objective: According to the right to health, one of the most basic human rights, all individual have the right to essential medicines. These medicines should be available to those in need at the appropriate time and at a reasonable cost.Methods: This article has been written using both ...
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Background and Objective: According to the right to health, one of the most basic human rights, all individual have the right to essential medicines. These medicines should be available to those in need at the appropriate time and at a reasonable cost.Methods: This article has been written using both printed books and e-books, as well as articles and documents, and employes a comparative-analytical for examination.Results: From the perspective of the World Health Organization, access to essential medicines, regard asfunamental right and key indicator of the right to health. This issue is particulary significant for som countries, especially that are poor and less developed, due to concern about affordability. Because of the vital importance of these medicine, the World Health Organization publishes a list of essential medicine every two years, according to based on minimum needs.Conclusion: Although the Islamic Republic of Iran has taken serious measures to address the pharmaceutical needs of its citizens by regulating price and the drug market, especially through the import of drugs and the implementation of the generic plan, serious work has not been done regarding the preparation of the list of essential medicines. However, considering the rejection of this need and reaching the relative self-sufficiency in the country, through the comprehensive generic plan, adjusting the internal list according to the World Health Organization’s list does not seem necessary. Each country has its own independent list of essential medicines based on its production capacity and needs.
Economic Law and, Financial Health
seyyed mohammad ali mirbehbehani; morteza meftahi
Volume 2, Issue 2 , February 2025, , Pages 107-118
Abstract
Background and purpose: Perhaps the most important part of health is medicine. A access to Pharmaceutical Products is considered one of the pillars of human rights. This directly affects the right to health and the right to life. Considering that high-cost and highly effective pharmaceutical products ...
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Background and purpose: Perhaps the most important part of health is medicine. A access to Pharmaceutical Products is considered one of the pillars of human rights. This directly affects the right to health and the right to life. Considering that high-cost and highly effective pharmaceutical products account for a huge share of household expenses, in order to ensure relative justice in access, appropriate price determination and optimal price control methods are required.Research Method: This article has been written using the paper and e-books and articles available in real and virtual libraries in descriptive-explanatory method.Findings: Determining the price ceiling is the first step in controlling the price of pharmaceutical products, which is determined based on considerations such as cost, benefits, risks of using drugs, or market conditions. Sometimes governments do not consider any of these requirements in order to follow the free market policy. According to the nature of drugs, these controls are carried out in three categories: brand, generic and imported drugs, although some drugs may be included in the combined category. Due to the high cost and the importance of innovation, price control of brand products is more important and complicated.Conclusion: Determining the price ceiling and fighting against overselling in order to support production and innovation with the aim of supporting the consumer are necessary as ways to determine and control drug prices. For this purpose, the fight against price gouging regarding imported products is done in support of domestic production. Compulsory licensing is also another good way to control the price of branded pharmaceutical products.
Environmental Law and Occupational Health
Jalil Maleki; Ehsan Lame; Farzad chghamirza; Najibeh Mirani
Volume 1, Issue 1 , June 2024, , Pages 115-129
Abstract
Background and Objective: Preserving the enviroment is essential for human life, and this required preventing pollution, misuse and exploitation. The purpose of this article is to review the framework of the legal system and the status of the statuse of global regulations related to environmental rights, ...
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Background and Objective: Preserving the enviroment is essential for human life, and this required preventing pollution, misuse and exploitation. The purpose of this article is to review the framework of the legal system and the status of the statuse of global regulations related to environmental rights, with a focuse on the measures and requirements related to commercial and market activities. The aim is to analyze these issues within developing countries and provide insights for those in the early stages of creating and implementing such regulations.Methods: This article was written using a combination of printed materials, e-books and academic articles, employing a descriptive-explanatory approach.Results: In today's world, the environmental preservation has been effectively pursued in some countries through the establishment of laws and regulations. Key sources for legal protection and preservation of the environment include international laws and treaties, constitutional guidelines, laws approved by the European Union Parliament, regulations of regulatory organizations, and court rulings.Conclusion: Legislators should pursue sustainable development by predicting and impose taxes on environmental polluters, not extending or revoking licenses for destructive industries, establish and enforce regulations related to environmental protection responsibility. Additionally, incentive measures such as exemption for those who contribute to a clean environment could be effective. Environmental insurance, as a policy adopted by the European Union, is also for security of industries at risk at environmental pollution.
Environmental Law and Occupational Health
Ali Darvishi Boloorani; Yaser Zandi Shafagh
Volume 2, Issue 2 , February 2025, , Pages 119-135
Abstract
Background and Objective: The entanglement and link between the environment and human health is very deep and complex, therefore, increasing awareness and comprehensive investigation is required. Pursuing a preventive approach over a reactive approach can prevent the occurrence of many environmental ...
