Exiting the European Union (Plant Health)

Daniel Zeichner Excerpts
Wednesday 2nd December 2020

(3 years, 4 months ago)

Commons Chamber
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Daniel Zeichner Portrait Daniel Zeichner (Cambridge) (Lab)
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I echo the Minister’s points about just how important these measures are. At first sight, they perhaps seem slightly impenetrable and very lengthy. The two instruments run to some 272 pages and 76 pages, and I doubt whether any of us has the energy or the expertise to be absolutely certain that everything is correct. As we have said in many other statutory instrument debates, it is probably only the people who are drafting them who really know that for sure. So there is always some cause for concern. On a personal level, I remember visiting the fantastic Sainsbury laboratory in the University of Cambridge a few years ago to be briefed on ash dieback. It is striking to see not only the excellent work that is being done to tackle these issues but the constant threats that we are facing. That is why it is so important that these controls are in place and that they are transposed in the correct way.

We are told that these two SIs have been laid using powers under the European Union (Withdrawal) Act 2018, and that their stated aim is to protect biosecurity and support trade by ensuring that effective phytosanitary controls continue to operate within GB and between GB and the EU at the end the transition period. We are also told that they establish the future plant health regime for Great Britain by ensuring that EU legislation related to phytosanitary controls is retained—and corrected as necessary, as the Minister has explained—to maintain the existing risk-based approach. The Animal and Plant Health Agency and the Forestry Commission will be delivering the measures in these regulations, and we are told that they are developing an implementation plan and that associated guidance will be published on gov.uk. We are also told that separate legislative arrangements will be needed for Northern Ireland in order to maintain alignment with sanitary and phytosanitary-related EU regulations and to specify requirements for GB goods entering Northern Ireland. Well, that is probably an understatement. I would echo some of the comments made by the hon. Member for Strangford (Jim Shannon), and I will return to that later.

The Government say that the amendments introduced are technical operability amendments and do not include any policy changes. That is what is said, of course, of many statutory instruments and we may beg to differ at some point. It appears that no impact assessments have been carried out, and that the regulations were not reported by the Joint Committee on Statutory Instruments and had not been raised by the Secondary Legislation Scrutiny Committee. As we have heard, the draft Plant Health (Amendment etc.) (EU Exit) Regulations 2020 make operability amendments to the retained EU plant health regulations, as well as consequential amendments to domestic law. The draft Plant Health (Phytosanitary Conditions) (Amendment) (EU Exit) Regulations 2020 defines at some length, as I have said, the list of regulated products and pests, and prescribes the requirements for entry and movement of regulated items into GB and within GB to reduce the risks in connection with those pests to an acceptable level.

Since the result of the European Union (Withdrawal) Act 2018 is that the UK leaves the EU single market, the operability amendments contained in this instrument create a single market covering GB and the crown dependencies. The EU will thus become a third country and, as a result, will be subject to third country import controls. The Government tell us that the current policy of risk-based plant health controls applied under EU legislation will continue, and that the GB risk assessment process will follow the same internationally accepted principles and approach used in previous pest risk analysis under the EU regime. Internal controls will also continue to apply to the movement of goods within the GB internal market.

We are also told that the revised approach for EU imports will be phased in over six months from 1 January next year, in the Government’s words, to

“stagger the operational implementation of controls on EU products to allow trade to continue to flow whilst businesses adapt to the application of third country import controls. This will be a temporary and risk-based transitional arrangement, with the aim of ensuring consistent and technically justified import controls which apply to all countries exporting to GB.”

The instruments also include a requirement to use UK rather than EU plant passports for intra-GB movements of plant-passported commodities. This will require businesses that move plant-passported commodities within GB to modify the reference code they use when issuing plant passports, replacing EU with UK. The process for authorising businesses with plant passporting, we are told, will not change. The Department for Environment, Food and Rural Affairs tells us that

“businesses who will need to use the system from 1 January 2021 are likely to already be registered. Therefore, we expect no extra impact on business from this change.”

Some questions follow from all of that. In 7.2 of the explanatory notes for the draft Plant Health (Amendment etc.) (EU Exit) Regulations 2020, it says that under these regulations our risk-based plant health controls will now

“focus on risks to GB, rather than risks to the EU”.

I was going to ask the Minister to explain what that means in practice. I think she has made reference to that already, but to repeat my question from previous debates around report and review, can she tell us when these policies will be reviewed and where that sits in relation to reviews already promised to be undertaken by the EU? Should the EU tighten their standards, would we be doing likewise and vice versa?

