Information on legal requirements concerning food hygiene for food businesses.
Food businesses must register with their local council and comply with food law.
You must register your business with the environmental health service (EHS) at your local council at least 28 days before opening. Food operations include:
You may also need to have your business approved if you supply another business with:
For information on how to register, contact the EHS at your local council. They can also advise you on the food hygiene law, and how it applies to your business in practice.
Food safety enforcement officers from your local council will inspect your business to make sure you are complying with food hygiene law. Inspections are usually unannounced.
Where necessary, inspectors can take enforcement action to protect public health, including:
Find out what to expect from a food safety inspection.
Food hygiene regulations set out requirements covering all aspects of your business. You must make sure that:
Depending on the nature of your business, you may also need to keep written records of how you manage food safety hazards.
You must put food safety management procedures in place based on the principles of HACCP (hazard analysis critical control point). In practice, this means that you must have documented procedures to manage food safety hazards in your business.
In March 2021, the EU adopted Regulation (EU) 2021/382 which introduced 'food safety culture' into the main EU food hygiene law.
This new requirement means food businesses in the EU must build a culture where everyone, from management to staff, understands and prioritises food safety in their everyday work.
Because the UK had already left the EU by the time this update was made, it doesn’t apply in Great Britain. However, under the Windsor Framework, EU food safety laws (including this update) still apply in Northern Ireland.
So, in practice, food safety culture is a legal requirement in Northern Ireland, but not in Great Britain. Local councils in Northern Ireland can look at how a business promotes food safety culture when they carry out inspections or other official checks.
Guides such as the Safe Catering Pack, Safer food better business and industry guides will assist you in meeting food hygiene legal requirements.
Follow good cleaning practices to help prevent food poisoning from occurring through cross-contamination.
Cleaning, disinfection and preventing cross-contamination are essential to make sure the food you serve is safe to eat, and to prevent food poisoning.
Effective cleaning, and disinfection where necessary, removes bacteria from hands, equipment and surfaces. This helps prevent harmful bacteria spreading onto food. You should:
Hand washing is a key part of food hygiene. Anyone who handles food must wash their hands:
Download hand-washing guidance (PDF, 572KB).
Cross-contamination happens when harmful bacteria spread from food, surfaces, hands or equipment onto other food. It is most likely to happen when:
For example, storing raw meat above ready-to-eat food in the fridge can contaminate the food below.
To prevent cross-contamination in your business, you should:
Guidance for food businesses on preventing food poisoning by ensuring food is properly cooked and chilled.
Cooking and chilling are both essential to make sure the food you serve in your food business is safe to eat, and to prevent food poisoning.
Thorough cooking at the correct temperature kills harmful bacteria in food. You must not serve food that is not fully cooked. You should serve cooked food immediately or keep it hot until serving. If you're cooking food in advance, cool and chill it quickly.
It is important to make sure that you fully cook:
These foods must not be served pink or rare, as they could harbour bacteria if undercooked. These foods should be steaming hot all the way through.
Whole cuts of beef and lamb, such as steaks, cutlets and whole joints, can be served pink or rare as long as they are fully sealed on the outside.
Chilling food to the correct temperature stops bacteria from growing. The Food Standards Agency recommends chilling food at 0-5 degrees Celsius. Chilling food below 8 degrees Celsius is a legal requirement.
You must keep some foods chilled to keep them safe. For example:
You should always:
Food handling hygiene and fitness to work in the food industry, including food-related illnesses and symptoms.
Anyone working with or near open food who has certain infections - bacterial or viral - must take precautions to prevent contamination.
Staff handling food or working in a food handling area must immediately report symptoms such as diarrhoea and/or vomiting to their manager. These symptoms are associated with illnesses that can be transmitted through food.
You must not allow anyone with these symptoms to work with or around open food, usually until 48 hours after symptoms have stopped.
Food business operators should follow guidance from the Food Standards Agency on good hygiene practices in food preparation and Hazard Analysis and Critical Control Point (HACCP) processes.
Anyone who handles food and works around open food must wash and dry their hands thoroughly before handling food or touching surfaces likely to come into contact with food. Food workers must always wash their hands after using the toilet. People can carry infection even if they do not show symptoms.
Read more about cleaning, disinfection and preventing food cross-contamination.
Food safety myths and whether they are true or false - including best before dates, rare meat and washing raw chicken.
This section addresses common misunderstandings that can lead to unsafe food practices. Businesses should rely on food hygiene law and recognised guidance, not myths, when handling food.
The Food Standards Agency has compiled a list of common questions and answers to dispel any food safety and hygiene-related myths.
False - it's a myth
Although a bad smell or taste can indicate that food has 'gone off', these signs often aren't caused by germs that give you food poisoning. So the food's appearance, smell or taste aren't reliable warning signs. Instead, stick to the 'use by' date and storage instructions on the packet.
True - it's a food safety fact
'Best before' dates are about food quality, not safety. They are usually found on food that lasts a long time. If food has passed its 'best before' date, it doesn't mean it's unsafe, but it might have started to lose its colour, flavour or texture.
False - it's a myth
A 'use by' date tells you how long food will stay safe. They have to be put on food that 'goes off' quickly - and they aren't just guesswork; the dates are worked out by scientific testing. Don't be tempted to eat food after the 'use by' date on the label, even if it looks and smells fine.
False - it's a myth
We've all been there! That delicious slice of cake slips from your fingers and lands on the floor, and you think surely it will be ok if I pick it up quickly enough? Well, unfortunately - no! However quickly you manage to retrieve it, any contact with the floor is long enough for the food to pick up nasty germs.
False - it's a myth
There isn't any strong evidence that one type of chopping board is more or less hygienic than another, whether plastic, wooden, glass or even marble. What is important is that the board gets cleaned properly after every use and is replaced if it gets damaged, for example from deep cuts or scoring. You could also use separate chopping boards for raw and ready-to-eat foods.
True - it's a food safety fact
Although most raw meat will have some germs on it, washing won't get rid of them. In fact, washing is more likely to spread germs around the kitchen. Little splashes of water can contaminate you, your worktops and anything else in the way. Thorough cooking is the only way to get rid of these nasty germs.
False - it's a myth
It's natural to suspect the thing you ate most recently would be the cause of food poisoning, but that isn't always the case. Symptoms usually take between one and three days to develop, so it won't necessarily be from the last thing you ate.
False - it's a myth
There's no specific evidence that food eaten out is more likely to cause food poisoning than food prepared at home, but it's easier to blame someone else. The habits we pick up from friends and family don't always ensure food is produced safely at home. As well as expecting good hygiene standards when eating out, we should also think about how to do things better at home.
False - it's a myth
Although most cases of food poisoning are mild and last only a day or two, some can be far more serious, even deadly. Thankfully this is rare, but with more than a million cases of food poisoning each year, 20,000 of which require hospital treatment, every case is worth avoiding. Avoid food poisoning by remembering the simple 4Cs for good food hygiene: cleaning, cooking, chilling and cross-contamination.
True - it's a food safety fact
Steak is safe to eat 'rare'. Whole cuts of beef or lamb, such as steaks, cutlets and joints only have germs on the outside, so as long as the outside is fully cooked any germs will be killed. But this isn't true for poultry, pork, burgers and sausages, these must be cooked all the way through.
False - it's a myth
Unlike steaks, burgers and sausages are made from meat that has been minced, so germs will be spread throughout the product and not just on the surface. This means these products need to be properly cooked all the way through. To check if a burger is done, cut into the thickest part and check there is no pink meat, it is steaming hot and juices are clear.
True - it's a food safety fact
Leftover cooked rice is fine to eat as long as it gets cooled and refrigerated quickly after cooking and eaten within 24 hours. This is because rice can contain a particularly tough type of bacteria that can survive heating. Most other leftovers are safe to eat up to two days after cooking. Always reheat leftovers until steaming hot and do not reheat more than once.
Why caterers need to be careful when they use eggs and how to prevent the spread of salmonella bacteria.
You should store, handle and prepare eggs carefully to prevent the spread of salmonella bacteria. Bacteria can be on the shell or in the egg itself, and can spread to other foods if eggs come into contact with them (or with hands and cooking utensils).
Salmonella can cause serious food poisoning, particularly in vulnerable groups such as:
To prevent risks associated with salmonella food poisoning, food businesses should:
Follow these ten key steps to prevent cross-contamination and food poisoning in your business.
Cross-contamination is when bacteria spread between food, surfaces or equipment. It is one of the most common causes of food poisoning. Use this quick checklist every day to minimise food hygiene risks in your business.
For more advice, read about food hygiene and the law.
Measures you must take to make sure food produced by your business is safe to eat.
When you start a food business, you must register with the environmental health service at your local council at least 28 days before you start trading. Registration is free of charge.
Register your food business online.
Most types of food business will need to register, including:
When you register your business with your local council, they will advise you on safety requirements and inspections.
If you run a food business, it is your responsibility to ensure that your food is safe, ie not harmful to health or unfit to eat. You must ensure that you keep food preparation areas clean and handle food in a hygienic way.