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Background and Objective: The entanglement and link between the environment and human health is very deep and complex, therefore, increasing awareness and comprehensive investigation is required. Pursuing a preventive approach over a reactive approach can prevent the occurrence of many environmental and health problems, if they occur, reduce the consequences to a minimum.Methods: This article has been prepared in a descriptive-explanatory method, using thee paper and e-books and articles and document.Results: The destructive effects of human activities on the environment and the subsequent feedback of those consequences, especially in the field of health, which has plagued mankind, are known in most cases and even predictions have been made for them. Now it is necessary to determine what works and activities humans should do that not only do not have destructive and bad effects on the environment, but can also reduce the negative effects of the past destructive activities and in the shadow of intractive activities, human health can be provided and preserved as much as possible.Conclusion: In this article, due to maintaining the integrity of the content and achieving the result, only three main factors that have a direct cause and effect relationship between human activities and its impact on the environment are considered in the presented model. However, due to the existential nature of humans and the environment, which are both living and dynamic beings, it is not possible to consider only a linear and direct relationship.
Law and Forensic Medicine
Mohammad Reza Elahimanesh; Javad Alizadeh
Volume 1, Issue 1 , June 2024, , Pages 131-146
Abstract
Background and Objective: "Euthanasia" is one of the most controversial issues "Bioethics" and a sibnificant topic in health law, with various ethical, legal and jurisprudential aspect to be studied. Since the teachings and sources of Islamic jurisprudence form the foundation of our country's, strengthening ...
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Background and Objective: "Euthanasia" is one of the most controversial issues "Bioethics" and a sibnificant topic in health law, with various ethical, legal and jurisprudential aspect to be studied. Since the teachings and sources of Islamic jurisprudence form the foundation of our country's, strengthening the jurisprudential aspect can legal structure.Methods: In this article, a comprehensive definition of euthanasia is provided. Along with an exploration of its types and an overview of prominent Shia jurists viewpoints, wich are considered significant in their own right. Additionally, relevant verses and traditions are utilized to interpret and justify the aforementioned rulings.Results: In Iran, the legal vacuum regarding euthanasia is quite noticeable, since Shia jurisprudence forms the basis of the legal structure of our country, it is essential for jurists, and respected legislators. To address this legal gap and establish comprehensive laws that clearly address euthanasia and its various aspects, it’s necessary to develop and implement such legislation.Conclusion: Examining euthanasia from the perspective mandatory ruling (permissibility or non-permissibility) and its status ruling (right to retribution and dowry), is one of the topics of interest in this article. The examination is accompanied by jurisprudential and philosophical justification and interpretation. In addition, Article 206 of the Islamic Penal Code has also been carefully examined in this regard. Finally, by presenting the views of Shiite scholars on various aspects of euthanasia, a general summary is provided, which is hoped to clarify the issue and elucidate the jurisprudence and laws, considering the current conditions.
Law Policy Management,, and Regulation of Health
Mehdi Moazzami goudarzi; seyed sahand eisapoor
Volume 2, Issue 2 , February 2025, , Pages 137-156
Abstract
Background and Objective: To ensure safety, now a day, cosmetic products as a part of prerequisites for health services has been regulated worldwide. Methods: This study has been designed based on comparison between main regulations within some huge markets of manufacturing and consumption of cosmetics ...
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Background and Objective: To ensure safety, now a day, cosmetic products as a part of prerequisites for health services has been regulated worldwide. Methods: This study has been designed based on comparison between main regulations within some huge markets of manufacturing and consumption of cosmetics around the world. Then the comparison has been analyzed. Results: On the other hand, however the basis of authorities’ systems to regulate cosmetics are fundamentally same and follow some equal scientific lines, by the way there are some Meaningful differences in case of product definition and grouping.Conclusion: Lack of consensus in cosmetic regulation now a day easily affected innovation, research and development and international cosmetic trading. Unity of international procedures in regulation at the same time prepares ensure for products safety and facilitate for progressive innovation, research and development, competition and international trading.
New Technologies Health and Law
Babak Sabet; Mahdi Saidian; Shirin Khalili
Volume 1, Issue 1 , June 2024, , Pages 147-162
Abstract
Background and Objective: Today, with the extensive progress of information technology, its role in the health sector has become more important than ever before. However, these applications create new challenges for privacy. As a result, governments are trying to take various measures, including passing ...