As I have said, Madam Deputy Speaker, these are very, very lengthy, detailed instruments. I am eternally grateful to Greener UK, which has found the time to look at them in some detail. It raises some points, as it often does, that I suspect the Minister may wish to write to me on, because they are detailed and I would not expect her necessarily to have an answer to hand. She may do—she may surprise me. Greener UK tells me that regulation 28(24)(c) changes the requirement in article 25(4) of EU regulation 2016/2031. This is in the draft Plant Health (Amendment etc.) (EU Exit) Regulations 2020—the first one, I think. Deep in that regulation there is a change for the UK to establish priority pest plans for all listed pests within four years of the 2019 EU regulation, to instead set a deadline of 1 January 2023. This is in line with the previous timescale. However, the clause also adds a line, 4A, disapplying that requirement to any priority pest removed from that list before the same date. While the intent behind that may be simply to clarify, it would be superfluous to create a plan for a pest that is no longer considered a threat. In the view of Greener UK, this explicit reference appears to potentially incentivise the late development contingency plans. It may well be that that is covered by some of the points that the Minister has already made about the differing threats that we face. However, will she outline the UK’s progress in developing such plans to date, clarify whether the Government still intend to produce such plans for further priority pests currently listed in the EU level, and provide any details on intended timescales? Will she also tell us whether the Government have any plans to change the current list after the end of the transition period and whether any changes will be subject to the same risk assessment process used currently by the EU?

On equivalence investigations, regulation 30(7) amends paragraph 2 of article 44 of regulation 2016/2031, and removes a reference to the Commission’s ability to carry out investigations in third countries to determine whether equivalence is being properly achieved. It does this without replacing it with a reference to an appropriate UK body. Determinations of equivalence in biosecurity and control measures will be vital to protect the UK’s natural ecosystems in future. This reference therefore appears unhelpful, and the reason for deletion is unclear. It would therefore be helpful if the Minister could explain the reasoning and outline how the Government propose to ensure the legitimacy of claims of equivalence from third countries, and whether investigations will form a part of this approach. That seems to me to be a rather important point. As I say, I do not necessarily expect an answer today, but it would be helpful to have one at some point.

The third point raised by Greener UK is on amending regulations. In a number of places, references in EU regulation 2016/2031 via article 107(2) to a specific examination procedure for scrutinising and adopting amendments to regulations, as contained in article 5 of reg 182/2011, are removed. The examination procedure was designed to provide an additional level of scrutiny to implementing decisions relating to specific areas of concern, including the environment, security and safety, or protection of the health or safety of humans, animals or plants. These references to the examination procedure are replaced now with a power to amend regulations that does not feature an opportunity for scrutiny. For example, reg 30(17) replaces a requirement to follow the examination procedure with:

“The appropriate authority may by regulations amend Annex 9 to the Phytosanitary Conditions Regulation where the amendment is appropriate in the light of a risk assessment in relation to a plant, plant product or other object.”

Removing a defined process for strong committee-level scrutiny—that is, us—and decision making and replacing that with a standard reference to the right of the appropriate authority to make regulations represents, in the view of Greener UK, an unhelpful weakening of oversight, and I rather agree. This will be particularly pertinent if the Government choose to pass future regulations via the negative procedure. Will the Minister explain why the EU examination procedure could not be replicated within the UK context to provide clear democratic oversight of amendments? Will she outline how the Government propose to ensure that levels of scrutiny for secondary legislation pertaining to

“the environment, security and safety, or protection of the health or safety, of humans, animals or plants”

will not be weakened as a result of these changes?

I am grateful to Greener UK for finding these detailed points. As I said, I do not necessarily require a reply today. I will conclude with some more basic questions. At paragraph 7.3 of the explanatory notes for the Plant Health (Amendment etc.) (EU Exit) Regulations 2020 we are told:

“This will be a temporary and risk-based transitional arrangement for plant health controls”.

How long is temporary, and how much risk, because I am not entirely sure that I like the sound of that? It sounds like an excuse to me.

There has been no impact assessment of these regulations on businesses, yet there are clear indications that businesses will be impacted. Under these regulations, the revised approach for EU imports will be phased in over six months from January 2021 to

“stagger the operational implementation of controls on EU products to allow trade to continue to flow whilst businesses adapt to the application of third country import controls.”

Businesses moving plant-passported commodities within GB will need to modify the reference code that they use when issuing plant passports from EU to UK, so why has there not been an impact assessment of these regulations? Is it really presumed that there will be no impact on businesses at all?

The logic of paragraph 12.4 of the explanatory notes for the Plant Health (Amendment etc.) (EU Exit) Regulations 2020 is, frankly, “Alice in Wonderland” stuff. It outlines the extra checks that will be done, which I applaud, but goes on to say that because they are a result of the terms of the European Union (Withdrawal) Act 2018 and therefore do not reflect a change in policy, there is no need for an impact assessment. Can the Minister explain whether there has been an impact statement somewhere else? If so, where?

Finally, as I suggested at the outset, the bald statement that

“For Northern Ireland, separate legislative arrangements will be needed in order to maintain alignment with Sanitary and Phytosanitary related EU regulations and specify requirements for GB goods entering Northern Ireland”

is an understatement. Could the Minister outline what those separate legislative arrangements will look like and when they will be ready?

As ever, there are many questions. Ensuring plant health really matters. We are an island, but sadly, we need to be careful, and that is why we have a body of established law. It should not be weakened in any way, and while there is no desire for unnecessary extra checks, we all benefit when we stay safe.