German Ethics Council


German Ethics Council is an independent council of experts in Germany addressing the questions of ethics, society, science, medicine and law and the probable consequences for the individual and society that result in connection with research and development, in particular in the field of the life sciences and their application to humanity. Its duties include informing the public and encouraging discussion in society, preparing opinions and recommendations for political and legislative action for the Federal Government and the German Bundestag as well as cooperating with national ethics councils and comparable institutions of other states and of international organisations.
The Ethics Council Act, that entered into force on 1 August 2007, forms the basis for its activities.
Half of the 26 members are proposed by the Federal Government, while the other half of the 26 members is proposed by the Bundestag. The members of the German Ethics Council are then designated by the President of the Bundestag for four years. Through this procedure, different ethical approaches and a pluralistic spectrum of opinion should be represented. Independence is to be ensured, amongst others, by prohibiting the members to belong to the Federal Parliament or the Federal Government or to a Federal States’ Parliament or Government respectively.

Tasks

The German Ethics Council fulfils a dual function as a forum for dialogue and an advisory body. In its function as an ethical dialogue forum, the German Ethics Council is intended, in accordance with its legal basis, to bring together specialist scientific discourses and to promote the debate in society, particularly through public events. In its function as a bioethical advisory body, the German Ethics Council has the task of drawing up statements and recommendations for political or legislative action. The Council ensures cooperation with other ethics bodies at national and international level.
The German Ethics Council acts either on its own initiative or mandated by the Federal Government and the German Bundestag. The Council reports once a year to the German Bundestag and the Federal Government on its activities and the state of the debate in society.
In order to inform the public and encourage discussion in society, the Council organises public events and provides information about its activities on its website, in its newsletter and annual report. Besides a series of public evening events called “Bioethics Forum” and its annual meeting – both taking place in Berlin – the Council also organises public events outside of Berlin.

Functioning

Generally, the Council meets once a month; meetings are open to the public. In addition to these plenary sessions, the work on content is mainly carried out in working groups which are formed by decision of the plenary session on specific topics and meet at irregular intervals. The work of the Council is supported by an administrative office, which is located in Berlin at the Berlin-Brandenburg Academy of Sciences and Humanities.
In 2018, the budget of the German Bundestag provided 1.895 million euros for the Council's work.
Once a year, a public annual conference of the German Ethics Council takes place in Berlin; together with external experts, the German Ethics Council advises and discusses in a full-day event on its current topics. Conference topics of the last years were: Care – Robot – Ethics. Ethical Challenges in the Technologisation of Care, Human Dignity in Our Hands – Challenges from New Technologies, Autonomous systems. How intelligent machines are changing us, Access to the human genome. New possibilities and their ethical evaluation, The quantified human – big data and health.
In addition, the Council organizes a series of public evening events in Berlin called Bioethics Forums. These events, usually introduced by guest lectures, aime at publicly discussing concrete biopolitical issues. Topics of the last years were: Advantages and disadvantages of opt-out organ donation, Rare diseases, Egg donation abroad and the consequences of this practice in Germany, Antibiotic resistance, Disease mongering, People with disabilities – a challenge for hospitals.

Members

The German Ethics Council consists of 26 members who shall exercise their office in person and independently. They may not belong either to the Federal Parliament or the Federal Government or to a Federal States’ Parliament or Government respectively. They represent scientific, medical, theological, ethical, social, economic and legal concerns in a particular way and ensure a variety of ethical approaches and a pluralist spectrum of opinions. The members are appointed for a period of four years. A one-time reappointment is possible. If a member resigns prematurely, a new member is appointed for four years.

Members since April 2020

The President of the German Bundestag, Wolfgang Schäuble, has appointed 21 members to the German Ethics Council as of 30 April 2020. Several members had reached the end of their terms with the body on 10 April 2020, among them the previous chairman Peter Dabrock. Including three members who were appointed outside the regular cycle between 2016 and 2018, the German Ethics Council has 24 members since 30 April 2020.
On 11 April 2016, the President of the Bundestag, Norbert Lammert, appointed the following members of the Ethics Council for the first or second time, respectively:
The following scholars, whose appointment period had not yet expired in April 2016, were also members of the German Ethics Council in 2016:
Changes since 2017:
Chair and Vice-Chairs since April 2016
At the constituent meeting of the German Ethics Council on 28 April 2016, Peter Dabrock was elected Chair of the Council, Katrin Amunts, Andreas Kruse and Claudia Wiesemann Vice-Chairs.
Following Andreas Kruse‘s resignation from the Council at the end of April 2018, Council member Volker Lipp was elected Vice-Chair at the plenary meeting on 17 May 2018.

