Precursor chemical licensing
Licence and registration application information for companies that deal in precursor chemicals.
Overview
The effective control of chemicals used in the illicit manufacture of narcotic drugs and psychotropic substances is an important tool in combating drug trafficking. These chemicals, known as ‘drug precursors’, also have legitimate commercial uses as they are legally used in a wide variety of industrial processes and consumer products, such as medicines, flavourings and fragrances.
It is necessary to recognise and protect the legal trade in these substances, while at the same time discouraging their diversion for illicit purposes. Drug precursor chemicals should not be confused with Explosive precursor chemicals which are controlled under a separate regime.
This page is about applying for licences and registrations. For the requirements to document, record and label consignments of DPCs, please see this page.
Categories
Regulation of drug precursors covers a number of chemical substances which are divided into 4 categories:
- category 1 covers the most sensitive substances (the ‘main’ drug precursors)
- category 2 covers less sensitive substances and some pre-precursors
- category 3 covers bulk chemicals that can have different types of uses in the manufacturing process (for example, as feedstock, solvents or impurities removers)
- category 4 covers medicinal products of some category 1 substances
With the exception of category 4 drug precursor chemicals, the legislation generally excludes medicinal products for human use, but covers all natural products and preparations (or mixtures) containing at least one scheduled substance, provided that they can be extracted by ‘readily applicable or economically viable means’.
The precursors and chemicals frequently used in the illicit manufacture of narcotic drugs and psychotropic substances under control are defined by the United Nations International Control Board.
Read drug precursor chemicals: category and CN codes.
Legal background
The basis for precursor control is to be found in the United Nations Convention against Illicit Traffic in Narcotic Drugs and Psychotropic Substances adopted in Vienna on 19 December 1988.
UN convention
Article 12 of the convention specifically covers ‘substances frequently used in the illicit manufacture of narcotic drugs and psychotropic substances’ and requires that countries implement measures to control and monitor the legitimate trade in drug precursors as an essential way to prevent their diversion.
Legislation
The convention is implemented through the following legislation:
- Regulation (EC) No 273/2004 of the European Parliament and of the Council, on domestic use of drug precursor chemicals, as amended by The Law Enforcement and Security (Amendment) (EU Exit) Regulations 2019 and by The Controlled Drugs (Drug Precursors) (Amendment and Revocation) Regulations 2026. The relevant (similar) legislation in Northern Ireland
- Council Regulation (EC) No 111/2005 on international trade of drug precursor chemicals, as amended by The Law Enforcement and Security (Amendment) (EU Exit) Regulations 2019 and by The Controlled Drugs (Drug Precursors) (Amendment and Revocation) Regulations 2026. The relevant (similar) legislation in Northern Ireland
- Commission Delegated Regulation (EU) 2015/1011, which supplements the 2004 and 2005 Regulations, as amended by The Law Enforcement and Security (Amendment) (EU Exit) Regulations 2019 and by The Controlled Drugs (Drug Precursors) (Amendment and Revocation) Regulations 2026. The relevant (similar) legislation in Northern Ireland
- Commission Implementing Regulation (EU) 2015/1013, which lays down rules in respect of the 2004 and 2005 Regulations, as amended by The Law Enforcement and Security (Amendment) (EU Exit) Regulations 2019 and by The Controlled Drugs (Drug Precursors) (Amendment and Revocation) Regulations 2026. The relevant (similar) legislation in Northern Ireland
- The Controlled Drugs (Drug Precursors)(Intra-Community Trade) Regulations 2008 which specifies certain matters relating to the 2004 Regulation, as amended by The Law Enforcement and Security (Amendment) (EU Exit) Regulations 2019 and by The Controlled Drugs (Drug Precursors) (Amendment and Revocation) Regulations 2026
- The Controlled Drugs (Drug Precursors)(Community External Trade) Regulations 2008, which specifies certain matters relating to the 2005 Regulation, as amended by The Law Enforcement and Security (Amendment) (EU Exit) Regulations 2019 and by The Controlled Drugs (Drug Precursors) (Amendment and Revocation) Regulations 2026
- The Controlled Drugs (Drug Precursors) (Intra-Community Trade and Community External Trade) Regulations 2010, which details prescribed fees, as amended by The Controlled Drugs (Drug Precursors) (Amendment and Revocation) Regulations 2026
The two Regulations from 2008 specify who the ‘competent authorities’ are for each of the functions in the drug precursor chemicals legislation. These are the Secretary of State (i.e. the Home Secretary, encompassing both the Drugs and Firearms Licensing Unit and Border Force), the National Crime Agency, His Majesty’s Revenue and Customs and the police.
