Animals (Scientific Procedures) Act 1986 Amendment Regulations 2012

Lord Taylor of Holbeach Excerpts

Thursday 13th December 2012 Grand Committee

Moved By

[Lord Taylor of Holbeach]

That the Grand Committee do report to the House that it has considered the Animals (Scientific Procedures) Act 1986 Amendment Regulations 2012

Relevant documents: 12th Report from the Joint Committee on Statutory Instruments, 14th Report from the Secondary Legislation Scrutiny Committee

[The Parliamentary Under-Secretary of State, Home Office (Lord Taylor of Holbeach)]

My Lords, the draft regulations amend the Animals (Scientific Procedures) Act 1986 to transpose European directive 2010/63/EU on the protection of animals used for scientific purposes. The new directive was adopted in September 2010 and came into force on 9 November 2010. It replaces directive 86/609/EEC, which is transposed into current UK legislation by the Animals (Scientific Procedures) Act 1986.

National legislation transposing the new directive must be implemented from 1 January 2013. The new directive has three main objectives: first, to rectify wide variations in the implementation of the previous directive by member states; secondly, to strengthen the protection of animals used in scientific procedures; and thirdly to promote the three Rs: strategies which replace, reduce and refine the use of animals in scientific procedures. It provides a practical framework for the regulation of animal research and testing in Europe and sets a benchmark for the rest of the world.

Many of the provisions of the new directive are similar to current UK legislation and practice. For example, the directive places a strong emphasis on minimising the use of animals and includes the promotion of the three Rs. We welcome the development of the directive because it will ensure that the framework in the European Union will reflect the structures that have worked well in the UK for the past 25 years, and should bring the rest of the European Union into line with those standards.

Some of its provisions are new or go further than current UK legislation. For example, the new directive extends protection to some invertebrate species—all cephalopods, including octopuses, squid and cuttlefish—and to animals bred primarily so that their tissues and organs can be used in scientific research. The new directive also requires member states to apply mandatory minimum standards of care and accommodation. There is a requirement for formal retrospective review of some types of project.

Other provisions are potentially less stringent than current UK requirements. For example, the 1986 Act, which we are amending, provides special protection for non-human primates, cats, dogs and horses. The directive extends special protection only to non-human primates.

Article 2 of the new directive allows member states to retain national provisions in force on 9 November 2010 that give more extensive protection to animals than those set out in the new directive so long as they are not used to inhibit the free market. We are making full use of this provision, as I will explain shortly.

A public consultation on the options for transposing the new directive was launched on 13 June 2011 and closed on 5 September 2011. Responses were received from more than 13,000 individuals and 98 organisations. The majority of responses supported the retention of current United Kingdom animal welfare requirements where these are stricter than those set out in the directive. Other responses suggested that we should use transposition to streamline regulation where this would not harm animal welfare.

The Government’s response to the public consultation was published on 17 May this year. It explained that we would retain most of our current, stricter, United Kingdom standards. These include: special protection for cats, dogs and horses; protection for immature forms of birds and reptiles; larger enclosure and cage sizes for dogs and a number of other species; and methods of killing animals that are more humane. We have also placed absolute bans on the use of great apes and stray animals of domestic species in the legislation. We believe that including and retaining these other stricter standards in the regulations is necessary and justified on animal welfare grounds and in order to maintain public confidence that animals used in experiments and testing will continue to be properly protected.

At the same time, we explained in the government response that we would simplify our system of personal licences, which authorise individuals to apply procedures to animals. We believe that a system of personal licensing is essential to ensure that procedures causing pain and suffering are applied to animals only by individuals who are properly trained and competent. At the same time, we accept that the system should not be overly bureaucratic. We have therefore made some small but important changes, through the regulations, to allow us to simplify the detail required in personal licences and the way we process applications for them.

Another important change transposed in the regulations is the requirement placed on member states to collect and publish statistical information on the severity of the procedures applied to the animals. Publication of information about the actual experience of the animals will be a major step forward in terms of transparency and, combined with the mandatory requirement to publish non-technical summaries of authorised projects, will help inform the debate on the use of animals in research and testing.