Members 2012–2016

On 11 April 2012, the then President of the Bundestag Norbert Lammert appointed the following members for the German Ethics Council’s second term:
During the constituting assembly, the German Ethics Council elected Christiane Woopen as chairwoman as well as Wolf-Michael Catenhusen, Peter Dabrock, and Jochen Taupitz as vice chairpersons.

Members 2008–2012

Following the respective suggestions of the Bundestag and the Federal Government, the then President of the Bundestag Norbert Lammert appointed the following members on 15 February 2008, who represented the German Ethics Council until 2012:
During the German Ethics Council’s inaugural meeting, its members elected Edzard Schmidt-Jortzig as their chairman and Christiane Woopen as well as Eberhard Schockenhoff as their vice chairpersons.

Topics and Opinions

The Council usually decides on its substantive focus during the last meeting of each year, creating a working schedule for the subsequent months. Each topic is continuously discussed in the plenary sessions, the working groups, and dedicated public events. The working process for an Opinion normally stretches over several years. If, in the drafting process, members have a dissenting view, they may express this in the Opinion. After publishing an Opinion, the Council accompanies the corresponding political and societal debates and evaluates the reception of its recommendations by the general public.
In addition to the Opinions, the Council publishes Ad-hoc-Recommendations.

Anonymous relinquishment of infants

The Council’s first Opinion “Anonymous relinquishment of infants”, published on 26 November 2009, addresses the ethical and legal problems raised by facilities for anonymous birth. Considering the legal and individual problems associated with the facilities for anonymous relinquishment of infants, and in view of the unproven life-protecting effect of these possibilities, the German Ethics Council recommends abandoning these facilities. Instead, public information and institutional aid programs for pregnant women should be expanded considerably.

Human biobanks for research

The Opinion “Human biobanks for research”, published on 15 June 2010, discusses the ethical and legal issues arising in connection with human biobanks, ranging from the protection of individual rights to the global regulation of research infrastructures. In its Opinion, the Council proposes a five-pillar concept for biobank regulation. It includes recommendations on introducing biobank secrecy, on defining permissible use, on involving ethics commissions, on quality assurance and on transparency. It is the aim of the recommendation to provide a suitable legal framework for the interests and rights of personality of the donors, to achieve more legal certainty for biobank research and at the same time to facilitate research.

Medical benefits and costs in healthcare

The Council’s Opinion “Medical benefits and costs in healthcare”, published on 27 January 2011, deals with the question of the allocation of funds in the health care sector. Addressing this issue was a reaction to the inability of two Enquete Commissions appointed by the Bundestag to pass recommendations concerning this matter. Considering the impending cost increase in the health care sector due to medical progress with a simultaneous increase in life expectancy, the Council’s Opinion formulates recommendations based on the principle of human dignity and the accompanying fundamental rights that aim both at optimising the allocation of funds for healthcare and achieving equitable distribution of resources.

Preimplantation genetic diagnosis

In this Opinion, published on 8 March 2011, the Council comprehensively sets out the relevant factual position and the decisive arguments of supporters and opponents of permitting preimplantation genetic diagnosis. Against the background of current technological and legal developments, the Ethics Council describes the current practice and the new possibilities of genetic diagnosis of embryos. It goes into detail on the various positions and arguments on the status and protection of embryos and discusses the most important socio-ethical aspects. Due to differing views among the Council’s members, particularly concerning the status of embryos in vitro and thus the justifiability of PGD, the Council develops two alternative proposals for legislation on PGD.

Human-animal mixtures in research

In its Opinion “Human-animal mixtures in research”, published on 27 September 2011, the Council identifies the ethical challenges that arise from the creation of human-animal mixtures for medical research purposes. Such experiments call into question the biological species boundary between humans and animals. The Council considers it necessary to identify the ethical challenges that may be presented by the creation of human-animal mixtures and to determine where it may be appropriate to set binding limits. The Council concentrates its attention on the transfer of human material to animals, which it examines on the basis of three examples: cytoplasmic hybrids, formed by the insertion of a human cell nucleus into an enucleated animal egg; transgenic animals with human genetic material; and the transfer of human cells into the brains of fetal or adult animals. The Opinion presents recommendations on these examples.

Intersexuality

Upon request of the Federal Government, the Council dedicated its prepared the Opinion “Intersexuality”, published on 23 February 2012, to the situation of intersex people in Germany. It emphasizes that people with differences of sex development deserve respect and support; this implies that they need to be protected from undesirable medical developments, i.e. discrimination. The central issue in question concerns the admissibility of surgical procedures on sexual organs of people with DSD. If a person’s physical integrity requires an irreversible medical sex disambiguation or sex assignment measure, the relevant decision should always be taken solely by the individual concerned. In the case of a minor, such measures should be adopted only if absolutely necessary for safeguarding the child’s well-being and only after thorough consideration of all their medical, psychological and psychosocial advantages, disadvantages and long-term consequences. The Opinion further recommends that the compulsory binary classification of “male” and “female” in the civil registry should be ceased and non-binary people should be enabled to have registered civil partnerships.

