Describe and present which national and EU laws and guidance which regulate the scientific use of animals and in particular the activities of those carrying out scientific procedures involving them, as well as other forms of relevant animal welfare legislation, and discuss how to find the relevant legislation.
EU directive 2010/63/EU: authorizes animal experiments, mandates ethical review,
imposes requirements for the of use of animals, encourages the use of alternatives &
ensures the humane treatment and euthanasia of animals.
–> all EU members must follow these rules
National laws in Denmark
o Animal Experimentation Act
▪ overrules animal welfare act & governs the use of animals for
scientific purposes in Denmark.
▪ aligns with EU Directive to ensure high standards of animal welfare
▪ activities: ethical reviewing, compliance with 3Rs, sets standards for
care, housing & treatment & grants Animal Experiments
Inspectorate the authority to conduct inspections to ensure compliance
with regulations
o Animal Experimentation Oder gives more detailed descriptions of the rules
of the Animal Experimentation act
* Animal Experimentation Inspectorate gives licenses & monitors the compliance
with laws
* animal welfare bodies advices people on 3Rs, culture of care & legal requirements
* relevant legislations can be found on respective websites
This means, that all contries in the European Union have the same legislation, but in some individual contries they might be stricter in some ways, e.g., in the UK no animals can be used for educational purpose, in DK intensive suffering or intensive fear are not allowed in lab animals, and in Sweeden there is no lower limit.
Describe the authorisation that is needed before acting as user, breeder or supplier of laboratory animals and especially the authorisation required for projects and where applicable individuals. Describe who will grant you a license in Denmark, how this authority is organized, and which other functions this authority has.
Describe the roles and responsibilities of the local animal welfare bodies and the national committee for the protection of animals used for scientific purposes.
Local:
* focus on ensuring the humane treatment & well-being of animals at each institution
* have now legal say: can’t prohibit experiments
* activities: advise the staff on animal welfare, the 3R’s , Culture of care, technical and scientific developments, provide policy advises, run campaigns to educate
* members: veterinarians, legal experts, scientists, doctors, animal technicians, facility management, external members, professors
National Committee for Experimental Animals and Alternatives
- advise the competent authorities & animal welfare bodies regarding use of animals in research
Describe who is responsible for compliance in relation how the experiment is performed, and how the animals are housed in the facility. Describe what is expected from the scientist in relation to being aware of local organisation of animal work.
Describe minimum and maximum threshold of pain, suffering, distress or lasting harm, i.e. when a procedure becomes regulated as an animal experiment, and when it cannot be allowed no matter the purpose.
Min:
The injection criterion: a procedure must be licensed if it causes pain, suffering, distress, or lasting harm equivalent to or higher than that caused by the introduction of needle in accordance with good veterinary practice
Max:
Strong pain, other forms of intensive suffering or intensive fear
Never allowed: Procedures causing extreme suffering or pain without potential relief, like extensive
surgery without anesthesia are prohibited, independent from potential benefits
What is meant by destinational breeding in relation animal experimentation legislation, and give examples of some species covered and some species not covered.
Indicate the circumstances in which animals under the scope of the Directive should be humanely killed or removed from the study to receive veterinary treatment, and describe the legislative controls over the killing of animals bred or used for scientific procedures.
If the animal does experience strong pain, intensive suffering or intensive fear, termination is necessary.
Annex four of EU directive:
- table of acceptable and unacceptable methods for euthanasia
- also makes clear that other methods may only be used on unconscious animals not regaining consciousness before death or agricultural research animals if required if required that these are kept under similar conditions to commercial farm animals and in accordance with their EU regulation
- after the killing: death must be ensured by 1) confirmation of permanent cessation of the circulation, 2) destruction of the brain, 3) dislocation of the neck, 4) exsanguination or 5) confirmation of the onset of rigor mortis
Describe how the animal experimentation act is based on an ethical framework which requires 1) weighing the harms and benefits of projects (the harm/benefit assessment) 2) applying the Three Rs to minimise the harm, maximise benefits and 3) promote good animal welfare practices.
Describe the severity classification system, and give examples of each category. Describe cumulative severity and the effect this may have on the severity classification.
Describe the regulations regarding re-use of animals.
Each case of re-use must be approved by the Animal Experiment Inspectorate
* Animals must be in good health & have fully recovered from previous procedures.
* permitted only if the cumulative severity of procedures doesn’t exceed moderate
levels of pain, suffering, or distress.
* There must be a strong scientific justification rather than using a new one
Describe the four functions in relation to educational demands for staff involved in animal experimentation, as well as the role of the manager (EU article 24) and the designated vet (EU article 25).