Regulated products application guidance

We use some essential cookies to make this website work. We’d like to set additional cookies to understand how you use GOV.UK, remember your settings and improve government services. We also use cookies set by other sites to help us deliver content from their services. You have accepted additional cookies. You can change your cookie settings at any time. You have rejected additional cookies. You can change your cookie settings at any time. What you need to submit as part of your regulated product application. Added important information about the market authorisation process following the UK’s announcement on the UK-EU SPS Agreement to the top of the page (previously published on a duplicated version of this page). Contact details have been updated for SPS queries in the next steps section. Fixed broken links throughout. Fixed newsletter subscription link. Added information on SPS market reforms. The UK Government is negotiating a UK-EU Sanitary and Phytosanitary (SPS) Agreement with the European Union (EU) following the commitment made at the UK-EU Summit in May 2025 . This Agreement would create a common UK-EU SPS Zone. Businesses in the food and farming sectors and those associated with it, such as retailers and processors, may need to make some changes to follow EU rules, even if they only produce and sell within Great Britain (GB). While negotiations remain ongoing, all UK businesses large and small who grow, supply, process or transport agri-goods are encouraged to begin preparing for the changes ahead. You can read Defra’s information for businesses and sector specific guidance for further details. Subject to any exceptions negotiated, a UK-EU SPS Agreement based on dynamic alignment would mean: Due to the anticipated timeframe, a substantial number of applications in the GB Market Authorisation Service are unlikely to reach the point of ministerial decision before the Agreement is in place Exceptions to the dynamic alignment model may be negotiated in a limited number of areas, but these are subject to negotiations – further updates will be provided. Although the final scope of any agreement with the EU is yet to be agreed, the GOV.UK announcement indicates the EU legislation, and EU tertiary legislation (for example, delegated and implementing acts) currently in scope of the negotiations. The following website links can help with understanding EU food and feed safety legislation: We will continue to provide updates to all businesses with applications currently in the FSA / FSS Market Authorisation Service, and to relevant trade associations. Before you apply, you should: We will continue to monitor developments and provide updates when further information becomes available so that businesses can plan with confidence. For questions about applications or the market authorisation process: On 1 April 2025, the market authorisation process for regulated products was amended by legislation covering Great Britain (GB) which: Our guidance was amended to take these changes into account. You may wish to refer to further information on the reforms and how they relate to specific product types. Certain food and feed products, called regulated products, must go through a risk analysis process, and require market authorisation before they can be sold. Before you begin the application process, consider if you do need to apply for a regulated product market authorisation. This page explains the application requirements and will help you to work out if you need to make an application. You need to apply for a regulated product authorisation if you wish to place one of the following product types on the market in Great Britain (GB). Follow the links for specific FSA guidance according to each product type (‘regime’). These pages also link to the relevant guidance and regulations applicable to each regime: In addition, if you wish to apply for an authorisation of a cannabidiol (CBD) product, you can find more information in our CBD guida