On the issue of severity classification, although the directive requires procedures to be classified by their severity, there is no requirement to ensure that these classifications are subsequently adhered to. Under current UK arrangements, licence holders are required to inform the Home Office if a severity limit is breached or likely to be breached. We intend to continue this requirement by retaining the existing condition on the project licence that sets a clear obligation to adhere to the severity limit and to notify the Secretary of State if the severity limit appears to have been, or is likely to be, breached. I can, therefore, assure noble Lords that we are not weakening the current requirement for project licence holders to ensure compliance with severity limits.

I will also give noble Lords an assurance as to how we will review the operation of the new legislation and, in particular, in relation to the application of the three Rs. Article 58 of the directive requires the Commission to carry out periodic, thematic reviews of the three Rs in consultation with member states. Although the obligation to carry out reviews is on the Commission, and does not require transposition in the draft regulations, we believe that similar reviews can play an important part in ensuring the effective operation of our national legislation. We therefore propose to carry out our own thematic reviews and to consult practitioners and other interest groups in due course on suitable topics. We will also encourage the Commission to ensure that Europe-wide thematic reviews become a reality.

Regarding implementation of the amended legislation, although we have not quite achieved the target date for transposition—we were looking at a November date—we are already working with current licence and certificate holders to ensure a seamless transition to the new arrangements. We have already issued a guide identifying a number of actions that need to be completed before 1 January. We also plan to issue a “quick start” guide to the main requirements of the amended legislation and the care and accommodation standards before Christmas. A full draft guidance note and revised code of practice will be published in January 2013 for consultation.

The transposition of the new directive has provided a valuable and timely opportunity to review and strengthen our legislation. We believe that the draft regulations provide a sound basis for the regulation of animal research and testing. I commend the regulations to the Committee.

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I hope that the Minister understands that, although the directive is welcome, there are concerns that we must retain the standards that we currently have in the UK, ensuring that there is no slippage. Perhaps he can double check and tell me today—or, if not, write to me—whether there is any area under the directive where we will not be maintaining our high UK standards, other than the one I mentioned.

[Lord Taylor of Holbeach]

My Lords, this has been a very productive debate in the sense that I have an enormous amount of paper in front of me. I hope that noble Lords will be patient, because if I can give answers, I will certainly try to do so.

I am very pleased that there has been a general welcome for the transposition. I am the Minister in the Home Office for this subject and also the Home Office Minister for transparency, and I think that there is a link between the two. We all recognise some of the difficulties that the industry and profession of animal experimentation has in communicating ideas to the public. What pleased me about a meeting I had the other day with the Society of Biology was the real willingness of scientists to recognise the need to communicate beyond their peer group, and even beyond those people who have a special interest in this area, to the public at large. I am sure that we all recognise that as being very helpful. It would help us; it would help the cause of animal experimentation; it would help drive the high standards that we have in this country.

It is a delight to hear from the noble Lord, Lord Winston, because no one is more informed than he is about some of these specialties. I am delighted that he was able to attend the debate. He asked me a number of questions, and I will do my best to answer them. I hope that noble Lords will prompt me if they feel that I might be able to communicate a bit more information, if not today, in writing afterwards.

Our position as a Government is that we understand that it is important to maintain our competitiveness in this important area of science. Science is an important industry in this country. We have centres of excellence which are of global standards and it is quite right that we do not put ourselves at a disadvantage to our competitors. The noble Lord mentioned that some animal experimentation is bound to be necessary, because non-animal models are not always good alternatives. He went into the reasoning behind that. I do not disagree. I think that it is essential to choose the right methods. We do no service if we do not examine that, and the regulations recognise that alternatives must be scientifically sound if they are to be used rather than animal experimentation. There is no point in trying to do it in an alternative way if that does not support the science that we are seeking to explore.

The noble Lord also mentioned the attractiveness of animal use for students and the importance of attracting high-quality PhD students to work in this area. We welcome the scientific community’s recent public commitment to the need for animal research. This will help improve public confidence in the way in which this work is done.