Important food hygiene and safety considerations can be remembered as the 'four Cs':
Make sure that you keep surfaces and utensils that come into contact with food clean and disinfected where necessary. Ensure that staff wash their hands regularly.
Make sure that you serve foods hot and thoroughly cooked. You should not serve products such as sausages and burgers, and meats such as pork and chicken rare or pink in the middle; when pierced with a knife any juices should run clear, not bloody. As an alternative check, you can cook food to a safe core temperature, for example 75°C for 30 seconds or an equivalent time and temperature combination. Once cooked, you must keep the food covered and hot (above 63°C) to prevent the growth of food poisoning bacteria.
Do not put hot food directly into the fridge or freezer, let it cool first. Make sure that food cools within two hours of cooking and that refrigerators and freezers can store foods at the right temperatures.
Keep raw foods separate from cooked and ready to eat foods at all times. Use separate chopping boards and utensils for raw and ready to eat foods. Wash hands after handling raw foods and before touching other foods and utensils.
You are responsible for monitoring the hygiene and safety levels in your business, in areas including:
You should make sure that food handlers involved in your business receive training in food hygiene that is appropriate to their role. Training should cover areas such as:
The level of training needed will depend on the type of work being done. You should also train staff in food contamination accidents and incident reporting, and they should be ready to follow emergency procedures if needed.
The Food Standards Agency (FSA) provides fitness to work guidance to help managers and staff prevent the spread of infection. The guidance advises which illnesses and symptoms staff should report and explains what managers should do in response.
It is important to have suppliers that you can trust to handle food safely. You should find out if your suppliers:
Make sure they give you accurate product information and specifications, particularly about allergenic ingredients.
Under the Food Safety (Northern Ireland) Order 1991 and European regulations, you must make sure that you give customers accurate descriptions of your food. This includes menus, labelling and advertising. Information given to customers must not be misleading.
If you move pre‑packed retail food from Great Britain to Northern Ireland, there are special movement and labelling rules under the Windsor Framework and the Northern Ireland Retail Movement Scheme. Check the latest official guidance to see if these rules apply to your business.
Keeping accurate records will help you comply with your legal requirements. The level of record keeping required will depend on the nature and extent of your food business.
The FSA guides such as the Safe Catering and Safer Food, Better Business packs will help you meet your legal duties and your responsibilities in areas of food safety management procedures and food hygiene regulations.
Find out what action the food safety inspector can take when inspecting your food business.
Authorised officers from your local council will visit your premises to check that your business is complying with food law and that you are producing food that is safe to eat.
The frequency of inspection will depend on the level of risk, the type of business and its previous record. Some premises might be inspected at least every six months, others much less often.
Authorised officers usually do not make an appointment. They have the right to:
The inspection may take place in the following circumstances:
Authorised food safety officers must show identification when they arrive. They should always give you feedback on an inspection and you can ask them to explain any issues or actions they identify. The inspection must follow the framework agreement on local council food law enforcement as set out by the Food Standards Agency (FSA).
It must also follow the Food Law Code of Practice, which states that inspectors should:
Food inspectors should also distinguish between:
During the visit, the food inspector might take samples and photographs of food. They may inspect your records or remove suspect foods. Following their visit, they might write to you informally asking you to put right any problems they found.
Where the Food Hygiene Rating Scheme applies, the findings from the inspection will be used to decide your food hygiene rating.
What happens following a food safety inspection, including enforcement actions and notices.
Food safety officers can take enforcement action against your business to protect the public. The officer should confirm any action you need to take in a written letter. They must give you enough time to put actions into effect, unless there is an immediate risk to public health.
During an inspection of your business, an officer can also serve a legal notice.
Examples of notices you may receive during a food safety inspection include:
This sets out what you must do to comply with food hygiene law. You may receive this if your business is breaking the law, for example where there are ongoing cleaning or structural problems.
This sets out what you need to do to comply with food information law. You may receive this if your business is breaking the law, for example where allergen information is missing or incorrect.
This forbids you to use certain processes, premises or equipment and must be confirmed by a court. Once confirmed by the court, it becomes a HEP order.
This forbids the use of certain processes, premises or equipment. It can also impose conditions on how you carry out a process. It's similar to a HEP notice, but it does not need to be confirmed by a court.
It is a criminal offence not to comply with a notice once served.
In serious cases, inspectors can also recommend prosecution. If a prosecution is successful, the court may forbid you from using certain processes, premises or equipment. It could ban you from managing a food business, eg via a food business prohibition order. It could also lead to a fine or imprisonment.
Some formal notices can be appealed. The documents you receive should explain whether you can appeal and how to do it, and you can read more in the section on how to appeal against a decision.
What to do if a food safety officer takes action against your food business.
If a food safety officer finds problems with your food business, they will itemise the issues in writing to you. They will give you a reasonable amount of time to make changes unless there is an imminent risk to public health.
Once you comply with the changes, inform the food officer immediately. This helps to minimise disruption to your business and can support any request you make for a revisit or re-rating where the Food Hygiene Rating Scheme applies.
You should keep evidence of the action you have taken, such as photographs, invoices, updated procedures or training records, in case the officer asks to see it or you later request a re-rating.
If the officer has removed the food for analysis or examination, you should check with them for the results.
If you become aware of a food incident - for example, your food has become contaminated - you must immediately remove your food from sale or recall it from customers. You must also notify the authorities immediately.
How to appeal against action taken by food safety inspector against your food business.
If you disagree with a decision made by a food safety officer, you should first discuss this with the officer. If you are unable to resolve the issue with the person you have been dealing with, ask them for the name of their manager. You can then ask to speak with them, or write to them if you prefer, to see if you can resolve the issue.
If you still disagree after this process, you should use the local council's complaints procedure to escalate your problem. If this doesn't resolve the issue, you could approach your local councillor or contact the Northern Ireland Public Services Ombudsman.
You can appeal further if you are dealing with:
The documents you received with the notice should contain guidance on how to appeal, including how long you have to do it. You should check and keep to any appeal deadlines in those documents.
See The Food Hygiene Regulations (Northern Ireland) 2006 for details on the appeals.
Where food is found to be unfit for human consumption, the food will be seized and presented to a Justice of the Peace for condemnation. You have a right to claim compensation if the court decides that:
The Food Standards Agency provides detailed guidance on how to appeal against a decision made by a local authority after inspecting your business.
Orla Smyth, Owner of Belfast-based Kaffe O, explains how they approach food hygiene and safety to achieve a food hygiene rating of five.
Kaffe O is a Scandinavian-inspired café business with multiple sites in Belfast. They have achieved the highest possible food hygiene rating of five.
Owner Orla Smyth explains how they have created a culture of prioritising food hygiene and safety throughout the business. Orla describes the approach they take to food hygiene, including staff training, audits and checklists.
Christina McErlean, Food Safety Environmental Health Officer at Belfast City Council, outlines the food hygiene inspection process and the Food Hygiene Rating Scheme. Christina explains the three areas evaluated during an inspection and what happens following a council's assessment of a food business.
If you sell or supply food, you need to follow strict rules on using colours and additives in foodstuffs, including those linked to hyperactivity in children.
Colours and additives help make and preserve food and drink products, but you must only use them as authorised and within legal limits to avoid health risks and enforcement.
Food additives are substances added to food for a specific technological purpose during manufacture, processing or storage. They include:
Additives must be authorised for use in particular foods and used within legal limits. Once authorised, additives are given E numbers, which are used in the UK, EU and associated countries to show that they have passed safety checks for particular uses.
If you use food additives, you must:
Under the Windsor Framework, Northern Ireland continues to apply EU food additives law. A list of approved additives is included in Regulation 1333/2008. You can search the Food and Feed Information Portal Database to see the list of additives approved for use in food in the EU and their conditions of use.
Great Britain has its own but closely aligned GB regime for food additives. There is some flexibility for GB-approved additives used in eligible goods moved under the Northern Ireland retail movement scheme.
If you use additives in your food and drink products, you must:
Extra labelling rules apply to some additives. For example:
These warnings are especially important for people with conditions such as phenylketonuria (PKU).
Food colours are additives used to change or strengthen the colour of food and drink. They are used to make products look consistent and more appealing. For example, colour additives can:
Only approved food colours can be used in food across the EU and the UK. Unauthorised substances, including industrial dyes like Sudan dyes, butter yellow or toluidine red, are prohibited due to a lack of safety assessments.
Approved food colours can be used in both commercial and domestic food preparation. They can be either natural or synthetic (artificial).
If you use food colours, you must:
Check out the full list of permitted food colours in the EU.
Research has suggested a link between consuming certain food colours and hyperactivity in children. These colours include:
If you use any of these colours in food or drink products (except alcoholic drinks above 1.2% ABV), you must include a warning label on the packaging that says: 'May have an adverse effect on activity and attention in children'. You should also check if your suppliers - including those overseas - use these colours to ensure proper labelling.