Definitions
The terms used in this guidance are defined as:
Placing on the market: any supply, whether in return for payment or free of charge, of scheduled substances; or the storage, manufacture, production, processing, trade, distribution or brokering of these substances for the purpose of supply.
Operator: any natural or legal person engaged in the placing on the market of scheduled substances.
Responsible officer: operators are required to appoint an officer responsible for the trade in scheduled substances. The officer shall be empowered to represent the operator and to ensure that the trade conducted takes place in compliance of regulations.
Guarantor: another senior person in the company that agrees to guarantee the responsible officer’s performance of their obligations.
Domestic licensing
Domestic licences are required for any companies that possess, manufacture, produce or supply drugs precursor chemicals in England, Wales or Scotland. Domestic licensing requirements apply to Category 1, 2 and 3 drug precursor chemicals.
Domestic licensing requirements for operators in precursors can be found on the Precursor chemicals wallchart for domestic licensing.
You must hold a valid domestic licence to be able to apply for an import-export licence.
Before you apply
To apply, you first need to register as a customer on the controlled drugs licensing system. After registering, you will receive a confirmation email from Drugs and Firearms Licensing (DFLU) containing a link that allows you to download your application form.
Your username and password will be automatically generated and sent to you in 2 separate emails.
Check your spam / junk folder if you do not receive these emails shortly after registering.
Your username and password will not give you immediate access to the web-based licensing portal. You will only get access if your application is successful.
You do not need to register again each time you apply.
If you have forgotten or lost your login details or need to reset your password, email dflu.dom@homeoffice.gov.uk. When contacting DFLU, use the following subject format: Password reset required - Company Name - Company Account Number.
Disclosure & Barring Service (DBS) Checks
If you have submitted a premises licence application, please be advised that your application will not be progressed until we are in receipt of DBS enhanced disclosure for all persons named on the application form.
For the purpose of a controlled drugs and precursor chemical licence DBS checks are undertaken by Matrix Security Watchdog, we do not accept any other DBS check. You can contact Matrix Security Watchdog directly on 01420 558 752 or visit their website https://www.matrixscreening.com/cheqs
Please note that the Disclosure and Barring Service offer an ‘update’ service whereby for new checks, individuals can opt to ‘subscribe’ to the update service on an annual basis. This will, in certain circumstances, enable a check to be potentially ‘portable’ and a subscription can only be bought within a limited time window. Should you opt for this then an email needs to be sent to us confirming that you provide us with explicit permission to obtain the information. You must provide your full name, DOB and disclosure date and reference number.
Please do not send a copy of your DBS certificate to DFLU unless requested to do so.
Apply for a domestic licence or registration
Before starting your application all prospective and existing licence holders should have the following information and documents ready:
- the company registration document from Companies House (if applicable)
- a valid Disclosure and Barring Service (completed via Security Watchdog) reference number and date of issue for the responsible officer and guarantor
- a certificate of good conduct for the responsible officer – this should be a brief letter signed by another officer of the company such as the guarantor and should, for example, confirm that the responsible officer is a fit and proper person to act as the responsible officer for precursor chemicals; they may also wish to state how long the responsible officer has worked for the company, the role they hold and a statement on how they have carried out their duties
- a purchase order (PO) number (if applicable to your company or organisation) for invoicing purposes
- knowledge of the PC substances and categories
Read the application guidance to help you complete your application.
