Professional Documents
Culture Documents
Rajdeep Bioethics
Rajdeep Bioethics
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Council of Europe Declaration of the
Convention Rights of the Child
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International Code of Geneva Decleration
Medical Ethics
INTRODUCTION
The first international documents on medical ethics and bioethics were produced in the aftermath of the Second World War and,
therefore, focused on biomedical research with human subjects. In the following decades different institutions dedicated to
bioethics were created, some of them in the international realm, such as the Council for International Organizations of Medical
Sciences, the Council of Europe, WHO, and UNESCO – these last three, having a larger scope, established specialized
departments and/or programs on bioethics.
There are a growing number of international documents on medical ethics and bioethics. They started to be produced after the
Second World War, and they still keep their original and common goal to establish a core of ethical principles aiming to
standardize the rules of action in the widest scope possible.
The majority of these international documents are nonlegislative; they are of an ethical and deontological nature and not legally
binding. Nevertheless, their influence at the regulatory and political levels is very significant, also depending on the nature and
political representativeness of the institution or body that issues the document, as well as on the level of consensus reached and
the legal nature of the document itself.
01 Nuremberg Code
Among these first international documents, the most important is the Nuremberg Code, in 1947. It is
committed to establish the ethical requirements for biomedical research involving human subjects.
The Nuremberg Code is a ten-point statement of the final judgment of the Nazi doctor’s trial and has
become part of international law, still prevailing at the basis of all documents concerning the ethics of
research with human subjects.
As a consequence of the trial of physicians (the Doctors’ Trial) who had conducted atrocious
experiments on unconsenting prisoners and detainees during the second world war. The Code, designed
to protect the integrity of the research subject, set out conditions for the ethical conduct of research
involving human subjects, emphasizing their voluntary consent to research.
Universal Declaration of Human
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Rights
The Universal Declaration of Human Rights was adopted by the General Assembly of the United
Nations in 1948.
The Universal Declaration of Bioethics and Human Rights is the only international document that
intends to put together the most fundamental bioethical principles to be applied to biomedical research,
clinical practice, healthcare policies, and to international cooperation at the three men- tioned levels.
Article 7 of the Covenant states "No one shall be subjected to torture or to cruel, inhuman or degrading
treatment or punishment. In particular, no one shall be subjected without his free consent to medical or
scientific experimentation". It is through this statement that society expresses the fundamental human
value that is held to govern all research involving human subjects – the protection of the rights and
welfare of all human subjects of scientific experimentation.
Declaration of the
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Rights of the Child
It draws on the principles established by the European Convention on Human Rights, in the field of biology and medicine.
It is a framework Convention aiming at protecting the dignity and identity of all human beings and guarantee everyone,
without discrimination, respect for their integrity and other rights and fundamental freedoms with regard to the application
of biology and medicine.
It sets out fundamental principles applicable to daily medical practice and is regarded as such at the European treaty on
patient’s rights. It also deals specifically with biomedical research, genetics and transplantation of organ and tissues.
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