Import animal by-products from the EU to Great Britain

Animal by-products (ABP) means ‘animal by-products and derived products not intended for human consumption’.

This guidance applies to businesses in Great Britain (England, Scotland and Wales) importing or moving animal by-products not intended for human consumption (ABP) from the EUEU. Imports from Iceland, Liechtenstein, Norway and NorthernSwitzerland Ireland. should also follow this guidance.

It also applies to goods imported for commercial purposes by post or courier. Contact your post or courier service to find out if they offer an import service for commercial imports and for more information about the process.

You need to follow different guidance if you’re importing: 

• high risk food and feed not of animalnon-animal origin (HRFNAO) 
• food and drink that are products of animal origin (POAO) 
• composite products 
• live animals and germinal products 
• live animals, including equines and animal products, from non-EU countries 

ABP is categorised into medium and low risk categories under the Border Target Operating Model (BTOM).

Unless they are from Ireland, all goods must enter Great Britain through a point of entry that has the relevant border control post (BCP).  

Goods moving directly from the Republic of Ireland must enter England or Scotland through a point of entry with a relevant BCP, or through Heysham. Goods from Ireland can enter Wales through any named point of entry. 

There are separate rules for qualifying Northern Ireland goods.

ABPs are also in category 1, 2 or 3. In most cases, you cannot import ABP from categories 1 or 2.

The BTOM risk categories do not correspond to ABP categories 1, 2 and 3.

Read more about importing ABP under the Border Target Operating Model.

Import ABP from approved businesses in the EU 

YouIn most cases, you can only import ABP from establishments approved by the EU to trade with the UK.

Notify

If you’re not sure whether you can import something from an establishment which has not been approved, email the Animal and Plant Health Agency (APHA) at imports@apha.gov.uk.

Transporting ABP

YouTransporters based in Great Britain must submitbe registered on Animal by-product operating plants: approved premises to transport ABP.

Transporters based in the EU must be registered on Establishments approved to export animals and animal products to Great Britain to transport ABP.

Check what documents you need

For medium risk imports, you need a health certificate if one is available. If there is no health certificate for your goods, you need a commercial document.

For low risk imports, you need a commercial document.

You no longer need a facilitation letter to import any ABP from the EU.

You do not need an import licence or authorisation for imports of ABP from the EU until 1 February 2025.

Health certificates

The EU exporter must apply for the GB health certificate in their own country. Competent authorities must use model health certificates to create versions that exporters can apply for.

If the exporter creates a GB health certificate using a system approved to produce verifiable PDF certificates, they do not need to send the original health certificate with the consignment. They must send you the official, verifiable PDF certificate once it has been signed by the competent authority. Use this for your import notification onin the import of products, animals, food and feed system (IPAFFS).

If the exporter does not use a system approved to notifyproduce verifiable PDF certificates, the Animalcompetent authority must send the original paper GB health certificate with the consignment and Plantsend Healthyou Agencyan (electronic copy to attach to your import notification in IPAFFS.

Commercial documents

The commercial document must be from the supplier and travel with your consignment. Suppliers can use the template commercial document for imports of ABP.

The commercial document must show a description of what’s in the consignment, including:

• quantity information in weight, volume or number of packages 
• whether it’s category 1, 2 or 3 material – if it’s a mixture it counts as the highest risk category, for example a mixture containing categories 1, 2 and 3 material would be treated as category 1 material 
• the animal species  

It must include the: 

• name of the person or organisation who sent it  
• name of the person or organisation it’s being sent to  
• premises of origin address and registration or approval number 
• date it left the premises of origin 
• destination premises address and registration or approval number 
• name, address and registration number of the transporter 

If the ABP is being transported in containers, it must also come with the container identification number. 

If the ABP is category 3 whole carcasses or heads destined for animal feed, the commercial document must also say the ear tag number of the animal if there was one.

If they are destined for uses other than animal feed, organic fertiliser or soil improver, the commercial document must contain information about processing for: 

• bones and bone products (except bone meal) 
• horn and horn products (except horn meal) 
• hooves and hoof products (except hoof meal) 

For beeswax destined for anything other than feeding farmed animals, the commercial document must say how it was refined or processed. 

