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Proceeding contribution from Lord Darzi of Denham (Labour) in the House of Lords on Wednesday, 21 November 2007. It occurred during Debate on bill on Human Fertilisation and Embryology Bill [HL].


Human Fertilisation and Embryology Bill [HL]

My Lords, I take this opportunity to remind the House that I am a member of many royal colleges and the Academy of Medical Sciences. More important, I remain an active clinical scientist and I am a recipient of funding from research councils. We have had a wide-ranging and extremely stimulating debate. We have heard some excellent speeches from all sides of the House. The issues raised demonstrate both the profound nature of the subject matter and the importance of proper scrutiny. We have seen a wide span of issues raised, including promising avenues of medical research and the welfare of children. As I have said previously, the United Kingdom has a good record of innovation and effective regulatory oversight, thanks in large measure to good parliamentary debates such as this. I shall do my best in the time available to answer as many as possible of the points that were made. I will not be able to do justice fully to all those issues in the space of one debate, but I am sure that there will be further in-depth discussions as the Bill progresses. On the need for public debate, a number of noble Lords, including the right reverend Prelate the Bishop of St Albans and the noble Lord, Lord Hastings, raised concerns about the pace of change and the Government rushing ahead with the legislation. We also heard concerns from my noble friend Lord Winston that we are falling behind. Several noble Lords mentioned the great importance of informed public debate on these complex and emotive issues. The Government agree that there should be a full public debate on complex ethical, moral and social issues, but we have tried to take as inclusive and as deliberative an approach as possible in our review of the legislation and the development of our proposal. As the noble Earl, Lord Howe, suggested, it is important that legislation keeps up with scientific advances and that the ethical implications are fully taken into account. The existing legislation is 17 years old and has served us well. It is, however, in need of updating and we have conducted a lengthy review process, resulting in the Bill before the House. There remains a general desire for a scheme of regulation with clear boundaries, but with a light touch. The noble Lord, Lord Winston, raised a number of important points about HFEA regulation, particularly the need for streamlined regulation of embryo research. The Government agree that it is important that research is not unduly delayed by the consideration of licence applications. The Bill gives the HFEA scope to introduce arrangements to enable licence applications to be dealt with more quickly. As the noble Lord indicated, these issues will no doubt be discussed in detail in Committee. On the filling of the vacant clinical academic chair previously held by my noble friend Lord Winston, I am sure that noble Lords will acknowledge that he is a mighty hard act to follow. Nevertheless, we will continue to strive to do so. Many speakers have talked about how bioethical issues are considered and debated. The noble Lord, Lord Brennan, spoke powerfully in favour of an independent bioethics commission. The noble Baronesses, Lady Neuberger and Lady Hooper, among others, raised the idea of a parliamentary standing committee to consider these issues. The Government have considered the idea of an independent commission on several occasions and have expressed their view that the present system, whereby a number of bodies are able to consider and advise on various ethical issues, is preferable. The Joint Committee that scrutinised the Bill also found that it could not support the idea of a bioethics commission. However, the Government share its view on the value of debating bioethical issues and the benefits of addressing complex issues in Parliament. As I hope noble Lords will appreciate, however, whether to establish a standing bioethics committee of both Houses, or whether the current structure is preferable, is ultimately a matter for Parliament itself. Beyond the domestic sphere, the noble Baronesses, Lady Williams and Lady Neuberger, asked about the Government’s position on attempts by the United Nations to ban reproductive cloning. The Government are prepared to support a worldwide ban on human reproductive cloning provided that it can be achieved without at the same time attempting to ban therapeutic cloning for legitimate research. Previous attempts at forming a UN resolution have foundered on this point. I say in response to the noble Baroness, Lady Hooper, that the UK has not ratified the Council of Europe Convention on Human Rights and Biomedicine. One problem is that that convention does not allow the creation of embryos for research and would therefore conflict with UK legislation. On adult stems versus embryonic stem cell research, there has been a significant debate—particularly from the noble Lord, Lord Alton of Liverpool, and the noble Baronesses, Lady Williams and Lady O’Cathain—around why we need to use embryonic stem cells in research when we can use adult stem cells. Several speakers referred