If you use any of these additives, the FSA suggests that you consider reformulating or using alternatives, especially if your products are aimed at children.
Restrictions on the type of packaging and food contact materials that can be used for food products, and how to check your packaging is safe and compliant.
Food contact materials (FCMs) are materials and articles that are intended to, or can be reasonably expected to, come into contact with food during its production, processing, storage, preparation and serving.
This includes direct or indirect contact through things like:
FCMs can be made from a range of materials including plastic, rubber, paper, ceramic, and metal. Chemicals can migrate from these materials into food and drink. The law aims to make sure chemical migration does not pose a risk to human health, or change the taste, smell, nature or quality of the food.
To ensure food safety, all FCMs must comply with relevant regulations. Northern Ireland businesses must follow EU rules on food contact materials under the Windsor Framework.
All FCMs must meet Regulation (EC) No 1935/2004, which sets general safety standards for food contact materials. All FCMs must also follow good manufacturing practices under Regulation (EC) No 2023/2006. In addition to the general legislation, certain FCMs - ceramic materials, regenerated cellulose film, plastics (including recycled plastic), and active and intelligent materials - are covered by specific EU measures. For materials without specific measures like paper, glass, wood, metals, textiles or inks, general safety rules apply.
In Northern Ireland, the Materials and Articles in Contact with Food Regulations (Northern Ireland) 2012 enforce the EU regulations directly. New or novel substances or processes in FCMs must follow the EU authorisation process.
Great Britain uses assimilated versions of the same regulations and has its own FCM authorisation process, but NI remains fully aligned with EU law. Pre-packaged FCMs authorised in Great Britain can enter Northern Ireland retail via the NI retail movement scheme (NIRMS) with 'Not for EU' labelling.
If you manufacture, import, process, distribute or use FCMs in food production, processing or packaging, you should:
FCMs must be labelled to show they are suitable for food use, unless the purpose is obvious, such as with a knife or plate. Labels must contain the glass and fork symbol or the words 'for food contact'. Include any necessary instructions, for example on maximum temperature or suitable food types like 'not for fatty foods'. You should check supplier DoCs to confirm labelling meets the relevant rules.
In Northern Ireland, local councils enforce legislation within the Food Standards Agency's (FSA) remit on food contact materials. They do this through inspections, sampling and document checks. If you do not comply, you may get an improvement notice, have products seized or face prosecution. Contact your local council for advice.
The FSA acts as the competent authority in Northern Ireland for handling EU applications and notifications under Commission Regulation 2022/1616 for new or novel recycled plastic processes used in food contact materials. All other FCMs follow direct EU processes under the Windsor Framework.
Rules on using irradiated food in your business and how the law regulates this process and labelling.
Food irradiation is the treatment of food with ionising radiation. Only certain food categories may be irradiated. The treatment involves exposing food to electron beams, X-rays or gamma rays. It must be carried out at approved facilities and under strict controls. Irradiated foods must be clearly labelled as 'irradiated' or 'treated with ionising radiation'.
Food irradiation can be used to:
The law states irradiation can only be used if it benefits consumers. Businesses that want to irradiate a food product have to be able to show that the benefits of irradiation outweigh any negatives.
The UK law allows seven categories of foods to be irradiated:
See also the scope of foods and food ingredients authorised for irradiation in the EU.
Major international bodies (including the World Health Organisation, UN Food and Agriculture Organisation and European scientific committees) consider irradiation safe when used within legal limits. The UK Food Standards Agency (FSA) also recognises irradiation of food as a safe processing technique and oversees irradiated food regulation across the UK.
If you use or sell irradiated food, you must:
If irradiated food is used as an ingredient, these words must appear next to the ingredient in the ingredients list. If irradiated food is not pre-packed, these words must appear on a display or notice above or beside the container.
Regulators can detect whether foods have been irradiated and sample foods on the market to check that the rules are followed. They can also check that the products are correctly labelled.
How acrylamide forms in food, how it affects health, and practical steps to reduce levels of acrylamide in food products.
Acrylamide is a chemical that can form when you cook carbohydrate-rich (starchy) foods at high temperatures (above 120°C). It is mainly found in:
Acrylamide is also present in tobacco smoke and coffee (from roasting), and in low levels in some dried fruits like prunes or pears due to processing heat, but is not typically present in raw foods.
Acrylamide is a natural by-product that forms during frying, baking, roasting, grilling and toasting of starchy food, usually at temperatures above 120°C. It is a product of the Maillard reaction where the amino acid asparagine reacts with reducing sugars during browning. This reaction produces the desirable flavour, crispness and colour in food, but can also generate acrylamide. Boiling and steaming do not usually lead to the formation of acrylamide.
Laboratory tests show that acrylamide in the diet causes cancer in animals. Scientists agree that acrylamide in food has the potential to cause cancer in humans as well. The Food Standards Agency (FSA) recommends that the amount of acrylamide we all consume is reduced, as a precaution. See more information on the risks of acrylamide in foods.
If you operate a food business, you must put in place practical steps to manage acrylamide as part of your food safety management system, and keep levels as low as possible. You are expected to:
Different requirements will apply depending on the nature and size of the business. Some common mitigation steps may involve:
There are currently no regulatory safe limits set for acrylamide in food, only mitigation measures and benchmark levels under Regulation (EU) 2017/2158 (for Northern Ireland) to guide performance. However, food contact materials rules limit acrylamide migration from plastic into food to 0.01 mg/kg (not detectable at that level).
Check the FSA enforcement guidelines, UK industry guides and the FoodDrinkEurope acrylamide toolkit for more details.
How residues of pesticides and veterinary medicines in food are controlled and what food businesses must do to ensure compliance.
Chemical residues are traces of pesticides (used on crops) or veterinary medicines (used on food-producing animals) that can remain in food. They may be found in fruit, vegetables, cereals, meat, milk, eggs and other animal products.
Food businesses are responsible for ensuring that the food they produce or import is compliant with current legislation, including rules on specified maximum residue levels.
MRLs are the maximum amounts of residue likely to remain in food when a product like a pesticide or veterinary medicine has been used correctly. They are set so that dietary intake remains within safe levels for consumers.
MRLs are expressed as milligrams of residue per kilogram of food product. Before being approved for use, pesticides and veterinary medicines must be proven to be completely safe for human consumption at their MRLs - and usually safe at much higher levels. National monitoring programmes regularly sample foods to check that residues are within legal limits. If residues above the MRL are found, authorities can investigate and take enforcement action.
Pesticides are used in agriculture, horticulture and domestic gardening to control pests, weeds and diseases. Small amounts of pesticides can remain in or on food as residues.
In the UK, the Health and Safety Executive (HSE) authorises which pesticides can be used and how. The Food Standards Agency (FSA) works closely with HSE on pesticides and food safety.
The Department for Environment, Food & Rural Affairs sets pesticide MRLs in Great Britain to make sure residues in food are not harmful to people.
In Northern Ireland, European Union MRLs apply to food or feed produced in or imported into and marketed within NI - this excludes goods moved from GB under the Northern Ireland retail movement scheme. See guidance on pesticide MRLs in Northern Ireland.
If you grow, import, process or sell food, you must:
Information on EU pesticide law and procedures is also available on the European Commission website. You can search for EU MRLs in the EU pesticides database.
Veterinary medicines are used to treat and prevent disease in animals, including animals used for food. Traces of these medicines can remain in meat, milk, eggs and other animal products.
In the UK, the Veterinary Medicines Directorate (VMD) assesses veterinary medicines before they are authorised. In Great Britain, VMD sets UK MRLs for veterinary medicines and ensures they are safe for consumers. In Northern Ireland, EU MRLs for veterinary medicines apply under EU law.
The FSA assesses any food safety risks from residues in food, and enforcement in Northern Ireland is carried out by the relevant NI authorities, including the Department of Agriculture, Environment and Rural Affairs, under the veterinary medicines and food law frameworks.
If you keep food‑producing animals, you must:
If you buy animal products for processing or retail, you should:
Residue monitoring programmes run nationally. If residues exceed MRLs, national agencies and enforcement bodies can investigate farms or supply chains to identify and resolve the issue.
What counts as a novel food, why businesses develop them, and how novel foods are regulated in Northern Ireland and the UK.
Novel foods are foods that have not been consumed to a significant degree in the European Union before 15 May 1997. This includes foods with no history of consumption and foods produced using new processes that change the product.
A food, ingredient or process may be novel if it:
Examples of novel foods include:
Examples of novel food technology and processes include:
Food businesses may develop novel foods because they:
If you are considering a new ingredient or process, you must be aware of the rules around novel food regulation and authorisation.
Which products are covered by novel food regulation, which are exempt, and how novel food rules apply in Northern Ireland and Great Britain.
Novel foods regulation controls which new foods and food processes can be placed on the market. A food is novel if it was not sold to a significant degree in the European Union before 15 May 1997.
The novel foods regulation applies to:
Engineered nanomaterials, certain animal‑derived foods (for example, cultured meat and some insect products), and some new forms of vitamins and minerals are also treated as novel foods under the same regulation.
