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Michael Fuchs National ethics councils - Deutscher Ethikrat

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<strong>Michael</strong> <strong>Fuchs</strong> <strong>National</strong> <strong>ethics</strong> <strong>councils</strong>. Their backgrounds, functions and modes of operation compared<br />

and secondary school pupils. Local <strong>ethics</strong> commissions in France have the right to<br />

draw the attention of the national committee to new problems. This sometimes results<br />

in suggestions for reports and Opinions. The provisions of the decree were given<br />

statutory force by the two “Bio<strong>ethics</strong> Laws” of 1994.<br />

Composition<br />

The founding decree provided for a membership of 37. This number was increased<br />

in 1997, so that, in addition to the Chair and two honorary chairs, the Committee<br />

now has 39 members. The Chair is appointed by decree of the President of the Republic.<br />

Another five members belonging to the five principal faiths and philosophies<br />

(Roman Catholicism, Protestantism, Judaism, Islam and Marxism) are also Presidential<br />

appointments. Then come a group of 19 individuals qualified by their competence<br />

and interest in ethical problems, and 15 persons from the research sector.<br />

Those 19 (formerly 16) members are selected by the relevant ministries and the<br />

Prime Minister or appointed from among the members of the <strong>National</strong> Assembly<br />

and the Senate, the Conseil d’Etat and the Court of Cassation by the presidents of<br />

these bodies. As a result two of the Committee’s 42 members are politicians in the<br />

strict sense of the word. The 15 persons from the world of science are members of the<br />

Academies and the major national collèges, research institutes and universities, or are<br />

appointed by them. These statutory requirements have not led to the formation of<br />

blocs. The competence for appointments is not divided among different scientific<br />

cultures or based on a dichotomy between experts and lay persons.<br />

Issues<br />

The formation of the CCNE introduced a form of political advisory activity in<br />

France that had previously been quite unusual (see Byk/Mémeteau 1996). The<br />

founding decree had raised questions of demarcation in relation to the functions of<br />

existing institutions. President Mitterrand’s emphasis on the implications of research<br />

and of novel medical techniques resulted in an attempt to leave the treatment of traditional<br />

issues of medical and professional <strong>ethics</strong> within the field of competence of<br />

the doctors’ professional organizations. However, such a division between matters of<br />

bio<strong>ethics</strong> and research <strong>ethics</strong> on the one hand and professional medical <strong>ethics</strong> on the<br />

other can by no means be regarded as beyond dispute. Furthermore, the CCNE’s repeated<br />

consideration of euthanasia shows how changes in medical technology also<br />

have repercussions on long-established questions of medical <strong>ethics</strong>.<br />

Overall, the tasking of the individual bodies has proved to be a complex process<br />

involving the founding decree and its interpretation, referrals by the competent institutions<br />

of state, the CCNE’s conception of its own role as it has emerged from its<br />

work, and additional legal instruments. Chief among these instruments is the Law on<br />

the Protection of Human Subjects of Medical Research, the Loi Huriet of 1988, which<br />

14<br />

deals comprehensively – that is to say, with a wider field of application than the German<br />

Medicinal Products and Medical Devices Laws – with the functions and status<br />

of <strong>ethics</strong> commissions in such research projects. In addition, this Law put an end to<br />

the debate on whether the existing CCNE ought also to serve as a central commission<br />

for research projects involving human subjects, either as a body to which appeals<br />

could be directed or in order to rule on particularly important or complex cases. The<br />

decision that the regional commissions have sole responsibility for these matters<br />

means that the CCNE must concentrate on general issues. Consideration of the<br />

Opinions hitherto published, however, reveals a broad spectrum, from the very first<br />

Avis, on the sampling of dead human embryonic and fetal tissue, to the eightieth, on<br />

the role of occupational medicine. It extends from the major international issues<br />

such as embryo research or cloning, via psychological research and oncological studies,<br />

to the ethical aspects of neurosurgery, which have hitherto not, or not systematically,<br />

been addressed in bio<strong>ethics</strong>, let alone by advisory bodies.<br />

Mode of Operation<br />

The Committee appoints rapporteurs for the subject-matter under consideration,<br />

who are responsible for the scientific question, the research problem or the ethical issue<br />

concerned. A working party made up of members of the Committee and external<br />

specialists is formed, and begins by determining whether the issue in hand is a<br />

genuine scientific problem and whether it has not already been examined by the<br />

Committee or is not covered by existing law. The working party then approaches the<br />

documentation centre (Centre de Documentation en Ethique) of the INSERM (Institut<br />

<strong>National</strong> de la Santé et de la Recherche Médicale); the founding decree provides<br />

that the CCNE shall receive administrative and technical support from this body. In<br />

particular, the INSERM is required to provide the Ethics Committee with a documentation<br />

and information centre on the <strong>ethics</strong> of the life and health sciences. Next<br />

comes the ethical debate, which may extend over several months. Its outcome is a scientific<br />

report, an ethical report and a draft Opinion (Avis) which are published and<br />

forwarded to the Committee’s Technical Department and to a 14-member subcommittee.<br />

The latter submits the text, after examination and discussion, to the Plenary<br />

Committee, which meets at approximately six-weekly intervals to consider and discuss<br />

the drafts. It then returns the text to the working party for revision. In most cases,<br />

the Committee finally adopts the report together with the Opinion unanimously.<br />

However, dissenting positions are allowed for and have in some cases been expressed,<br />

attached to the report and published with it. In some cases, areas of consensus and<br />

dissent are recorded, but not the results of a vote on dissenting positions.<br />

In addition to the working parties assembled for the purpose of compiling an<br />

Avis, there is a permanent working group on molecular biology and reproductive<br />

techniques and another on the neurosciences.<br />

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