For treated hides and skins, the commercial document must confirm that all precautions have been taken to avoid contamination with pathogenic agents. 

For game trophies or other products made only of hides or skin, the commercial document must say how they were processed and packaged. 

For treated feathers, parts of treated feathers and down, the commercial document must say how they were treated and washed. 

For display items, the commercial document must identify the authorisation of the competent authority of destination.

Notify APHA)

You must submit an import notification on IPAFFS to notify APHA about all imports of ABP subject to border controls from the EU. This is also known as a common health entry document (CHED).

You must do this at least one working day before the ABP is expected to arrive at the point of entry. 

You’ll get a notification reference number when you submit your import notification. The format of this number will be CHEDP.GB.YYYY.XXXXXXX.

Add information about the approved business you’re importing from

You need to add information to IPAFFS about the approved business you’re importing from, if the consignment is coming from: 

• the EU 
• Iceland
• Norway 
• Switzerland 
• Liechtenstein 
• San Marino 
• the Faroe Islands  
• Greenland

Follow these steps to add the approved business: 

1. Sign in or register to use IPAFFS. 
2. On the ‘Traders addresses’ page, select ‘Add a place of origin’, then select ‘Create a new place of origin’. 
3. In the ‘Place of origin name’ field, enter the full name of the exporting business, then its authorisation number. 
4. In the ‘Place of origin’ fields, enter the full address, telephone number, country and email address for the business. 
5. Save these details. Details will be saved to your address book so that you can use them again. 
6. Add the approved business to your notification.

If you need help with import notifications

YouIf canyou need technical help with IPAFFS, call APHA’s helpline on 03300 416 999 or email APHAServiceDesk@apha.gov.uk.

If you need help completing import notifications, contact the port health authority at the relevant BCP.

Confirm goods have arrived at their destination if they need channelling 

‘Channelling’ is where an ABP consignment must be moved directly from the point of entry to the approved point of destination. All precautions, including safe disposal of waste, must be taken to avoid risks of spreading diseases to animals or humans. 

The recipient must tell APHA within one day of the goods arriving at the destination. 

For low BTOM risk goods, the import risk summary table will tell you if your import needs channelling.  

The following medium BTOM risk ABPs are subject to channelling: 

• those intended for the manufacture of feed for fur animals, petfoodpet food other than raw petfood,pet food, and for derived products for uses other than for feeding farmed animals  
• rendered fats which are not destined for the production of feed for farmed animals, the manufacture of cosmetics, medicinal products or medical devices  
• fat derivatives 
• photogelatine 
• horns and horn products,products excluding(except horn meal,meal) and hooves and hoof products,products excluding(except hoof meal,meal) intended for the production of organic fertilizers or soil improvers  
• trade samples 

Untreated blood and blood products require channelling if all the following is true:

• they are for the manufacture of derived products for uses other than feeding farmed animals  
• they have been derived from animals belonging to the taxa Artiodactyla, Perissodactyla (excluding Equidae) and Proboscidea, including their crossbreeds 
• they come from a country or region where vaccination programmes against foot-and-mouth disease are being officially carried out and controlled in domestic ruminant animals for at least 12 months

Untreated blood products from animals other than Suidae, Tayassuidae and Equidae require channelling if they come from countries or regions where: 

• there have been recorded cases of vesicular stomatitis and bluetongue in the previous 12 months 
• vaccination programmes against vesicular stomatitis and bluetongue are being officially carried out against those diseases for at least 12 months in the susceptible animals 

Untreated blood products from Suidae and Tayassuidae animals require channelling if they come from countries or regions where: 

• no case of swine vesicular disease, classical swine fever and African swine fever has been recorded in the previous 12 months and vaccination has not been carried out against those diseases in those 12 months  
• cases of vesicular stomatitis (including the presence of seropositive animals) have been recorded in the previous12previous 12 months and vaccination has been carried out against this disease within those 12 months in the susceptible species

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