The regulation requires that novel foods be safe for consumers and properly labelled, so as not to mislead consumers. If novel food is intended to replace another food, it must not differ in a way that the consumption of the novel food would be nutritionally disadvantageous for the consumer
If a food or ingredient has a proven history of safe use as food and was sold commercially in at least one EU member state before 15 May 1997, it is generally not considered a novel food.
In Northern Ireland, EU Regulation (EU) 2015/2283 on novel foods continues to apply. The Novel Foods Regulations (Northern Ireland) 2017 sets out how the EU rules are applied and enforced. Authorisations are granted at the EU level and listed on the Union list of authorised novel foods.
In Great Britain, novel foods are authorised under the GB regime. Businesses apply through the UK-regulated products application service. Some GB-authorised products may be supplied into NI via the Northern Ireland retail movement scheme, subject to scheme conditions.
It is your responsibility to know if the novel foods regulation applies to a product you want to sell. If you are not sure whether a food or ingredient is considered novel in Northern Ireland, you should:
For GB authorisation, look at the Food Standards Agency (FSA) guidance to understand how novel products are classified and assessed.
If you remain unsure regarding the novel food status of your product, you should follow the procedure for the determination of novel food status, and contact the competent authority of the Member State where you first intend to place your product on the market.
Food business operators must provide the necessary information to the Member State to enable it to determine whether or not a food falls within the scope of the regulation. Before you can place novel foods on the market, they must undergo safety assessment and authorisation.
Understand different authorisation routes for novel foods, and how to get authorisation for novel food in Northern Ireland, Great Britain and Europe.
Novel food law requires all novel foods to undergo a formal safety assessment and authorisation before they can be placed on the market. There are two main routes for the authorisation of novel foods under the regulation that applies in Northern Ireland and Europe.
This is a simplified route for foods that are new to the EU or NI, based on a documented history of their safe use in their country of origin. Businesses apply through an online notification to the European Commission. This route has reduced dossier requirements and a shorter assessment process than for other novel foods. Read the European Food Safety Authority (EFSA) guidance on the authorisation of traditional foods from third countries.
For all non-traditional novel foods, you must submit a full application to the European Commission through their e-submission food chain platform. For your application, you must prepare a detailed dossier describing the food, production, uses, consumers and safety rationale. Once the Commission has validated the application, they will ask EFSA to carry out a scientific safety assessment.
The safety assessment for a full application normally covers:
If the assessment is favourable, the product will be added to the Union list of authorised novel foods and can be lawfully marketed in the EU subject to any conditions of use.
If you want to market a novel food in NI that is not yet authorised in the EU, read the full guidance on procedures to request a novel food authorisation.
In Great Britain, novel foods are authorised under the UK-regulated products framework, using the Food Standards Agency (FSA) risk assessment. Businesses apply for authorisation through the UK-regulated products application service. GB also maintains its own list of authorised regulated food and feed products.
If you plan to sell in both Great Britain and Northern Ireland/EU, you will need to be aware of the relevant Windsor Framework or Unfettered Market Access requirements.
For GB products moving into NI, you may need both GB and EU novel food authorisations, unless the goods are moving under the Northern Ireland Retail Movement Scheme (NIRMS). Under the Windsor Framework, some GB-authorised pre-packed retail products may be supplied into Northern Ireland via the NIRMS, subject to scheme conditions and product scope.
Novel foods produced in Northern Ireland must follow EU Regulation (EU) 2015/2283, however can be placed onto the GB market, provided they are Qualifying Northern Ireland Goods.
If you place products directly on the Northern Ireland market, you must comply with EU novel foods rules and ensure the product is on the EU Union list, unless the product is moved under NIRMS. If you develop or import a new product, you may need:
Read more about novel food regulation that applies in NI and GB and keep up to date with the FSA’s guidance on novel food authorisation.
An explanation of nanotechnology and cloning in food industry, and how these technologies are regulated when used in the production of food and food products.
Nanotechnology and animal cloning are emerging technologies that can affect the food chain and may therefore fall under the novel food regulation, requiring safety assessments and authorisation before they can be placed on the market.
Engineered nanotechnology is a developing science. It is the manufacture and use of materials and structures in very small sizes, measured using the 'nanometre scale'. A nanometre is one-millionth of a millimetre. Because very small particles can behave differently from larger forms of the same substance, applications in the food and feed chain involving engineered nanomaterials are subject to specific risk assessments.
Nanomaterials can be used in foods, food supplements, food contact materials and animal feed. Their purpose can vary. For example, they can be used to change texture, improve stability and shelf-life, or deliver nutrients.
Under the EU novel food regulation, any food that consists of, contains, or uses engineered nanomaterials as an ingredient is treated as a novel food and must be authorised and safety-tested before it can be marketed in the Northern Ireland and European Union. Great Britain follows a similar, but separate, regulated food framework. Read more on novel food regulation.
If you intend to use nanotechnology in a food, feed or food contact material, you must check if the material is already authorised for use and if the nanoform is covered. Where a nanoform is not already authorised, you will need to apply for novel food authorisation, providing detailed characterisation of the nanomaterial and data on exposure, toxicology and any nanospecific hazards in line with relevant safety guidance.
Nanomaterials can also be regulated under other regimes without always coming through the novel food route, depending on how they are used. These regimes could be related to:
The European Food Safety Authority (EFSA) is responsible for the risk assessment of the use of nanomaterials in food and feed placed in the EU and Northern Ireland market. The Food Standards Agency and other UK authorities control nanomaterials in food and feed in GB.
Under the Windsor Framework, certain GB‑approved foods (which could include products using nanomaterials) can move from GB to NI via the Northern Ireland Retail Movement Scheme (NIRMS), subject to scheme conditions.
Cloning is a reproductive technology used to produce genetically identical copies of animals. Scientific reviews have found no evidence that food from healthy animal clones is different from food from healthy conventionally bred animals, but there are ongoing concerns about the health and welfare of the cloned animals.
Cloning of farm animals is not currently used for commercial food production in the EU. If a business wanted to sell food from cloned animals on the EU market in future, any food from cloned animals would be treated as a novel food and could not be sold in the EU or Northern Ireland unless it had been safety assessed and authorised.
Cloning of farm animals is also subject to wider rules on food hygiene and on the protection of animals kept for farming purposes, which businesses would need to comply with if commercial cloning were ever introduced. EU institutions have debated stricter rules on cloning for many years, and a range of stakeholders still call for a broad ban on cloning for farming and on imports of food from cloned animals and their descendants.
This is an area businesses should keep under review, particularly livestock breeders, meat and dairy producers, importers of live animals or genetic material, and retailers sourcing animal products from outside the EU/UK.
Plant cloning is a long established, routine technique in agriculture and horticulture, and it is not regulated in the same way as animal cloning. The underlying legal framework is complex, but plant cloning is generally accepted and managed under standard plant health, seeds/propagating material and (where relevant) genetically modified organisms or plant‑breeding rules rather than any special cloning law.
What counts as a novel food, why businesses develop them, and how novel foods are regulated in Northern Ireland and the UK.
Novel foods are foods that have not been consumed to a significant degree in the European Union before 15 May 1997. This includes foods with no history of consumption and foods produced using new processes that change the product.
A food, ingredient or process may be novel if it:
Examples of novel foods include:
Examples of novel food technology and processes include:
Food businesses may develop novel foods because they:
If you are considering a new ingredient or process, you must be aware of the rules around novel food regulation and authorisation.
Which products are covered by novel food regulation, which are exempt, and how novel food rules apply in Northern Ireland and Great Britain.
Novel foods regulation controls which new foods and food processes can be placed on the market. A food is novel if it was not sold to a significant degree in the European Union before 15 May 1997.
The novel foods regulation applies to:
Engineered nanomaterials, certain animal‑derived foods (for example, cultured meat and some insect products), and some new forms of vitamins and minerals are also treated as novel foods under the same regulation.
The regulation requires that novel foods be safe for consumers and properly labelled, so as not to mislead consumers. If novel food is intended to replace another food, it must not differ in a way that the consumption of the novel food would be nutritionally disadvantageous for the consumer
If a food or ingredient has a proven history of safe use as food and was sold commercially in at least one EU member state before 15 May 1997, it is generally not considered a novel food.
In Northern Ireland, EU Regulation (EU) 2015/2283 on novel foods continues to apply. The Novel Foods Regulations (Northern Ireland) 2017 sets out how the EU rules are applied and enforced. Authorisations are granted at the EU level and listed on the Union list of authorised novel foods.
In Great Britain, novel foods are authorised under the GB regime. Businesses apply through the UK-regulated products application service. Some GB-authorised products may be supplied into NI via the Northern Ireland retail movement scheme, subject to scheme conditions.
It is your responsibility to know if the novel foods regulation applies to a product you want to sell. If you are not sure whether a food or ingredient is considered novel in Northern Ireland, you should:
For GB authorisation, look at the Food Standards Agency (FSA) guidance to understand how novel products are classified and assessed.