to the work of Professor Wilmut, who has made a great contribution to stem cell research, which has also been eloquently described by my noble friend Lord Patel. He is, of course, right that all avenues of research should be explored. Let me be clear: the Government wish to see research using all sources of stem cells, including adult, umbilical cord and embryonic stem cells. Stem cell research offers the potential to deliver numerous new treatments for diseases as diverse as Parkinsonism, diabetes and heart disease. It is far too early to know from where useful results will come. This position is supported by the published scientific findings and informs the legislation and the decision-making of the HFEA. The noble Baronesses, Lady Williams and Lady Barker, asked about the funding of adult stem cell research. From 2004-05 to 2005-06 the Medical Research Council provided funding of £14.7 million for adult stem cell research and £16.5 million for embryonic stem cell research. Several noble Lords, including the right reverend Prelate the Bishop of Newcastle and the noble Lord, Lord Elton, raised the issue of the creation of interspecies embryos for research. The 1990 Act provides a legislative framework for the regulation of research projects, including human embryos, in accordance with the legal limits. One of those limits is the prohibition of the mixing of human and animal gametes that could result in the creation of true hybrid embryos. Otherwise, the current legislation does not explicitly mention any form of interspecies embryo. The Government have sought to address that. In the 2006 White Paper, following the development in the potential creation of interspecies embryos for research, the Government stated that the revised legislation would clarify the extent to which regulation would apply to embryos containing both human and animal material. The report of the Joint Committee that scrutinised the draft Bill very helpfully moved this debate forward. The committee recommended greater scope for discretion for the regulator and that the creation of a range of interspecies embryos, including true hybrid embryos, should be brought clearly within the regulator’s licensing remit. The Government have revised the Bill in order to put the proposal to Parliament for wider debate. The Bill brings some interspecies embryos within the scope of the regulator where licences may permit their creation subject to the requirement that the project is necessary or desirable for the purposes described in legislation. Additionally, subsection (5)(e) in proposed new Section 4A contains a regulation-making power to extend the definition of interspecies embryos. This will provide future flexibility to ensure that the law keeps pace with technological developments. The noble and learned Lord, Lord Mackay, asked what the Government mean by interspecies embryos. The definitions in the Bill are intended to ensure that embryos at the human end of the spectrum of research involving the mixture of animal and human material are clearly within the HFEA regulatory remit. The Government have discussed the available approaches with representatives from a number of professional bodies, including the Academy of Medical Sciences, the Royal Society, the Medical Research Council and the Wellcome Trust. On a more technical drafting point, the noble and learned Lord asked whether Clause 4(2) and Clause 3(2) are both needed. Clause 4(2) prevents any embryo other than a human embryo being implanted in a woman. This is to prevent animal embryos being implanted. Clause 3(2) limits the type of human embryo that can be implanted to a permitted embryo created by the fertilisation of a natural egg by natural sperm. The clauses prevent different things to make it clear that no animal embryo can be implanted in a woman and that only certain types of human embryos can be implanted. Many speakers, including the most reverend Primate the Archbishop of York and the noble Baroness, Lady Deech, have mentioned the child’s need for a father. I hope that I may be able to address some of the concerns through further explanation of the Government’s thinking. Many of the concerns raised appear to be motivated not by any practical effect that the clause may have in relation to assisted reproduction but by a general concern for the perceived signal or message that may be derived from its removal. I understand that concern. Let me say at the outset that the proposal is not motivated by any attack on fathers or on the concept of fatherhood. Nor is it motivated by a simplistic desire for political correctness. The Government recognise clearly the extremely important role that fathers can and do play in their children’s lives and the consequences that can follow where a relationship breaks down. Many measures taken by this Government are aimed at strengthening the role of fathers and ensuring that they are aware of their responsibilities. However, today’s debate deals with a very specific context: a fraction of the fewer than 1.5 per cent of births in the UK that result from licensed assisted conception treatments. Hence, we are talking about a few hundred children. The issue is what duties the state imposes on clinicians regarding whom they may or may not treat, or whether access to services—including those purchased privately—should be easier