EUs Directive 2010/63/EU on the protection of animals used for scientific purposes
The EU has had specific legislation covering the use of animals for scientific purposes since 1986. On 22 September 2010 the EU adopted Directive 2010/63/EU which updates and replaces the 1986 Directive 86/609/EEC on the protection of animals used for scientific purposes. The Directive took full effect in the EU on 1 January 2013. The EU Commission maintains a comprehensive website about the Directive. Information about the numbers of animals used in research and testing is available here.
See also this more general page on Legislation.
When the Lisbon Treaty came into force in 2009, it introduced the recognition that animals are sentient beings, by amending the Treaty on the Functioning of the European Union (TFEU).
A description of the EU protection of farm animals (which are often used in research), and the concept of The Five Freedoms, is available here.
Directive 2010/63 was amended in 2019 by Regulation (EU) 2019/1010 (see Article 6 of the Regulation, which amends Articles 43 and 54 of the Directive, and deletes Article 57) to incorporate ambitious goals for reporting and transparency to help progress towards the ultimate goal of total replacement of animal use: Member States shall collect and make publicly available, on an annual basis, statistical information on the use of animals in procedures, including information on the actual severity of the procedures and on the origin and species of non-human primates used in procedures.
Norway implemented most of the Directive through national legislation on 1 July 2015 and then via the European Economic Area Agreement (EØS-avtalen) on 1 August 2016.
The Three Rs are implicitly mentioned in the Directive as an obligation for all those involved in the use of animals for scientific purposes.
The 2010/63 Directive includes a new definition of the categories of personnel who are involved in animal research. The functions are:
- a: those carrying out procedures on animals
- b: those designing procedures and projects
- c: those taking care of animals
- d: those killing animals
These functions must not be confused with the old FELASA categories A-D, which were very different.
The Directive includes the following Annexes:
- Annex I: List of animals referred to in Article 10 (animals bred for use in procedures)
- Annex II: List of non-human primates and dates referred to in the second subparagraph of Article 10(1)
- Annex III: Requirements for establishments and for the care and accommodation of animals*
- Annex IV: Methods of killing animals*
- Annex V: List of elements referred to in Article 23(3) (requirements for education, training and competence)
- Annex VI: Lists of elements referred to in Article 37(1)(c) (Non-Technical Project Summaries)
- Annex VII: Duties and tasks of the Union Reference Laboratory
- Annex VIII: Severity classification of procedures
'The aim of the new Directive is to strengthen legislation, and improve the welfare of those animals still needed to be used, as well as to firmly anchor the principle of the Three Rs, to Replace, Reduce and Refine the use of animals, in EU legislation.
The Directive is firmly based on the principle of the Three Rs, to replace, reduce and refine the use of animals used for scientific purposes.
The scope is now wider and includes foetuses of mammalian species in their last trimester of development and cephalopods, as well as animals used for the purposes of basic research, higher education and training.
It lays down minimum standards for housing and care, regulates the use of animals through a systematic project evaluation requiring inter alia assessment of pain, suffering distress and lasting harm caused to the animals.
It requires regular risk-based inspections and improves transparency through measures such as publication of non-technical project summaries and retrospective assessment.
The development, validation and implementation of alternative methods is promoted through measures such as establishment of a Union reference laboratory for the validation of alternative methods supported by laboratories within Member States and requiring Member States to promote alternative methods at national level.'
The text of the Directive and many resources about its use are available at:
This website includes sections on:
- Legislation and implementation
- The Three Rs and alternative approaches
- Statistics on the use of animals in experiments in the EU, including the ALURES statistical database for detailed datamining
- Opinions of EU Expert Committees on the use of animals in experiments
- Related topics within animal science and welfare
- Posters and guidance documents (see below for links to the individual guidance documents)
- Links, among others to the networks established under the Directive
The Commission has produced a glossary of terms to aid correct reporting.
The Member States have endorsed the following guidance documents:
- EU guidance document on animal welfare bodies and national committees
- EU guidance document on non-technical project summaries
- EU guidance document on inspections and enforcement
- EU guidance document on genetically altered animals
- EU guidance document on project evaluation and retrospective assessment
- EU guidance document on severity assessment framework
- EU guidance document on education and training framework
Commission Implementing Decision 2020/569/EU (16 April 2020) established a common format and information content for submissions from Member States in compliance with the Annexes in the Directive. This includes a template for the Non-Technical Project Summaries referred to in Article 43(1) and their updates, and the submission of statistical data. This Decision repealed an earlier Decision (2012/707/EU).
The journal Laboratory Animals has published ESLAV/ECLAM/LAVA/EVERI recommendations for the roles, responsibilities and training of the laboratory animal veterinarian and the designated veterinarian under Directive 2010/63/EU. These provide professional guidance on the role and postgraduate training of laboratory animal veterinarians, who may be working as designates veterinarians under the Directive.
A European Citizens Initiative (ECI) entitled Stop Vivisection to abrogate the Directive resulted in a public meeting, entitled Non-Animal Approaches - the Way Forward, for the stakeholders which was held in Brussels on 6-7 December 2016 (Conference Report). The Commission's response to the Initiative can be read here.
A new ECI, Save Cruelty Free Cosmetics, was registered in 2021 and validated in January 2023 (see the Eurogroup for animals website). It also includes petitions to commit to changes in the EU chemicals legislation and a legislative proposal plotting a roadmap to phase-out all animal testing in the EU before the end of the current legislative term.
Links to other relevant EU websites
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