That the Grand Committee do consider the Aquatic Animal Health and Plant Health (Legislative Functions) (EU Exit) Regulations 2019.
My Lords, I shall speak also to the instrument grouped with these regulations, as they are so interconnected. I should make it clear, first, that neither instrument makes any change to policy. These instruments are technical in nature and are to ensure a smooth transfer of powers from the EU to the UK. Secondly, I make it completely clear that these instruments in no way diminish our controls in the important subject areas covered. There is no proposal to alter or reduce our biosecurity controls for animals or plants, our animal welfare standards or our capacity to protect public health. Thirdly, Ministers will be able to make negative resolution statutory instruments only on specific procedural or technical matters that are laid down in the various legislative functions currently exercisable by the European Commission. The new enabling powers will therefore be confined to those matters that the European Parliament and Council have delegated to the European Commission to implement by way of tertiary legislation with input from relevant experts.
Legislative functions are currently conferred on the Commission by EU legislation. They enable the Commission to set out the technical details of the regimes in what is known as tertiary legislation. The two instruments take those powers currently held by the Commission and transfer them to the appropriate Ministers in the UK. These instruments are therefore correcting measures enabled by the European Union (Withdrawal) Act 2018. As I have said, the crucial point is that they do not introduce new policy. They preserve the current animal, fish and plant health regimes and simply ensure that we continue to operate effectively.
The Animals (Legislative Functions) (EU Exit) Regulations 2019 cover the area of animal health and welfare. They provide for legislative functions to be exercisable by UK authorities. The exercise of those functions will principally be by way of domestic secondary legislation by the appropriate authorities, made under the negative resolution procedure as they will involve minor technical amendments to the EU retained law. This instrument transfers existing functions currently conferred on the Commission in the areas of: animal transport—Regulations 2 and 6; livestock identification—Regulations 3 and 5; transmissible spongiform encephalopathies or TSEs—Regulation 4; seal products—Regulation 7; animal slaughter—Regulation 9; animal by-products or ABPs—Regulation 8 and 10; and zootechnical conditions— Regulation 11.
These functions include matters such as: amending implementation rules and procedures when amending detailed rules of sampling and laboratory methods; approval of new scientific disease-related tests; revisions to disease monitoring and surveillance; setting down rules for breeding programmes to recognise disease resistance in livestock; determining feed safety practices; amendment of training and educational programmes; and the uniform application of disease contingency plans. They also include the power to amend the welfare requirements for transporting live animals and methods of animal slaughter to take account of scientific and technical progress.
Regulation 12, “Saving and transitional provision” is a cross-cutting regulation applying across this instrument. It contains transitional and saving provisions relating to standard form documents. For example, although new forms will be introduced for the UK, under these regulations, it will also be permissible to use the current EU forms for several months after exit day.
Turning to the Aquatic Animal Health and Plant Health (Legislative Functions) (EU Exit) Regulations 2019, there is one matter which I wish to draw to your Lordships’ attention. This relates to the Explanatory Memorandum, which has been amended. The amended version, which was published on Monday, merely deletes incorrect references to powers not included in the SI, and therefore does not affect the content of the SI. The first was about editing the criteria for listing diseases. This was not included in the SI as the focus of this instrument is to ensure day-one readiness. The power to amend the criteria is not required to be transferred as the current criteria are well-established and effective. The second change involved the power to set out detailed rules for the introduction into the EU of aquaculture animals and related products from third countries. This was moved from this instrument to the Import of and Trade in Animals and Animal Products (Amendment etc.) (EU Exit) Regulations 2019, which contain a number of similar amendments. The detailed rules on imports into the EU are currently set out by the Commission in model health certificates, and the proposed amendments remove these model health certificates from retained EU law and allow the Secretary of State and the devolved Administrations to publish new health certificates for imports into the UK. I hope your Lordships will accept my apologies for any inconvenience or confusion. None of this affects this SI, but I wanted to be straightforward and open about the changes.