If you remain unsure regarding the novel food status of your product, you should follow the procedure for the determination of novel food status, and contact the competent authority of the Member State where you first intend to place your product on the market.
Food business operators must provide the necessary information to the Member State to enable it to determine whether or not a food falls within the scope of the regulation. Before you can place novel foods on the market, they must undergo safety assessment and authorisation.
Understand different authorisation routes for novel foods, and how to get authorisation for novel food in Northern Ireland, Great Britain and Europe.
Novel food law requires all novel foods to undergo a formal safety assessment and authorisation before they can be placed on the market. There are two main routes for the authorisation of novel foods under the regulation that applies in Northern Ireland and Europe.
This is a simplified route for foods that are new to the EU or NI, based on a documented history of their safe use in their country of origin. Businesses apply through an online notification to the European Commission. This route has reduced dossier requirements and a shorter assessment process than for other novel foods. Read the European Food Safety Authority (EFSA) guidance on the authorisation of traditional foods from third countries.
For all non-traditional novel foods, you must submit a full application to the European Commission through their e-submission food chain platform. For your application, you must prepare a detailed dossier describing the food, production, uses, consumers and safety rationale. Once the Commission has validated the application, they will ask EFSA to carry out a scientific safety assessment.
The safety assessment for a full application normally covers:
If the assessment is favourable, the product will be added to the Union list of authorised novel foods and can be lawfully marketed in the EU subject to any conditions of use.
If you want to market a novel food in NI that is not yet authorised in the EU, read the full guidance on procedures to request a novel food authorisation.
In Great Britain, novel foods are authorised under the UK-regulated products framework, using the Food Standards Agency (FSA) risk assessment. Businesses apply for authorisation through the UK-regulated products application service. GB also maintains its own list of authorised regulated food and feed products.
If you plan to sell in both Great Britain and Northern Ireland/EU, you will need to be aware of the relevant Windsor Framework or Unfettered Market Access requirements.
For GB products moving into NI, you may need both GB and EU novel food authorisations, unless the goods are moving under the Northern Ireland Retail Movement Scheme (NIRMS). Under the Windsor Framework, some GB-authorised pre-packed retail products may be supplied into Northern Ireland via the NIRMS, subject to scheme conditions and product scope.
Novel foods produced in Northern Ireland must follow EU Regulation (EU) 2015/2283, however can be placed onto the GB market, provided they are Qualifying Northern Ireland Goods.
If you place products directly on the Northern Ireland market, you must comply with EU novel foods rules and ensure the product is on the EU Union list, unless the product is moved under NIRMS. If you develop or import a new product, you may need:
Read more about novel food regulation that applies in NI and GB and keep up to date with the FSA’s guidance on novel food authorisation.
An explanation of nanotechnology and cloning in food industry, and how these technologies are regulated when used in the production of food and food products.
Nanotechnology and animal cloning are emerging technologies that can affect the food chain and may therefore fall under the novel food regulation, requiring safety assessments and authorisation before they can be placed on the market.
Engineered nanotechnology is a developing science. It is the manufacture and use of materials and structures in very small sizes, measured using the 'nanometre scale'. A nanometre is one-millionth of a millimetre. Because very small particles can behave differently from larger forms of the same substance, applications in the food and feed chain involving engineered nanomaterials are subject to specific risk assessments.
Nanomaterials can be used in foods, food supplements, food contact materials and animal feed. Their purpose can vary. For example, they can be used to change texture, improve stability and shelf-life, or deliver nutrients.
Under the EU novel food regulation, any food that consists of, contains, or uses engineered nanomaterials as an ingredient is treated as a novel food and must be authorised and safety-tested before it can be marketed in the Northern Ireland and European Union. Great Britain follows a similar, but separate, regulated food framework. Read more on novel food regulation.
If you intend to use nanotechnology in a food, feed or food contact material, you must check if the material is already authorised for use and if the nanoform is covered. Where a nanoform is not already authorised, you will need to apply for novel food authorisation, providing detailed characterisation of the nanomaterial and data on exposure, toxicology and any nanospecific hazards in line with relevant safety guidance.
Nanomaterials can also be regulated under other regimes without always coming through the novel food route, depending on how they are used. These regimes could be related to:
The European Food Safety Authority (EFSA) is responsible for the risk assessment of the use of nanomaterials in food and feed placed in the EU and Northern Ireland market. The Food Standards Agency and other UK authorities control nanomaterials in food and feed in GB.
Under the Windsor Framework, certain GB‑approved foods (which could include products using nanomaterials) can move from GB to NI via the Northern Ireland Retail Movement Scheme (NIRMS), subject to scheme conditions.
Cloning is a reproductive technology used to produce genetically identical copies of animals. Scientific reviews have found no evidence that food from healthy animal clones is different from food from healthy conventionally bred animals, but there are ongoing concerns about the health and welfare of the cloned animals.
Cloning of farm animals is not currently used for commercial food production in the EU. If a business wanted to sell food from cloned animals on the EU market in future, any food from cloned animals would be treated as a novel food and could not be sold in the EU or Northern Ireland unless it had been safety assessed and authorised.
Cloning of farm animals is also subject to wider rules on food hygiene and on the protection of animals kept for farming purposes, which businesses would need to comply with if commercial cloning were ever introduced. EU institutions have debated stricter rules on cloning for many years, and a range of stakeholders still call for a broad ban on cloning for farming and on imports of food from cloned animals and their descendants.
This is an area businesses should keep under review, particularly livestock breeders, meat and dairy producers, importers of live animals or genetic material, and retailers sourcing animal products from outside the EU/UK.
Plant cloning is a long established, routine technique in agriculture and horticulture, and it is not regulated in the same way as animal cloning. The underlying legal framework is complex, but plant cloning is generally accepted and managed under standard plant health, seeds/propagating material and (where relevant) genetically modified organisms or plant‑breeding rules rather than any special cloning law.
If you sell or supply food, you need to follow strict rules on using colours and additives in foodstuffs, including those linked to hyperactivity in children.
Colours and additives help make and preserve food and drink products, but you must only use them as authorised and within legal limits to avoid health risks and enforcement.
Food additives are substances added to food for a specific technological purpose during manufacture, processing or storage. They include:
Additives must be authorised for use in particular foods and used within legal limits. Once authorised, additives are given E numbers, which are used in the UK, EU and associated countries to show that they have passed safety checks for particular uses.
If you use food additives, you must:
Under the Windsor Framework, Northern Ireland continues to apply EU food additives law. A list of approved additives is included in Regulation 1333/2008. You can search the Food and Feed Information Portal Database to see the list of additives approved for use in food in the EU and their conditions of use.
Great Britain has its own but closely aligned GB regime for food additives. There is some flexibility for GB-approved additives used in eligible goods moved under the Northern Ireland retail movement scheme.
If you use additives in your food and drink products, you must:
Extra labelling rules apply to some additives. For example:
These warnings are especially important for people with conditions such as phenylketonuria (PKU).
Food colours are additives used to change or strengthen the colour of food and drink. They are used to make products look consistent and more appealing. For example, colour additives can:
Only approved food colours can be used in food across the EU and the UK. Unauthorised substances, including industrial dyes like Sudan dyes, butter yellow or toluidine red, are prohibited due to a lack of safety assessments.
Approved food colours can be used in both commercial and domestic food preparation. They can be either natural or synthetic (artificial).
If you use food colours, you must:
Check out the full list of permitted food colours in the EU.
Research has suggested a link between consuming certain food colours and hyperactivity in children. These colours include:
If you use any of these colours in food or drink products (except alcoholic drinks above 1.2% ABV), you must include a warning label on the packaging that says: 'May have an adverse effect on activity and attention in children'. You should also check if your suppliers - including those overseas - use these colours to ensure proper labelling.
If you use any of these additives, the FSA suggests that you consider reformulating or using alternatives, especially if your products are aimed at children.
Restrictions on the type of packaging and food contact materials that can be used for food products, and how to check your packaging is safe and compliant.
Food contact materials (FCMs) are materials and articles that are intended to, or can be reasonably expected to, come into contact with food during its production, processing, storage, preparation and serving.
This includes direct or indirect contact through things like:
FCMs can be made from a range of materials including plastic, rubber, paper, ceramic, and metal. Chemicals can migrate from these materials into food and drink. The law aims to make sure chemical migration does not pose a risk to human health, or change the taste, smell, nature or quality of the food.
To ensure food safety, all FCMs must comply with relevant regulations. Northern Ireland businesses must follow EU rules on food contact materials under the Windsor Framework.
All FCMs must meet Regulation (EC) No 1935/2004, which sets general safety standards for food contact materials. All FCMs must also follow good manufacturing practices under Regulation (EC) No 2023/2006. In addition to the general legislation, certain FCMs - ceramic materials, regenerated cellulose film, plastics (including recycled plastic), and active and intelligent materials - are covered by specific EU measures. For materials without specific measures like paper, glass, wood, metals, textiles or inks, general safety rules apply.
