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Animals in Science Regulation Unit (ASRU) guidance and regulatory advice
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Recording and reporting the actual severity of regulated procedures
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- Guidance notes for project licence applications
From 5 July 2021, ASRU now provides regulatory delivery through 2 teams covering different areas each of which has a dedicated inbox. Read the Bridging ways of working guidance for advice.
Apply for licences
Three licences are required by the Animals (Scientific Procedures) Act 1986 (ASPA) before testing on animals is allowed. The 3 licences needed are:
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personal licence for each person carrying out procedures on animals
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project licence for the programme of work
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establishment licence for the place at which the work is carried out
You should use the Animals in Science Procedures e-Licensing (ASPeL) system for all personal and project licence applications.
Contact your establishments Home Office liaison contact/administrator to start your application online.
If you are from an establishment that is not yet licensed, email ASPELTechnicalQueries@homeoffice.gov.uk.
Before applying, please read the standard conditions for personal licences, project licences and establishment licences.
You can also read guidance on:
Add a named person role
People in named person roles are responsible for specific activities under the establishment licence (PEL), and you must add their names to the PEL in ASPeL. For example, the Named Animal Care and Welfare Officer (NACWO) oversees the care and welfare of animals.
Read about the requirements for named person roles in
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section 3.8 and section 8 in Guidance on the operation of ASPA.
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Guidance for training and continuous professional development under ASPA
When you add a named person to a PEL, this is classed as an amendment.
Find out how to nominate someone for a:
Any named person responsible for animal welfare on the PEL will need to complete aconflict of interest declaration form.
Prospective authority licensing requests
Animal studies carried out to meet regulatory requirements will be performed in compliance with UK and EU legislative bodies.
Where studies are performed for other regulatory bodies, for example the US, and the study requirements exceed the UK or EU regulatory requirements, you must submit a prospective authorisation request form to ASRU.
The project licence holder at the establishment should complete the