This instrument also provides for a series of legislative functions currently conferred by European Union legislation upon the European Commission to be exercisable instead by Governments in the United Kingdom. The difference is that this instrument relates to EU directives while the previous instrument covers EU regulations. Directives are transposed into domestic law by regulations or, in some cases, primary legislation, when they come forward, so they are already on the statute book. However, the functions conferred on the Commission in those directives were not transposed as it would not have been appropriate to do so, but they are now being brought in by these regulations to the appropriate Ministers in the UK.
My Lords, I thank the Minister for his introduction today, and his courtesy in providing us with a pre-briefing. I thank all noble Lords who have contributed to this discussion, and I refer to my entry in the register of interests. Like the noble Baroness, Lady Bakewell, we reiterate our concern about the process for dealing with these SIs. Once again, we register our concern about the reliance on powers being granted to the Secretary of State without external scrutiny and challenge.
It seems a bit of an act of desperation to produce these composite SIs, which have completely different subject matters, particularly when there are other SIs in the pipeline covering more specific regulations relating to these individual topics. In retrospect, it will make it very difficult for people to navigate their way through all these different bits of legislation and the different SIs.
I turn to the aquatic animal health and plant health SI. We accept that, for the most part, the substance of this SI is non-contentious, but I have a few questions. First, this instrument transfers a number of technical legislative functions to the Secretary of State, but it also refers to “appropriate authority” and “other responsible authorities”, suggesting that these powers may be sub-delegated. If that is the case, to which public bodies do the Government propose to sub-delegate these powers? Assuming that these powers will be sub-delegated, will the public bodies have to report on their use of the powers under the relevant provisions of the European Union (Withdrawal) Act 2018?
The second issue is on plant health. The SI transfers responsibility to the Secretary of State for import restrictions and bans on plants and plant produce, as well as emergency measures for restrictions on imports to prevent plant pests being imported. According to the Explanatory Memorandum, this power is conferred,
“in light of developments in scientific or technical knowledge or technically justified and consistent with the risk to plant health”.
So far, so good, but could the Minister clarify how these functions will be carried out by the Secretary of State, which organisations will be authorised to make that scientific or technical assessment, what will the status be of any advice given in these circumstances, and what additional resources will be required to carry out these functions previously carried out by the EU Commission?
Finally, I have a question relating to the controls on disease in aquaculture animals. In Regulation 6, on page 3, reference is made to adding, varying or removing an exotic or non-exotic disease from the proscribed list. Obviously, we want to make sure that diseases harmful to aquatic animals are controlled and are not inadvertently spread from the EU or third countries, but the circumstances in which these controls are put in place in aquaculture seem to concentrate solely on the adverse economic impact and the likely production or export losses. There is no reference to the welfare or suffering of the species involved.
I realise I am treading on a controversial issue here, but should the Secretary of State not have a wider responsibility to ensure good animal husbandry and a disease-free environment for these fish regardless of the economic consequences? I realise that this SI transfers current EU regulations, but is this something that the Minister will aspire to address when the opportunity arises? I hope that when he replies he will take into account the increasing evidence that fish that are farmed in an aquaculture environment that most closely replicates their natural environment are kept disease free and are less stressed, more productive and more robust in the longer term, so there is a longer-term benefit all round.
Turning to the Animals (Legislative Functions) (EU Exit) Regulations, again it would be helpful to know the appropriate authority in these regulations and the extent to which its advice is given independently and made public. I also have a few issues of detail to raise with the Minister. First, like the noble Lord, Lord Trees, I am concerned that the regulations on TSEs seem to water down the requirement in the annual monitoring programme to check animals in remote areas with low animal density. They also allow the overall programme to be revised based on a comprehensive risk analysis. Who will carry out this risk analysis and what organisations will be consulted before any changes are made?
The regulations also allow proteins derived from fish to be added to the feed of young ruminants based on a scientific assessment of their dietary needs. Will the Minister clarify who will be responsible for carrying out the scientific assessment? Does he accept that any relaxation of the current rules relating to TSEs should be made with extreme caution?