In Northern Ireland, the Materials and Articles in Contact with Food Regulations (Northern Ireland) 2012 enforce the EU regulations directly. New or novel substances or processes in FCMs must follow the EU authorisation process.
Great Britain uses assimilated versions of the same regulations and has its own FCM authorisation process, but NI remains fully aligned with EU law. Pre-packaged FCMs authorised in Great Britain can enter Northern Ireland retail via the NI retail movement scheme (NIRMS) with 'Not for EU' labelling.
If you manufacture, import, process, distribute or use FCMs in food production, processing or packaging, you should:
FCMs must be labelled to show they are suitable for food use, unless the purpose is obvious, such as with a knife or plate. Labels must contain the glass and fork symbol or the words 'for food contact'. Include any necessary instructions, for example on maximum temperature or suitable food types like 'not for fatty foods'. You should check supplier DoCs to confirm labelling meets the relevant rules.
In Northern Ireland, local councils enforce legislation within the Food Standards Agency's (FSA) remit on food contact materials. They do this through inspections, sampling and document checks. If you do not comply, you may get an improvement notice, have products seized or face prosecution. Contact your local council for advice.
The FSA acts as the competent authority in Northern Ireland for handling EU applications and notifications under Commission Regulation 2022/1616 for new or novel recycled plastic processes used in food contact materials. All other FCMs follow direct EU processes under the Windsor Framework.
Rules on using irradiated food in your business and how the law regulates this process and labelling.
Food irradiation is the treatment of food with ionising radiation. Only certain food categories may be irradiated. The treatment involves exposing food to electron beams, X-rays or gamma rays. It must be carried out at approved facilities and under strict controls. Irradiated foods must be clearly labelled as 'irradiated' or 'treated with ionising radiation'.
Food irradiation can be used to:
The law states irradiation can only be used if it benefits consumers. Businesses that want to irradiate a food product have to be able to show that the benefits of irradiation outweigh any negatives.
The UK law allows seven categories of foods to be irradiated:
See also the scope of foods and food ingredients authorised for irradiation in the EU.
Major international bodies (including the World Health Organisation, UN Food and Agriculture Organisation and European scientific committees) consider irradiation safe when used within legal limits. The UK Food Standards Agency (FSA) also recognises irradiation of food as a safe processing technique and oversees irradiated food regulation across the UK.
If you use or sell irradiated food, you must:
If irradiated food is used as an ingredient, these words must appear next to the ingredient in the ingredients list. If irradiated food is not pre-packed, these words must appear on a display or notice above or beside the container.
Regulators can detect whether foods have been irradiated and sample foods on the market to check that the rules are followed. They can also check that the products are correctly labelled.
How acrylamide forms in food, how it affects health, and practical steps to reduce levels of acrylamide in food products.
Acrylamide is a chemical that can form when you cook carbohydrate-rich (starchy) foods at high temperatures (above 120°C). It is mainly found in:
Acrylamide is also present in tobacco smoke and coffee (from roasting), and in low levels in some dried fruits like prunes or pears due to processing heat, but is not typically present in raw foods.
Acrylamide is a natural by-product that forms during frying, baking, roasting, grilling and toasting of starchy food, usually at temperatures above 120°C. It is a product of the Maillard reaction where the amino acid asparagine reacts with reducing sugars during browning. This reaction produces the desirable flavour, crispness and colour in food, but can also generate acrylamide. Boiling and steaming do not usually lead to the formation of acrylamide.
Laboratory tests show that acrylamide in the diet causes cancer in animals. Scientists agree that acrylamide in food has the potential to cause cancer in humans as well. The Food Standards Agency (FSA) recommends that the amount of acrylamide we all consume is reduced, as a precaution. See more information on the risks of acrylamide in foods.
If you operate a food business, you must put in place practical steps to manage acrylamide as part of your food safety management system, and keep levels as low as possible. You are expected to:
Different requirements will apply depending on the nature and size of the business. Some common mitigation steps may involve:
There are currently no regulatory safe limits set for acrylamide in food, only mitigation measures and benchmark levels under Regulation (EU) 2017/2158 (for Northern Ireland) to guide performance. However, food contact materials rules limit acrylamide migration from plastic into food to 0.01 mg/kg (not detectable at that level).
Check the FSA enforcement guidelines, UK industry guides and the FoodDrinkEurope acrylamide toolkit for more details.
How residues of pesticides and veterinary medicines in food are controlled and what food businesses must do to ensure compliance.
Chemical residues are traces of pesticides (used on crops) or veterinary medicines (used on food-producing animals) that can remain in food. They may be found in fruit, vegetables, cereals, meat, milk, eggs and other animal products.
Food businesses are responsible for ensuring that the food they produce or import is compliant with current legislation, including rules on specified maximum residue levels.
MRLs are the maximum amounts of residue likely to remain in food when a product like a pesticide or veterinary medicine has been used correctly. They are set so that dietary intake remains within safe levels for consumers.
MRLs are expressed as milligrams of residue per kilogram of food product. Before being approved for use, pesticides and veterinary medicines must be proven to be completely safe for human consumption at their MRLs - and usually safe at much higher levels. National monitoring programmes regularly sample foods to check that residues are within legal limits. If residues above the MRL are found, authorities can investigate and take enforcement action.
Pesticides are used in agriculture, horticulture and domestic gardening to control pests, weeds and diseases. Small amounts of pesticides can remain in or on food as residues.
In the UK, the Health and Safety Executive (HSE) authorises which pesticides can be used and how. The Food Standards Agency (FSA) works closely with HSE on pesticides and food safety.
The Department for Environment, Food & Rural Affairs sets pesticide MRLs in Great Britain to make sure residues in food are not harmful to people.
In Northern Ireland, European Union MRLs apply to food or feed produced in or imported into and marketed within NI - this excludes goods moved from GB under the Northern Ireland retail movement scheme. See guidance on pesticide MRLs in Northern Ireland.
If you grow, import, process or sell food, you must:
Information on EU pesticide law and procedures is also available on the European Commission website. You can search for EU MRLs in the EU pesticides database.
Veterinary medicines are used to treat and prevent disease in animals, including animals used for food. Traces of these medicines can remain in meat, milk, eggs and other animal products.
In the UK, the Veterinary Medicines Directorate (VMD) assesses veterinary medicines before they are authorised. In Great Britain, VMD sets UK MRLs for veterinary medicines and ensures they are safe for consumers. In Northern Ireland, EU MRLs for veterinary medicines apply under EU law.
The FSA assesses any food safety risks from residues in food, and enforcement in Northern Ireland is carried out by the relevant NI authorities, including the Department of Agriculture, Environment and Rural Affairs, under the veterinary medicines and food law frameworks.
If you keep food‑producing animals, you must:
If you buy animal products for processing or retail, you should:
Residue monitoring programmes run nationally. If residues exceed MRLs, national agencies and enforcement bodies can investigate farms or supply chains to identify and resolve the issue.
If you sell or supply food, you need to follow strict rules on using colours and additives in foodstuffs, including those linked to hyperactivity in children.
Colours and additives help make and preserve food and drink products, but you must only use them as authorised and within legal limits to avoid health risks and enforcement.
Food additives are substances added to food for a specific technological purpose during manufacture, processing or storage. They include:
Additives must be authorised for use in particular foods and used within legal limits. Once authorised, additives are given E numbers, which are used in the UK, EU and associated countries to show that they have passed safety checks for particular uses.
If you use food additives, you must:
Under the Windsor Framework, Northern Ireland continues to apply EU food additives law. A list of approved additives is included in Regulation 1333/2008. You can search the Food and Feed Information Portal Database to see the list of additives approved for use in food in the EU and their conditions of use.
Great Britain has its own but closely aligned GB regime for food additives. There is some flexibility for GB-approved additives used in eligible goods moved under the Northern Ireland retail movement scheme.
If you use additives in your food and drink products, you must:
Extra labelling rules apply to some additives. For example:
These warnings are especially important for people with conditions such as phenylketonuria (PKU).
Food colours are additives used to change or strengthen the colour of food and drink. They are used to make products look consistent and more appealing. For example, colour additives can:
Only approved food colours can be used in food across the EU and the UK. Unauthorised substances, including industrial dyes like Sudan dyes, butter yellow or toluidine red, are prohibited due to a lack of safety assessments.
Approved food colours can be used in both commercial and domestic food preparation. They can be either natural or synthetic (artificial).
If you use food colours, you must:
Check out the full list of permitted food colours in the EU.
Research has suggested a link between consuming certain food colours and hyperactivity in children. These colours include:
If you use any of these colours in food or drink products (except alcoholic drinks above 1.2% ABV), you must include a warning label on the packaging that says: 'May have an adverse effect on activity and attention in children'. You should also check if your suppliers - including those overseas - use these colours to ensure proper labelling.
If you use any of these additives, the FSA suggests that you consider reformulating or using alternatives, especially if your products are aimed at children.
Restrictions on the type of packaging and food contact materials that can be used for food products, and how to check your packaging is safe and compliant.