Apply for a domestic licence to produce, supply or possess controlled drugs.
Existing licensees without a password should contact dflu.dom@homeoffice.gov.uk.
Domestic precursor licences and registrations specify the substances within the category which you are permitted to handle. If you need to amend these after a licence has been issued to you, you will need to submit an application for a further licence and a fee will be payable.
Fees
Our fees cover the costs of processing an application and are charged per licensing decision. The fee levels are set out in the The Controlled Drugs (Drug Precursors) (Intra-Community Trade and Community External Trade) Regulations 2010. Read the full list of fees for drugs precursor chemicals licences.
After you apply
Allow up to 16 weeks for us to contact you to arrange a compliance visit, if one is required.
Please note:
- all first time Category 1 (‘CAT 1’) licensees, new sites and upgrades require a licensing visit
- CAT 1 renewal applications will be visited every 1 to 5 years or more at our discretion; Category 2 and 3 registration renewals are not routinely visited, but can be on a risk assessed basis
- applications are only considered complete where all component parts of an application are correct and present
- if there is a delay because we have asked for more information regarding your application, it will take longer than 16 weeks to contact you to book a compliance visit
If your application is approved, you will receive an email with instructions for payment. We will not issue your licence until the fee is paid.
Once you have paid, the licence will be sent electronically by email.
Compliance visits
We may need to visit your company to check for compliance with controlled drugs regulations. We will only arrange a visit if everyone listed on the application has a valid DBS check.
Applications where a compliance visit is not needed
If you already hold a licence with us and we do not need to visit you, your application will be processed in 8 to 10 weeks from the point where an application acknowledgement email has been sent.
If we have asked for further information or documents, the 8 to 10 weeks will start at the point we have received all requested information and documents and the acknowledgement email has been sent.
You must confirm in writing if there have been any changes in the following areas since issuing your previous licence:
- security arrangements
- standard operating procedure relating to controlled drugs or precursor chemicals
- responsible persons or guarantor (if applicable)
The following information or documentation must be supplied:
- supporting photographs of your current storage arrangements, for example a photo of your safe open and closed, key safe or press as appropriate
- supporting photographs of a page from your register or records showing the most recent entries
- an electronic copy of your latest standard operating procedure (highlighting any amendments that have taken place)
End-user declarations
Regulations require that operators who supply category 1 substances are required to obtain a declaration from the end-user specifying the intended use of that substance.
Declarations relating to the supply of category 2 substances are dependent on the level of trade involved.
Import and export licensing
Import and export licences are required for companies for the movement of any drug precursor chemicals that are imported or exported to and from GB and, in some cases, Northern Ireland.
The import-export licensing requirements for trading in precursor chemicals can be found on the Precursor chemical export and import authorisation page. Please read the section on trade between Great Britain and Northern Ireland to ensure you are familiar with any changes to licensing requirements after 1 January 2021.
Before you apply
You need an NDS account to apply for an import or export licence. You can read the user guide for more information on what to do.
You will need a domestic licence covering the specific chemical for which you are applying before you can apply for an NDS account. If you do not have a valid domestic licence your request will be cancelled. Once your account is approved you will need to tell us about your overseas trading partners and details of your controlled drug preparations.
Please read the import and export section.
Fees
Read the full list of fees for drugs precursor chemicals licences.
All fees for import and export licences are invoiced in arrears at the end of the month. If fee invoices for import-export licences are not promptly settled we will not process further import-export licence applications until all outstanding invoices are paid.
Apply for an import or export licence
Import licences are valid for 3 months. Export licences are valid for either 2 months or in line with the permit of the importing country, whichever expires first. You need to apply for a new import or export licence for each individual shipment. Licences cannot be post-dated or retrospectively issued.
If you are applying for a UK export licence you must include a copy of the import permit or it will be rejected.
If you are applying for a Category 1 import licence you must upload a completed version of the and your domestic licence with your application or it will be rejected.