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Background and Objective: Today, with the extensive progress of information technology, its role in the health sector has become more important than ever before. However, these applications create new challenges for privacy. As a result, governments are trying to take various measures, including passing criminal legislation, to address these challenges.Methods: In this article, by comparing the criminal requirements of electronic health files in leading countries and Iran, by presenting a strategic model in this regard, suggestions have been made to improve the security and confidentiality of electronic health files.Results: This comparative article examines electronic health records with a particular focuse on confidentiality in Europe, America and Iran from a criminal law perspective. Due a absence of comprehensive law specifically addressing "electronic health" and judicial procedures in Iran, related legislation such as the Islamic Penal Code, the Electronic Commerce Law, the Computer Crimes Law and the laws supporting the comprehensive health information system are addressed.Conclusion: Different countries adopt various approaches to the protection of personal health data. European Union countries on individual rights and freedoms. In contrast, the United States is seeking to implement tougher penalties to is looking for the approval of tougher punishments to deal with such crimes. Iran is working to establish legal protection for privacy and personal information through a ten-year program, utilizing legislative model from leading conteies with comidering Islamic Jurisprudence and cultural contexts. Considering the extensive and rapid growth of the field of electronic health, it is necessary to adopt a specialized legislative approach for this area.
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.
New Technologies Health and Law
Maryam Bahrkazemi; Amireza Mahmudi
Volume 1, Issue 1 , June 2024, , Pages 163-177
Abstract
Background and Objective: According to the ever-increasing advances in the field of artificial intelligence, this technology can have positive and negative effects on health rights and healthcare. Artificial intelligence may create challenges and gaps in the field of violation of patients' privacy, violation ...
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Background and Objective: According to the ever-increasing advances in the field of artificial intelligence, this technology can have positive and negative effects on health rights and healthcare. Artificial intelligence may create challenges and gaps in the field of violation of patients' privacy, violation of doctor's credibility, which leads to disregard for human rights and negative effects on the relationship between doctor and patient. One of the most important goals of research on the impact of artificial intelligence on healthcare services is to identify the strengths and weaknesses of healthcare systems based on artificial intelligence.Methods: This is a theoretical research with analytical-descriptive research method which is the method of collecting information in library form.Results: In this research, we will identify and analyze the challenges in the use of artificial intelligence in the field of health, and also provide appropriate solutions to protect human rights and improve health and treatment services, and better understand the effects of artificial intelligence on the efficiency of health systems and We provide treatment.Conclusion: This technology can significantly improve the accuracy of disease diagnosis, increase access to health services and improve the quality of medical care. But at the same time, there are also ethical, legal, and privacy concerns that need to be properly investigated and carried out using artificial intelligence in the field of health.
Healthcare Law
Mehdi Doostdari; Fatemeh Anvar
Volume 2, Issue 2 , February 2025, , Pages 175-187
Abstract
Background and Aims: Considering the necessity of integrating traditional medicine in modern academic medicine, it is necessary to evaluate and carefully consider the opportunities and challenges of complementary and alternative medicine in this integration, so that based on regulations and policy frameworks, ...
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Background and Aims: Considering the necessity of integrating traditional medicine in modern academic medicine, it is necessary to evaluate and carefully consider the opportunities and challenges of complementary and alternative medicine in this integration, so that based on regulations and policy frameworks, Legal, ethical, regulatory, educational and research studies are necessary for each country or geographical area.Material & methods: This article was written using the books and articles available in real and virtual libraries in a descriptive-explanatory way.Results:Integrating complementary medicine with all patie medicine brings many opportunities and at the same time challenges. The most important challenges are legal and ethical challenges, regulation, formulation and implementation of the training program and attention to research-orientedness and validity of research, especially complementary medicine clinical research. Every medical field needs legislation, control and legal supervision from inside or outside the organization. In addition to guaranteeing the quality, efficiency and reducing the risk of using tools and methods, this work prevents any abuse and fraud. This issue is more important in the field of complementary medicine, where there is a great need for a relationship based on trust between the therapist and the patient.Conclusion: Integrating of traditional and complimentary medicine into conventional medicine, despite its many advantages, faces serious challenges that require appropriate stategies in the fields of law making, regulatory and quality control, education and research. In the legal field, it is necessary to have appropriate laws for the purpose of issuing employment licenses and clarifying the quality standards of specialists, including avoiding negligence and mistakes, and compensating for damages through increasing medical liability insurance coverage and ways to avoid legal liability, including acquiring Informed consent and privacy should be included in the rules. Regulation in both product and specialist sectors should be implemented carefully in terms of quality, safety and efficiency of products and methods
Pharmaceutical and Cosmetic System Law
Seyed Mohammad Ali mir Behbahan; morteza meftahi
Articles in Press, Accepted Manuscript, Available Online from 19 January 2025
Abstract
This article examines the state of pharmaceutical regulations in the developing world by constructing international indices derived from World Health Organization data. The past two decades have been marked by profound changes in the pharmaceutical sector, including a complete overhaul of intellectual ...
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This article examines the state of pharmaceutical regulations in the developing world by constructing international indices derived from World Health Organization data. The past two decades have been marked by profound changes in the pharmaceutical sector, including a complete overhaul of intellectual property systems at the behest of the World Trade Organization and the consolidation of global active pharmaceutical ingredient suppliers in China and India. Although drug ownership laws have been regulated and implemented globally, we surprisingly have little information about how national market entry standards and the regulation of pharmaceutical products have changed.