Food contact materials (FCMs) are materials and articles that are intended to, or can be reasonably expected to, come into contact with food during its production, processing, storage, preparation and serving.
This includes direct or indirect contact through things like:
FCMs can be made from a range of materials including plastic, rubber, paper, ceramic, and metal. Chemicals can migrate from these materials into food and drink. The law aims to make sure chemical migration does not pose a risk to human health, or change the taste, smell, nature or quality of the food.
To ensure food safety, all FCMs must comply with relevant regulations. Northern Ireland businesses must follow EU rules on food contact materials under the Windsor Framework.
All FCMs must meet Regulation (EC) No 1935/2004, which sets general safety standards for food contact materials. All FCMs must also follow good manufacturing practices under Regulation (EC) No 2023/2006. In addition to the general legislation, certain FCMs - ceramic materials, regenerated cellulose film, plastics (including recycled plastic), and active and intelligent materials - are covered by specific EU measures. For materials without specific measures like paper, glass, wood, metals, textiles or inks, general safety rules apply.
In Northern Ireland, the Materials and Articles in Contact with Food Regulations (Northern Ireland) 2012 enforce the EU regulations directly. New or novel substances or processes in FCMs must follow the EU authorisation process.
Great Britain uses assimilated versions of the same regulations and has its own FCM authorisation process, but NI remains fully aligned with EU law. Pre-packaged FCMs authorised in Great Britain can enter Northern Ireland retail via the NI retail movement scheme (NIRMS) with 'Not for EU' labelling.
If you manufacture, import, process, distribute or use FCMs in food production, processing or packaging, you should:
FCMs must be labelled to show they are suitable for food use, unless the purpose is obvious, such as with a knife or plate. Labels must contain the glass and fork symbol or the words 'for food contact'. Include any necessary instructions, for example on maximum temperature or suitable food types like 'not for fatty foods'. You should check supplier DoCs to confirm labelling meets the relevant rules.
In Northern Ireland, local councils enforce legislation within the Food Standards Agency's (FSA) remit on food contact materials. They do this through inspections, sampling and document checks. If you do not comply, you may get an improvement notice, have products seized or face prosecution. Contact your local council for advice.
The FSA acts as the competent authority in Northern Ireland for handling EU applications and notifications under Commission Regulation 2022/1616 for new or novel recycled plastic processes used in food contact materials. All other FCMs follow direct EU processes under the Windsor Framework.
Rules on using irradiated food in your business and how the law regulates this process and labelling.
Food irradiation is the treatment of food with ionising radiation. Only certain food categories may be irradiated. The treatment involves exposing food to electron beams, X-rays or gamma rays. It must be carried out at approved facilities and under strict controls. Irradiated foods must be clearly labelled as 'irradiated' or 'treated with ionising radiation'.
Food irradiation can be used to:
The law states irradiation can only be used if it benefits consumers. Businesses that want to irradiate a food product have to be able to show that the benefits of irradiation outweigh any negatives.
The UK law allows seven categories of foods to be irradiated:
See also the scope of foods and food ingredients authorised for irradiation in the EU.
Major international bodies (including the World Health Organisation, UN Food and Agriculture Organisation and European scientific committees) consider irradiation safe when used within legal limits. The UK Food Standards Agency (FSA) also recognises irradiation of food as a safe processing technique and oversees irradiated food regulation across the UK.
If you use or sell irradiated food, you must:
If irradiated food is used as an ingredient, these words must appear next to the ingredient in the ingredients list. If irradiated food is not pre-packed, these words must appear on a display or notice above or beside the container.
Regulators can detect whether foods have been irradiated and sample foods on the market to check that the rules are followed. They can also check that the products are correctly labelled.
How acrylamide forms in food, how it affects health, and practical steps to reduce levels of acrylamide in food products.
Acrylamide is a chemical that can form when you cook carbohydrate-rich (starchy) foods at high temperatures (above 120°C). It is mainly found in:
Acrylamide is also present in tobacco smoke and coffee (from roasting), and in low levels in some dried fruits like prunes or pears due to processing heat, but is not typically present in raw foods.
Acrylamide is a natural by-product that forms during frying, baking, roasting, grilling and toasting of starchy food, usually at temperatures above 120°C. It is a product of the Maillard reaction where the amino acid asparagine reacts with reducing sugars during browning. This reaction produces the desirable flavour, crispness and colour in food, but can also generate acrylamide. Boiling and steaming do not usually lead to the formation of acrylamide.
Laboratory tests show that acrylamide in the diet causes cancer in animals. Scientists agree that acrylamide in food has the potential to cause cancer in humans as well. The Food Standards Agency (FSA) recommends that the amount of acrylamide we all consume is reduced, as a precaution. See more information on the risks of acrylamide in foods.
If you operate a food business, you must put in place practical steps to manage acrylamide as part of your food safety management system, and keep levels as low as possible. You are expected to:
Different requirements will apply depending on the nature and size of the business. Some common mitigation steps may involve:
There are currently no regulatory safe limits set for acrylamide in food, only mitigation measures and benchmark levels under Regulation (EU) 2017/2158 (for Northern Ireland) to guide performance. However, food contact materials rules limit acrylamide migration from plastic into food to 0.01 mg/kg (not detectable at that level).
Check the FSA enforcement guidelines, UK industry guides and the FoodDrinkEurope acrylamide toolkit for more details.
How residues of pesticides and veterinary medicines in food are controlled and what food businesses must do to ensure compliance.
Chemical residues are traces of pesticides (used on crops) or veterinary medicines (used on food-producing animals) that can remain in food. They may be found in fruit, vegetables, cereals, meat, milk, eggs and other animal products.
Food businesses are responsible for ensuring that the food they produce or import is compliant with current legislation, including rules on specified maximum residue levels.
MRLs are the maximum amounts of residue likely to remain in food when a product like a pesticide or veterinary medicine has been used correctly. They are set so that dietary intake remains within safe levels for consumers.
MRLs are expressed as milligrams of residue per kilogram of food product. Before being approved for use, pesticides and veterinary medicines must be proven to be completely safe for human consumption at their MRLs - and usually safe at much higher levels. National monitoring programmes regularly sample foods to check that residues are within legal limits. If residues above the MRL are found, authorities can investigate and take enforcement action.
Pesticides are used in agriculture, horticulture and domestic gardening to control pests, weeds and diseases. Small amounts of pesticides can remain in or on food as residues.
In the UK, the Health and Safety Executive (HSE) authorises which pesticides can be used and how. The Food Standards Agency (FSA) works closely with HSE on pesticides and food safety.
The Department for Environment, Food & Rural Affairs sets pesticide MRLs in Great Britain to make sure residues in food are not harmful to people.
In Northern Ireland, European Union MRLs apply to food or feed produced in or imported into and marketed within NI - this excludes goods moved from GB under the Northern Ireland retail movement scheme. See guidance on pesticide MRLs in Northern Ireland.
If you grow, import, process or sell food, you must:
Information on EU pesticide law and procedures is also available on the European Commission website. You can search for EU MRLs in the EU pesticides database.
Veterinary medicines are used to treat and prevent disease in animals, including animals used for food. Traces of these medicines can remain in meat, milk, eggs and other animal products.
In the UK, the Veterinary Medicines Directorate (VMD) assesses veterinary medicines before they are authorised. In Great Britain, VMD sets UK MRLs for veterinary medicines and ensures they are safe for consumers. In Northern Ireland, EU MRLs for veterinary medicines apply under EU law.
The FSA assesses any food safety risks from residues in food, and enforcement in Northern Ireland is carried out by the relevant NI authorities, including the Department of Agriculture, Environment and Rural Affairs, under the veterinary medicines and food law frameworks.
If you keep food‑producing animals, you must:
If you buy animal products for processing or retail, you should:
Residue monitoring programmes run nationally. If residues exceed MRLs, national agencies and enforcement bodies can investigate farms or supply chains to identify and resolve the issue.
If you sell or supply food, you need to follow strict rules on using colours and additives in foodstuffs, including those linked to hyperactivity in children.
Colours and additives help make and preserve food and drink products, but you must only use them as authorised and within legal limits to avoid health risks and enforcement.
Food additives are substances added to food for a specific technological purpose during manufacture, processing or storage. They include:
Additives must be authorised for use in particular foods and used within legal limits. Once authorised, additives are given E numbers, which are used in the UK, EU and associated countries to show that they have passed safety checks for particular uses.
If you use food additives, you must:
Under the Windsor Framework, Northern Ireland continues to apply EU food additives law. A list of approved additives is included in Regulation 1333/2008. You can search the Food and Feed Information Portal Database to see the list of additives approved for use in food in the EU and their conditions of use.
Great Britain has its own but closely aligned GB regime for food additives. There is some flexibility for GB-approved additives used in eligible goods moved under the Northern Ireland retail movement scheme.
If you use additives in your food and drink products, you must:
Extra labelling rules apply to some additives. For example:
These warnings are especially important for people with conditions such as phenylketonuria (PKU).