I refer the Minister to Regulation 7, which relates to the trade in seal products; I gave him notice of this question. As I read this regulation, it seems to water down our current ban on products derived from seal hunts. For,
“Commission shall adopt implementing acts”,
it substitutes,
“the Secretary of State may make regulations”.
It goes on:
“The Secretary of State may, by regulations … prohibit the placing on the market of seal products derived from seals killed as a result of a seal hunt conducted primarily for commercial reasons”.
What is intended to be achieved by that change and why do the regulations not spell out clearly a continued requirement to ban such products on the basis currently in operation in the EU? I look forward to his response on these issues.
My Lords, this has again been a very interesting and helpful debate. I understand that this is a subject that excites public concern and interest. The noble Baroness, Lady Bakewell, was concerned about future Secretaries of State. This instrument is about a very distinct area of operability. Changes of the sort the noble Baroness was envisaging would come through a completely different route. The work we are doing today is very technical and is about issues that the European Parliament and Council have defined as being for the Commission to manage. These instruments are very tightly drawn. Therefore, any changes of the sort that the noble Baroness might be envisaging are not in them because they are not about changing policies in the areas that have come up in these regulations.
I turn to one issue immediately. I can safely say to your Lordships that I am extremely concerned about TSEs and extremely cautious. The noble Lord, Lord Trees, and the noble Baroness, Lady Jones of Whitchurch, raised them. I want to make it absolutely clear that the TSE monitoring programme will not be watered down by the amendments; it will continue unchanged after we leave. Similarly, the Government have no plans to alter feeding stuffs regulations. These regulations exactly reflect the current EU programmes. Our existing monitoring programme for TSEs will remain at the current level, and we have no plans to change it. The Animal and Plant Health Agency is the national reference laboratory for TSEs and has the latest scientific evidence. I say that only to ensure that there is a recognition of the expertise that we have, as the noble Lord, Lord Trees, in particular, will know. Obviously one can never bind anyone else, but this is an area where, given what we have seen in a whole range of areas, we should always be extremely cautious.
As to whether there is any intention of loosening restrictions, the Government do not allow the feeding of fish meal to young ruminants and have no plans to alter that position. Again, any future changes would have to be based on a scientific assessment of the dietary needs of young ruminants and of the control aspects for permitting the young of ruminant species to be fed proteins derived from fish. However, as I said, this Government have no plans to alter the current situation.
I should have declared my farming interests and I apologise to your Lordships for not having done so.
Following the outbreaks of BSE and foot and mouth disease, which resulted from animal by-products entering the animal feed chain, in 2003 the EU implemented legislation to ensure the safe handling and disposal of animal by-products. The Government take very seriously the ever-present risk of the entry and spread of serious livestock disease. We all recall the pain and distress of those outbreaks. I can just remember the 1967 outbreak when I was at school. I was quite young, but I remember it very dramatically. There was also the foot and mouth outbreak in 2001. I want to be absolutely emphatic on this issue. Although this instrument has nothing to do with these matters in terms of the policy, which is not being changed, we simply must not and will not relax our guard. High standards of biosecurity are essential.
My noble friend Lady McIntosh and the noble Baroness, Lady Bakewell—I was going to say “my noble friend”—asked about rabbits and hares. Rabbit, and possibly hare, form a normal and much greater part of the diet in parts of the EU. There are currently no FSA-approved establishments for the slaughter of farmed rabbits or indeed hares—I have never even heard of hares being farmed. While the UK has a small rabbit farming industry, we are unaware of any commercial farms producing rabbits or hares for meat. Article 11 of directive 1099/2009 provides a derogation that currently allows farms to slaughter up to 10,000 rabbits, hares and poultry per annum outside an FSA-approved establishment, but there are currently no FSA-approved establishments here. This provision was brought back as part of that regime, but I am not sure it has a UK resonance. We have no plans to change any of the arrangements.