Dementia and self-determination

The Council’s Opinion “Dementia and self-determination”, published on 24 April 2012, emphasizes the importance of respecting and encouraging the self-determination of people with dementia. It supports the Federal Government’s aim of developing a National Action Plan for dementia. The need for care of people with dementia should be reviewed by taking adequate account of their potential of self-determination. Outpatient communal housing and residential communities for persons with dementia should be expanded and the effort of caring family members more widely recognized as well as financially supported. The principles of the UN Convention on the Rights of Persons with Disabilities, which also includes persons with dementia, should be consistently applied to support their possibilities of self-determination.

Biosecurity

The Opinion on ”Biosecurity – freedom and responsibility of research”, published on 7 May 2014, discusses the issue of Dual Use Research of Concern, which describes research results in the life sciences that cannot only be used for the benefit of individuals and society, but  also misused with the intent to cause harm. To prevent such misuse, the Council recommends heightening the scientific community’s awareness of the danger of misuse, establishing a national biosecurity code of conduct to deal responsibly with research that may be open to misuse, and making funding of DURC contingent on approval by a new DURC Commission. Further, the Council recommends legally binding regulations and calls upon the scientific community and the Federal Government to promote the development of biosecurity codes of conduct for responsible research both within the EU and at a global level.

Incest prohibition

The Opinion on “Incest prohibition”, published 24 September 2014, evaluates, if, based on ethical reasons, a revision of the current legal situation on the grounds of Ethics is advisable. The Council aims for an open and unprejudiced discussion of the juridical and ethical issues arising in the context of close-relative relationships, focusing on consensual coitus between adults. Particular attention is given the case of sexual contact between siblings that share a family unit and bonds lived in practice no longer exist – a possible aftermath of a divorce or sperm donation for example. The evaluation is based on the weighing between clashing fundamental values, particularly how the right of sexual autonomy relates to the obligation to protect family structures. Concerning this matter, the Council could not find an unambiguous consensus: the majority would weigh the fundamental right of sexual autonomy higher, while the minority sees the protection of family as an entity as a priority and wants to uphold the prohibition of incest.

Brain death and decision on organ donation

An Opinion, published 24 February 2015, addresses the ethical and legal aspects concerning brain death and their implications regarding organ donation. Particularly, it deals with the questions whether brain death is a convincing criterion for a person’s death and whether brain death should be considered as a sufficient condition for the ethical and constitutional legitimacy of organ removal. The Council emphasizes the importance of transparency as well as an open public discussion in order to strengthen confidence in transplantation medicine. Further, it calls for improvements in information and communication and suggests amendments to the statutory regulations on organ-protective measures.

Embryo donation, embryo adoption, and parental responsibility

In an Opinion, published 22 March 2016, the Council presents recommendations regarding the legal regulation of embryo donation, embryo adoption and assumption of parental responsibility. The Council discusses the questions arising from the transfer of so-called surplus embryos to a third party for the purpose of carrying them out and assuming permanent parental responsibility. Namely it addresses the questions of children’s opportunities for life and development, parental responsibility, and family relationships. Taking special account of the child’s welfare, the Council considers it to be ethically necessary to legally specify the framework conditions of embryo donation and adoption. The Opinion contains several recommendations on how to deal with both.

Patient welfare as an ethical standard for hospital care

Growing economic pressure due to the cost development in the health care sector poses the question of the guiding normative criterion of hospital care. Addressing this issue, the Opinion, published 5 April 2016, identifies patient welfare as the guiding ethical principle for hospitals. It examines three dimensions determining patient welfare: patients’ self-determination, treatment quality, and distributive justice. The Council formulates recommendations that aim to enshrine and guarantee the orientation on patient welfare in hospital care, including for instance improvements in the areas of communication, documentation, digitalization, and accessibility.

Big data and health

The Opinion “Big data and health”, published 30 November 2017, examines the effects of big data processing on the healthcare system. Big data processing is characterized by the large volume and variety of data as well as the high velocity of its collection and processing,. Big data can improve diagnosis, therapy, and prevention; however, risks such as a loss of control over personal data arise. The Council examined these trends in a two-and-a-half year long process that involved extensive exchanges with experts and interested members of the public. The Opinion analyses the chances and risks of big data in five health relevant application contexts, evaluates the current legal framework and explores how values such as freedom, privacy, sovereignty, beneficence, justice, solidarity and responsibility can be guaranteed under big data conditions. The Council recommends a governance concept focusing on data sovereignty and makes specific suggestions to realise the potentials of big data, preserve individual freedom and privacy, safeguard fairness and solidarity, and promote responsibility and trust.

