Rajdeep Bioethics
Rajdeep Bioethics
Rajdeep Bioethics
6 3
Council of Europe Declaration of the
Convention Rights of the Child
5 4
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
02
Human 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
03
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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