Pre-export notification (PEN): waiting period
The vast majority of export authorisation applications are subject to a pre-export notification (PEN) process. The proposed shipment is electronically notified between competent authorities by way of the pre-export notification (PEN) system; applicants need not apply separately for this.
This process takes up to 17 working days and a decision is reached regarding authorisation of the shipment after this process is completed. The competent authorities may refuse the import or export of the substance if there are grounds for suspecting that diversion might occur.
Please note this time is in addition to the standard DFLU import-export licencing processing time for applications not subject to the PEN process (up to 10 working days). You must therefore allow time for both the licence processing time and the PEN waiting period when planning your intended shipments.
Endorsements
A condition of all import and export licences issued by the Home Office is for an immediate online endorsement of the actual shipment amounts and date of shipment to be made on the NDS web portal, once they have been shipped.
If you do not regularly submit timely endorsements we will not process further licence applications from you.
Annual statistical returns
If you are a wholesaler, manufacturer, producer or supplier of controlled drugs or drug precursor chemicals you must send a completed annual returns form each year, to annualdrugreturns@homeoffice.gov.uk.
Read the guidance about annual statistical returns.
Trading in drug precursor chemicals between Great Britain and Northern Ireland
The United Kingdom left the European Union on 31 January 2020 and the subsequent transition period ended on 31 December 2020.
The Windsor Framework which was subsequently agreed by the EU and the UK affects the future trading relationship between Great Britain (GB) and Northern Ireland (NI) for drug precursor chemical control.
For the purposes of drug precursor chemical control, NI continues to apply European Union regulations, while GB does not. This means NI companies trading with European Union Member States will not require import or export licences as this is considered ‘intra-community trade’.
However, trade between GB and NI will be subject to licensing in accordance with the requirements in Precursor chemical export and import authorisation. This includes ‘category 4’ drug precursor chemicals, namely Medicinal Preparations of ephedrine and pseudoephedrine.
The Drug and Firearms Licensing Unit continues to act as one of the UK competent authorities for drug precursor chemical control. Both GB and NI companies should apply to the Drugs and Firearms Licensing Unit for their licences using the links above. No fee is charged for import and export licences between GB and NI.
Companies therefore need to submit an end-user declaration form to their supplier:
- customer declaration of specific uses of the scheduled category 1 or 2 substances (individual transactions)
- customer declaration of specific uses of the scheduled category 2 substances (multiple transactions)
Thefts and losses
You can report any theft or unaccounted losses of controlled drugs by email to dflu.dom@homeoffice.gov.uk using the thefts and losses form.
Licence no longer needed
If your company no longer needs a controlled drugs or precursor chemicals licence or registration you will need to submit a controlled drugs licence return premises closure statement.
Even if you continue to trade but no longer handle controlled drugs or precursor chemicals you will need to submit a statement. This includes site closures.
Documentation, records and labelling
There are also requirements to document, record and label consignments of DPCs.
Suspicious activity reports
If you notice any circumstances, such as unusual orders and transactions, which suggest that a drug precursor chemical being traded within the UK or between the UK and another country might be diverted to produce illicit drugs, you must notify the National Crime Agency immediately. This page tells you how to do that and what information you need to provide .
Personal information
You can read details of how we handle your personal information.
Contact details
Depending on your query, there are a number of ways to contact the DFLU.
Domestic licensing
Email dflu.dom@homeoffice.gov.uk
or call 0300 105 0248
This address deals with domestic (UK) controlled substance licences including precursor chemicals, applications, renewals, compliance visits, thefts and losses, surrender or returning licence, or general enquiries about domestic licensing.
Import and export licensing
Email dflu.ie@homeoffice.gov.uk
This address deals with the import and export of controlled substance into or from the UK, import and export licences, applications, endorsements of licences, or general enquiries about import and export licensing.
Customer complaints
Email dflu.complaints@homeoffice.gov.uk
This address deals with customer complaints about import and export, or domestic licensing of controlled drug, precursor chemical or industrial hemp licensing. You should first attempt to resolve any issues initially with either the domestic licensing or import-export team directly using the contact details above.
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