Benevolent coercion

In this Opinion, published 1 November 2018, the Council addresses the use of coercive measures in health and social services, including for instance the deprivation of liberty and medical treatment or care measures against a person’s will. If a person threatens to seriously harm him- or herself, coercive measures can serve a person’s welfare. Nevertheless, every instance of such "benevolent coercion" represents a serious infringement of the fundamental rights of the person concerned and is therefore in particular need of legal and ethical justification. Firstly, the Opinion is indented to raise public awareness of the problems and complexities around benevolent coercion. Secondly, it aims to draw the attention of politicians, legislators and practitioners to regulatory and implementation deficits and it formulates recommendations to remedy them. Thirdly, it intends to support the health and social professions in reorienting their self-image and their practice. The Opinion contains general recommendations for the responsible handling of coercion in professional caring relationships as well as specific advice for psychiatry, child and youth support services, and the fields of elderly and disability care.

Vaccination as a Duty?

Using the example of measles, the Council has examined which regulatory measures are ethically and legally acceptable to meet vaccination goals. In its Opinion, published 27 June 2019, the Council states that it is not a purely private matter, but rather a moral duty to have oneself and one’s own children vaccinated against a highly contagious infectious disease such as measles. However, the existence of this moral duty does not necessarily entail the justification of a legal obligation to vaccinate. At the time of publication of its Opinion, the Council considers such a mandatory vaccination policy only to be appropriate for personnel in the health, social and educational sectors. However, the Council recommends a number of other measures, which, taken together, could be suitable to close any remaining vaccination gaps and achieve the goal of eliminating measles permanently.

Intervening in the Human Germline

In its Opinion, published 9 May 2019, the Council examines whether interventions in the human germline could be at all justifiable and according to which criteria the ethical admissibility of specific applications can be decided. It examines the further research process necessary before any clinical application and three possible areas of application for germline interventions: the prevention of severe hereditary disorders, the reduction of disease risks and the targeted improvement of specific human traits or abilities. The analysis is based on eight ethical concepts: human dignity, protection of life and integrity, freedom, naturalness, non-maleficence and beneficence, justice, solidarity and responsibility. The Council members come up with seven unanimous recommendations, including a call for an application moratorium, but also the agreement that the human germline is not categorically inviolable. On many issues, however, there are different positions.

Robotics for Good Care

The research and development of robotic systems for home and in-patient care has received considerable public funding over the last couple of years. Political justification for this policy derives from urgent infrastructural, personnel and financial problems resulting from the increasing number of people in need of care and assistance and the worsening shortage of nursing staff. In its Opinion “Robotics for Good Care”, published 10 March 2020, the Council acknowledges the potential benefits of robotics for the entire care sector, but sees these benefits less in the elimination of staff shortages or the nursing crisis and more in its potential to promote good care. The realization of this potential, however, requires that the use of robots does not replace interpersonal relationships, that it is not used against the will of caregivers and people in need of care or merely to maximize efficiency, and that those affected by the techniques can also participate in their development.

"Reasonable" Treatment of Animals

The Council takes current debates as an opportunity to critically evaluate the treatment of livestock from a legal and ethical perspective. A working group has been established that will look at differences and discrepancies in dealing with and relating to different animals as well as at the obvious tensions between animal welfare regulations and certain aspects of agricultural practice. The aim of the project is to define more clearly both the protected goods at the heart of animal welfare regulation and the criteria according to which these may be curtailed in favour of other interests. Furthermore, the group aims to examine ways in which such a balancing of interests could be done more honestly and consistently in the future.

Ad-hoc-Recommendations

Since 2013, the Council has been publishing Ad-hoc-Recommendations in which it comments on current issues.
Ad-hoc-Recommendations have been published concerning the following topics:
In addition to the Opinions and Ad hoc Recommendations, the Council publishes Annual Reports, three times a year an “information letter”, studies and documentations, e.g. conference reports, documentations of consultations.

International exchange

The Council stays in close dialogue with its partner committees in other European countries. For example, trilateral meetings with the British Nuffield Council on Bioethics and the French Comité consultatif national d’éthique took place in 2009, 2012, 2016 and 2019. Meetings of the Ethics Councils of Germany, Austria and Switzerland were held in 2014 and 2017.
In addition, the Council hosted the under the Presidency of 2012-2016 Chair Prof. Dr. Christiane Woopen of Cologne University.