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[Lord Wills]

Would the Minister be prepared to meet me on that one point? Discussion about Section 24 has been going on for a very long time and, in my experience, there are always people opposed to transparency in every area of public life. I would very much welcome the opportunity to have a further exchange of views.

[Lord Taylor of Holbeach]

Certainly, and I hope that we will be able to arrange that in the new year. I think that that is realistic; we have few days left this year; but I am happy to do that. We might also discuss the Weatherall report and the primates strategy. We agree that it is important that the use of primates in research is appropriately monitored. We have made that clear in everything that we have said. We keep the Weatherall report under consideration at all times, but I cannot give a progress report. Perhaps by the time we meet, I might know the answer to the question about page 140. I will try to find it.

I move on to the comments made by the noble Baroness, Lady Smith. They joined up with the points made by the noble Lord, Lord Wills. I made it clear that the Animal Sciences Committee is being set up. It will be very similar to the previous committee, but we wanted to create a new committee and the directive requires us to have such a committee. As I said, we have recently advertised for a chair and members, including a member with expertise in ethics.

I have dealt with the question of timing. I have dealt with the guide. The noble Baroness, Lady Smith, was particularly interested in knowing in which particular areas standards have not been maintained or transposed. We are retaining all the higher UK standards in every case where it will ensure better animal welfare. If she feels that that is not the case in particular instances, I should be very grateful if she would let me know. That is certainly the objective.

[Baroness Smith of Basildon]

That is extremely helpful; I am grateful to the noble Lord. One of the specific instances I mentioned in my comments was about annexes to the directive on humane killing. I do not expect him to answer that today. I take the point that he has made, but if he could write to me on that, that would be helpful.

[Lord Taylor of Holbeach]

I can answer it today, because I have the answer here, I hope. We are not transposing Annexe 4 as it stands. We are amending our current ASPA Schedule 1 to retain more humane methods. There is no question of clubbing kittens or chopping the heads off sparrows. I can assure the noble Baroness that we will maintain those higher standards.

There is a clear commitment to prohibit the use of great apes; I think that I made that clear at the beginning, and that continues. We also agree that the current high cage and enclosure sizes are good for welfare, which is why we have maintained all those standards in the transposed regulations.

[Lord Alton of Liverpool]

Just before the Minister completes his remarks and sits down, I thank him for the offer of a meeting to discuss issues such as tetraploid complementarity and the other complex questions that he alluded to. Before that meeting takes place, would it be possible for his officials to prepare a note answering some of the specific questions that I put to him? For example, I raised the number of animal/human hybrid embryos that have been created; there were over 150 when I last tabled a Parliamentary Question about them. That kind of information would be very helpful in advance of the meeting that we are to have.

[Lord Taylor of Holbeach]

If I understand the noble Lord correctly, he indeed asked a question about actual numbers. I do not have them to hand but I am sure that they are available, and if we do not have them we will see if the Department of Health does. We will do our best to inform the discussion that we are going to have with a certain amount of preparatory work on the questions that he has raised.

[Baroness Warnock]

Before the Minister finally sits down, I would like to raise a question about the numbers that were just mentioned. Does the Minister think it possible to persuade the Home Office to classify the numbers that are published under headings not just of severity but of the purpose of the experiment? We are constantly told that the number of experiments is rising but the document admits that many of them cause no pain at all and are to do with breeding rather than experiments in the normal sense. In the days of the pre-1986 committee, repeated efforts were made to get the publication classified by purpose as well as severity, and I do not know whether that is still a possibility.

[Lord Taylor of Holbeach]

That is certainly something that we are considering. One of the advantages of being able to assess severity as well as numbers is that there are new opportunities for presenting the figures as well as in overall number terms. I do not think that that was quite the question that the noble Lord, Lord Alton, was asking, but I am grateful for the noble Baroness’s question because it has given me the chance to say that the way in which we present the numbers is something that we are looking at.

I am sorry that this has taken quite a long time, but it is an important aspect of an important issue and public interest is considerable. I hope that I have covered all the points but we will review the debate and see if there are any that I have not. Meanwhile, I commend the regulations to the Committee.

Motion agreed.