Exiting the European Union (Food and Agriculture)

The instrument also makes relevant changes to other specific technical pieces of legislation on individual types of food contact material. It will ensure that regulatory controls for food contact materials continue to function effectively after exit day, that public health continues to be protected, and that high standards of food safety are maintained. Consumers must be protected against potential adverse effects of exposure to some substances used in the manufacture of materials and articles that are in contact with the food that we eat. The instrument will ensure that the effectiveness of the controls that we have is maintained.

This instrument, and the other SIs that we are debating today as part of the fourth and final bundle, will transfer responsibilities incumbent on the European Commission from Ministers in the European Council to Ministers in England, Wales and Scotland and the devolved authority in Northern Ireland. It will also transfer responsibility currently incumbent on the European Food Standards Authority to the relevant food safety authority: the Food Standards Agency, for which I hold ministerial responsibility in England, Wales and Northern Ireland, and Food Standards Scotland north of the border. The change will also ensure a robust system of control to underpin UK businesses’ ability to trade both domestically and internationally.

Let me now say something about the impact of this instrument on industry. The proposed amendments are expected to have a very minimal impact on businesses that produce or use food contact materials or articles. Existing provisions have received very positive feedback from our previous consultations, and there is no evidence that the changes required will be detrimental to industry. I was asked about the devolved Administrations. They have consented to the instrument. We liaise closely at official level with our opposite numbers, and, as with the instruments that we have already debated, throughout this month we have engaged positively with the devolved Administrations throughout the development of these instruments. Let me place on the record again my thanks to them for their positive engagement with me and my team.

Returning to industry, no changes to the way in which UK food or feed businesses are operated or regulated will arise from this instrument. There will be a continuation of the robust authorisation system I have outlined, the labelling requirements I have touched on, and the controls for GM food and feed that UK industry is familiar with and relies upon. The instrument enables the continued use of GM food and feed authorised in the UK. Again, the devolved Administrations provided their consent for it.

Thirdly, the Novel Food (Amendment) (EU Exit) Regulations 2019 are another instrument to be made under the powers of the European Union (Withdrawal) Act 2018. Novel foods are those that are relatively new or do not have a significant history of consumption in the EU. Those foods must be assessed for safety before they are introduced into the market to ensure that they do not present a risk to public health. This instrument will ensure that the regulation of and controls on novel foods continue to function effectively after exit day and that public health is protected. Anything permitted prior to exit day will be permitted after exit day. The purpose of the instrument—which again makes no policy changes—is to rectify deficiencies in the retained legislation. So foods new to the market are not assumed to be safe; that is where we have decided to place the burden. In the interests of public health the regulations require novel foods to have a pre-market safety assessment to identify whether they pose a risk and how that risk could be managed. The regulations will ensure that the existing levels of public health protection and food safety are maintained.

The EU framework regulation on novel foods is supported by four implementing measures, which provide the detailed rules, data requirements and administrative procedures governing all novel products. This instrument will ensure that provisions in the four main pieces of EU legislation continue to function effectively after we leave. They will correct the following retained EU law: regulation 2015/2283, which is the main framework for regulation on novel foods; regulation 2017/2469, which provides administrative and scientific requirements for the applications; regulation 2017/2468, which provides administrative and scientific requirements concerning traditional foods from third countries, which of course there would be; and regulation 2017/2470, which establishes a Union list of novel foods. Finally, regulation 2018/456 establishes procedural steps for the consultation process to determine the status of novel foods.

I know that food businesses watch these proceedings with interest, and there will be no change in how they are regulated. The instrument will, however, ensure that the robust system of controls that underpins UK businesses’ ability to trade both domestically and internationally continues. Again, we have engaged positively with the devolved Administrations, and we have their consent for this instrument.

Finally, the Animal Feed (Amendment) (EU Exit) Regulations 2019, which concern feed law, are also made under powers in the European Union (Withdrawal) Act 2018. We are making necessary amendments to the overarching food and feed regulations under the powers in the Act, so that we continue to protect the public. The primary purpose of this instrument is to ensure that feed legislation continues to function effectively. The retained EU legislation on animal feed encompasses requirements relating to feed additives, feed hygiene, sampling—when local authorities do sampling, for instance—marketing, and the use of feed, including labelling.

This instrument will fix the inoperabilities in the retained EU legislation and provide a continuation of the legal requirements that already exist in EU law. These proposed amendments are equally crucial to maintain a functioning statute book and to maintain public safety and confidence. The instrument introduces a number of changes, but the purpose of them is to ensure that the animal feed regulations remain operable after EU exit.

Risk assessment responsibilities, currently incumbent on EFSA, will be assigned to the Food Standards Agency and, again, Food Standards Scotland north of the border, and again, we have had consent from the devolved Administrations.

These four statutory instruments are all necessary to ensure that our legislation relating to food and animal feed safety and hygiene continues to work effectively after EU exit day. No policy changes are being made. I hope the House will support the proposed amendments in these four instruments to ensure that continuation, and I commend them to the House.