Food colours are additives used to change or strengthen the colour of food and drink. They are used to make products look consistent and more appealing. For example, colour additives can:
Only approved food colours can be used in food across the EU and the UK. Unauthorised substances, including industrial dyes like Sudan dyes, butter yellow or toluidine red, are prohibited due to a lack of safety assessments.
Approved food colours can be used in both commercial and domestic food preparation. They can be either natural or synthetic (artificial).
If you use food colours, you must:
Check out the full list of permitted food colours in the EU.
Research has suggested a link between consuming certain food colours and hyperactivity in children. These colours include:
If you use any of these colours in food or drink products (except alcoholic drinks above 1.2% ABV), you must include a warning label on the packaging that says: 'May have an adverse effect on activity and attention in children'. You should also check if your suppliers - including those overseas - use these colours to ensure proper labelling.
If you use any of these additives, the FSA suggests that you consider reformulating or using alternatives, especially if your products are aimed at children.
Restrictions on the type of packaging and food contact materials that can be used for food products, and how to check your packaging is safe and compliant.
Food contact materials (FCMs) are materials and articles that are intended to, or can be reasonably expected to, come into contact with food during its production, processing, storage, preparation and serving.
This includes direct or indirect contact through things like:
FCMs can be made from a range of materials including plastic, rubber, paper, ceramic, and metal. Chemicals can migrate from these materials into food and drink. The law aims to make sure chemical migration does not pose a risk to human health, or change the taste, smell, nature or quality of the food.
To ensure food safety, all FCMs must comply with relevant regulations. Northern Ireland businesses must follow EU rules on food contact materials under the Windsor Framework.
All FCMs must meet Regulation (EC) No 1935/2004, which sets general safety standards for food contact materials. All FCMs must also follow good manufacturing practices under Regulation (EC) No 2023/2006. In addition to the general legislation, certain FCMs - ceramic materials, regenerated cellulose film, plastics (including recycled plastic), and active and intelligent materials - are covered by specific EU measures. For materials without specific measures like paper, glass, wood, metals, textiles or inks, general safety rules apply.
In Northern Ireland, the Materials and Articles in Contact with Food Regulations (Northern Ireland) 2012 enforce the EU regulations directly. New or novel substances or processes in FCMs must follow the EU authorisation process.
Great Britain uses assimilated versions of the same regulations and has its own FCM authorisation process, but NI remains fully aligned with EU law. Pre-packaged FCMs authorised in Great Britain can enter Northern Ireland retail via the NI retail movement scheme (NIRMS) with 'Not for EU' labelling.
If you manufacture, import, process, distribute or use FCMs in food production, processing or packaging, you should:
FCMs must be labelled to show they are suitable for food use, unless the purpose is obvious, such as with a knife or plate. Labels must contain the glass and fork symbol or the words 'for food contact'. Include any necessary instructions, for example on maximum temperature or suitable food types like 'not for fatty foods'. You should check supplier DoCs to confirm labelling meets the relevant rules.
In Northern Ireland, local councils enforce legislation within the Food Standards Agency's (FSA) remit on food contact materials. They do this through inspections, sampling and document checks. If you do not comply, you may get an improvement notice, have products seized or face prosecution. Contact your local council for advice.
The FSA acts as the competent authority in Northern Ireland for handling EU applications and notifications under Commission Regulation 2022/1616 for new or novel recycled plastic processes used in food contact materials. All other FCMs follow direct EU processes under the Windsor Framework.
Rules on using irradiated food in your business and how the law regulates this process and labelling.
Food irradiation is the treatment of food with ionising radiation. Only certain food categories may be irradiated. The treatment involves exposing food to electron beams, X-rays or gamma rays. It must be carried out at approved facilities and under strict controls. Irradiated foods must be clearly labelled as 'irradiated' or 'treated with ionising radiation'.
Food irradiation can be used to:
The law states irradiation can only be used if it benefits consumers. Businesses that want to irradiate a food product have to be able to show that the benefits of irradiation outweigh any negatives.
The UK law allows seven categories of foods to be irradiated:
See also the scope of foods and food ingredients authorised for irradiation in the EU.
Major international bodies (including the World Health Organisation, UN Food and Agriculture Organisation and European scientific committees) consider irradiation safe when used within legal limits. The UK Food Standards Agency (FSA) also recognises irradiation of food as a safe processing technique and oversees irradiated food regulation across the UK.
If you use or sell irradiated food, you must:
If irradiated food is used as an ingredient, these words must appear next to the ingredient in the ingredients list. If irradiated food is not pre-packed, these words must appear on a display or notice above or beside the container.
Regulators can detect whether foods have been irradiated and sample foods on the market to check that the rules are followed. They can also check that the products are correctly labelled.
How acrylamide forms in food, how it affects health, and practical steps to reduce levels of acrylamide in food products.
Acrylamide is a chemical that can form when you cook carbohydrate-rich (starchy) foods at high temperatures (above 120°C). It is mainly found in:
Acrylamide is also present in tobacco smoke and coffee (from roasting), and in low levels in some dried fruits like prunes or pears due to processing heat, but is not typically present in raw foods.
Acrylamide is a natural by-product that forms during frying, baking, roasting, grilling and toasting of starchy food, usually at temperatures above 120°C. It is a product of the Maillard reaction where the amino acid asparagine reacts with reducing sugars during browning. This reaction produces the desirable flavour, crispness and colour in food, but can also generate acrylamide. Boiling and steaming do not usually lead to the formation of acrylamide.
Laboratory tests show that acrylamide in the diet causes cancer in animals. Scientists agree that acrylamide in food has the potential to cause cancer in humans as well. The Food Standards Agency (FSA) recommends that the amount of acrylamide we all consume is reduced, as a precaution. See more information on the risks of acrylamide in foods.
If you operate a food business, you must put in place practical steps to manage acrylamide as part of your food safety management system, and keep levels as low as possible. You are expected to:
Different requirements will apply depending on the nature and size of the business. Some common mitigation steps may involve:
There are currently no regulatory safe limits set for acrylamide in food, only mitigation measures and benchmark levels under Regulation (EU) 2017/2158 (for Northern Ireland) to guide performance. However, food contact materials rules limit acrylamide migration from plastic into food to 0.01 mg/kg (not detectable at that level).
Check the FSA enforcement guidelines, UK industry guides and the FoodDrinkEurope acrylamide toolkit for more details.
How residues of pesticides and veterinary medicines in food are controlled and what food businesses must do to ensure compliance.
Chemical residues are traces of pesticides (used on crops) or veterinary medicines (used on food-producing animals) that can remain in food. They may be found in fruit, vegetables, cereals, meat, milk, eggs and other animal products.
Food businesses are responsible for ensuring that the food they produce or import is compliant with current legislation, including rules on specified maximum residue levels.
MRLs are the maximum amounts of residue likely to remain in food when a product like a pesticide or veterinary medicine has been used correctly. They are set so that dietary intake remains within safe levels for consumers.
MRLs are expressed as milligrams of residue per kilogram of food product. Before being approved for use, pesticides and veterinary medicines must be proven to be completely safe for human consumption at their MRLs - and usually safe at much higher levels. National monitoring programmes regularly sample foods to check that residues are within legal limits. If residues above the MRL are found, authorities can investigate and take enforcement action.
Pesticides are used in agriculture, horticulture and domestic gardening to control pests, weeds and diseases. Small amounts of pesticides can remain in or on food as residues.
In the UK, the Health and Safety Executive (HSE) authorises which pesticides can be used and how. The Food Standards Agency (FSA) works closely with HSE on pesticides and food safety.
The Department for Environment, Food & Rural Affairs sets pesticide MRLs in Great Britain to make sure residues in food are not harmful to people.
In Northern Ireland, European Union MRLs apply to food or feed produced in or imported into and marketed within NI - this excludes goods moved from GB under the Northern Ireland retail movement scheme. See guidance on pesticide MRLs in Northern Ireland.
If you grow, import, process or sell food, you must:
Information on EU pesticide law and procedures is also available on the European Commission website. You can search for EU MRLs in the EU pesticides database.
Veterinary medicines are used to treat and prevent disease in animals, including animals used for food. Traces of these medicines can remain in meat, milk, eggs and other animal products.
In the UK, the Veterinary Medicines Directorate (VMD) assesses veterinary medicines before they are authorised. In Great Britain, VMD sets UK MRLs for veterinary medicines and ensures they are safe for consumers. In Northern Ireland, EU MRLs for veterinary medicines apply under EU law.
The FSA assesses any food safety risks from residues in food, and enforcement in Northern Ireland is carried out by the relevant NI authorities, including the Department of Agriculture, Environment and Rural Affairs, under the veterinary medicines and food law frameworks.
If you keep food‑producing animals, you must:
If you buy animal products for processing or retail, you should:
Residue monitoring programmes run nationally. If residues exceed MRLs, national agencies and enforcement bodies can investigate farms or supply chains to identify and resolve the issue.