UK Parliament / Open data

Department of Trade and Industry

Indeed, I am happy to do so. We in this House benefit from having the experience of Members, such as the hon. Gentleman, who have been involved on the front line of science policy—Members who have served on the Select Committee and, as in the hon. Gentleman’s case, have also been Ministers with responsibility for science and have therefore received advice from such people as my constituent Lord May. I wish to raise with the Minister a couple of issues that were addressed in the report. There was a recommendation to do with the double-counting of non-scientific opinion. Scientific responses to consultations often put forward the science and then also say—as the Royal Society recently did in responding to the Government consultation on embryology, and especially inter-species or hybrid embryos—““This is the science, but we must of course bear in mind the fact that there will be public worries about it, so perhaps we should be cautious.”” However, the anti-science or non-scientific evidence—I do not use those terms pejoratively—often does not give any credence to the scientific side and says, ““We say 100 per cent. that we must not do this as it is wrong.”” Therefore when the scores are added up, there are one and a half bids for caution and only one bid for going ahead on the basis of the science. When there is considerable lay membership on scientific advisory committees, there is a danger that we get diluted scientific advice instead of pure scientific advice. So when the Government consider such advice along with that of other stakeholders—which is the right thing to do—the result is a dilution of the scientific message. The Government recognised that that was a problem and undertook to do something about it. Do they have any further thoughts on that? I wish to reinforce points made by my hon. Friend the Member for Harrogate and Knaresborough and the hon. Member for Bolton, South-East (Dr. Iddon), which were supported by the hon. Member for Esher and Walton (Mr. Taylor), about the future of the Science and Technology Committee. I should make it clear that some Members present have an interest in the subject as we are members of the Committee in question. However, there is a twofold danger in relying solely on a departmental scrutiny-type committee, regardless of how well it is chaired and does its work. First, there will be a tendency for it to be dominated by the university agenda, which is highly political. It is right that that should be so, as that is an important sector of public policy; it will flex its muscles both politically and in the media and by means of the institutions themselves. Secondly, and crucially, as with the Public Accounts Committee and the Environmental Audit Committee, in terms of science and technology there is a case for cross-departmental scrutiny of Government and Government agencies because that cannot entirely be invested in one Department. I hope that the Minister has established, and will develop, that important cross-departmental role. I ask him to share his thoughts on this matter—as far as he can, as it is subject to negotiation. Does he recognise the importance of there being a cross-departmental scrutiny role in respect of science and technology? I also seek elucidation from the Minister on the Government’s policy on publishing evidence. Page 17 of the Government’s response addresses the Science and Technology Committee’s recommendations 34, 35, 37, 50 and 51. The Committee’s report made it clear that evidence underpinning policy should be published. The Government response states that they will publish that except in respect of freedom of information and data protection legislation exemptions. If those exemptions cover advice to Government, that could catch all, or much of, the evidence that one would hope would be published when the Government produce a policy. To be fair, it should be added that the Government say that it is final advice to Government that would be caught by freedom of information legislation. The Government’s response states in paragraph 25 of the introduction:"““Inputs other than evidence…will influence policy outcomes””—" we have already accepted that. It continues:"““Nevertheless, where possible, the Government agrees that processes should be transparent and the balance of evidence exposed. Transparency may not be possible in reserved areas. Examples of reserved areas include advice that precedes a final policy outcome””." It is not clear to what extent that covers the evidence or the view taken of that evidence by a departmental chief scientific adviser, because the evidence is collected, the DCSA considers it and makes a recommendation to Ministers. It would be unfortunate if none of that process could be seen, especially the crucial latter stage. It is not clear from the Government’s response what their plan is in that regard. I shall not go into the areas of the report covered by my hon. Friend the Member for Harrogate and Knaresborough. I strongly support his concern about the loss of capacity and, therefore, the need for a Government scientific service. I also support what he said about trials and pilots. It is welcome that the report made it clear that there is an onus on Opposition parties not to attack the Government for responding rationally to a pilot or trial that does not work. If a pilot or trial is ignored, it becomes early implementation followed by roll-out, and that could lead to a great waste of money. The hon. Member for Norwich, North made several important points about the need for the scientific world to be quick on its feet. There is a dilemma between the need for rapid rebuttal and the need to ensure that the scientific process is not compromised by a rush to comment. The role of the science media centre has filled that gap to some extent, because it has experts on tap who, within the limits of their expertise and with care, can make a rapid response to a scare story, so we do not have to rely on the Royal Society and the Academy of Medical Sciences to set up a six-month working party to produce the definitive statement long after the story has taken off. The science world has understood that and that is why it funds the science media centre—it can redress the balance. The hon. Member for Esher and Walton made some important points about scientific capacity in the civil service, the understanding of risk and the way in which the media behave. The first newspaper I buy every day is the Daily Mail, because it is an excellent newspaper. Although I usually disagree with it on issues of policy and ethics, it transmits its message effectively and one can understand what is going on. Of course, its interest, and that of other papers, is in selling copies, and it will never have scientific accuracy as a priority. Nor will it be willing to recognise the problem that if there is one maverick with whom 99.9 per cent. of the scientific world disagree, the broadcast and the print media will tend to give both sides, which suggests to the public that there is a more even split. Politicians are in a privileged position, because they can think, take advice and try to find the scientific consensus on an issue. They do not have to jump on a bandwagon. MMR was handled correctly by the Government and I was pleased to support them 100 per cent. at the time. Some Conservative Front Benchers at the time—and I exclude the hon. Member for Esher and Walton—did not handle it correctly, because on public health issues there can be a high price to pay for political opportunism. Little could be done other than embark on the slow process of trying to explain to the media that the evidence for MMR causing autism simply was not there. While we cannot say that anything is 100 per cent. safe—and the Government were right not to try to claim that, because that is also a dangerous thing to say—the approach had to show that the evidence base was clear. The fact that Andrew Wakefield is now up before the GMC on charges of serious professional misconduct in connection with his research is an extra factor, albeit many years later, that suggests that those of us who considered the overall scientific picture—and not just the newspaper headlines—were right on that issue. The report mentions the precautionary principle and the problem of risk. We came to the view that the precautionary principle was an unfortunate phrase. Indeed, the chief scientific adviser said in evidence that the word ““principle”” seemed to imply some rule that whenever there was a potential risk, the Government had to respond. The Committee were right to applaud the use by the Government and the chief scientific adviser of the term ““precautionary approach”” and to make it clear that scientific progress must not be stopped because of a small potential risk. The report went further and said that the Government should lobby within the EU to change the terminology and approach taken by the EU—from the misunderstood term ““precautionary principle””, which means different things to different people, to a much more fleshed-out view of what we mean by a flexible precautionary approach. I was disappointed that the Government’s response effectively was to give up, saying that it was in too many international agreements and we would have to live with it. I think that the Government should advocate change in that area. In conclusion, I applaud the work by the members of the Committee, not including myself in this case. I also thank the hon. Member for Bolton, South-East for going into so much detail and clarity about the particular example of MRI, which was a good example that the Committee chose to take up. I hope that this important report will be one of a series of reports that the House will continue to receive from a cross-cutting Science and Technology Committee.
Type
Proceeding contribution
Reference
462 c1236-9 
Session
2006-07
Chamber / Committee
House of Commons chamber
Back to top