or harder for certain groups of people. Naturally, that will involve us considering our own individual views, to which we are well entitled, on the desirability of different family forms. However, unless the law is to be purely rhetorical, we must look at what is the intended outcome and whether it is justified by evidence. The duty to consider the welfare of the child is subject to the HFEA guidance, which states: "““Where the child will have no legal father the treatment centre is expected to assess the prospective mother’s ability to meet the child’s/children’s needs and the ability of other persons within the family or social circle willing to share the responsibility for those needs””." There is no ban on single women or same-sex couples receiving assisted conception treatment. There is no requirement in the law as it stands that there must be a father or any man involved in the upbringing of the child. The outcome intended to be achieved by the current law is therefore extremely unclear—or, as the noble Baroness, Lady Warnock, said, ineffective and wishy-washy. Undoubtedly, we want anyone contemplating having children to think through the implications. Given the nature of the procedures in question, we are talking about people who will almost invariably have considered very carefully their decision to approach treatment services and who will have decided to act responsibly. In addition, the law requires the provision of information and an offer of counselling. We must also remember that from a medical standpoint there may be no need to involve the services of a clinician at all. Informal arrangements for artificial insemination can take place. We must be careful that there is no perverse incentive for some people to avoid regulated services and the quality and safety assurances that they provide. The Government propose to retain the overarching requirement to consider the welfare of the child, which in practice, following consultation by the HFEA, focuses on the likelihood of serious harm to the child. In relation to fathers, there is clear evidence of poorer outcomes for children where a marriage or partnership breaks down and the father is then absent. It is right and proper that that should be addressed. However, in the context that we are discussing today, the available research evidence suggests that it is the quality of parenting that is the factor of prime importance, not the gender of the parent per se—a point strongly emphasised by my noble friend Lady Hollis. Elsewhere in the Bill there are provisions to extend legal parenthood in cases that recognise the family forms that already exist in practice, if not in law. The Government came to the view that, on balance, the reference in the 1990 Act to the need for a father should be removed in favour of the general duty to consider the welfare of the child. This does not prevent us from valuing the role of fathers in their children’s life, but it recognises the crucial role played by all parents. The noble Earl, Lord Howe, talked about saviour siblings, where the issue of children’s welfare arises very clearly; the noble Lord, Lord Alton, mentioned the definition of other tissue in relation to saviour siblings; and the noble Baroness, Lady Jay, mentioned the advances in the pre-implantation genetic diagnosis. The Bill does not limit which tissue can be used in the treatment of a sibling. However, the HFEA retains the control of tissue typing via licensing, and the Human Tissue Authority must approve any transplants involving organs from living donors and for children who are too young to give consent. The noble Lord also asked why the Government changed the criteria from life-threatening conditions to serious ones. The pre-legislative scrutiny committee recommended that the Bill should not be limited to life-threatening conditions but should also include serious conditions. There has been some debate around abortion. I thank the noble Baronesses, Lady Tonge, Lady Emerton and Lady Williams, and the noble Lord, Lord Alton, who acknowledged that abortion is a separate issue and that it would not be appropriate to use the Bill to amend the law on abortion. I recognise that different views are held, and held strongly, but we do not want to cloud the debate or hinder the passage of this important Bill by debating matters that are unrelated to its substance. This has been a very good and illuminating debate. The Bill has already benefited greatly from the pre-legislative scrutiny and I am glad that so much experience and expertise are being brought to bear to ensure that the legislation is as good as it can be. I look forward to the debate to follow on the very important issues that it covers. I commend the Bill to the House. On Question, Bill read a second time, and committed to a Committee of the Whole House.


Secondary information

Type
Proceeding contribution
Reference
696 c865-70 
Session
2007-08
Chamber / Committee
House of Lords chamber
Subjects
Disability Clones Abortion Breast cancer Cancer Civil partners Fertility Homosexuality Human embryo experiments Diseases Ethics IVF Fathers Northern Ireland Parents Minority groups Medicine Religion Research Stem cells Human-animal hybrid embryos
Legislation
Human Fertilisation and Embryology Bill (HL) 2007-08
Link
View this Proceeding contribution on www.publications.parliament.uk