Education for persons planning and performing experiments and killing experimental animals
This record is part of
a dataset collected by the EU Commission in June-September 2018
. Some of these links will therefore die out with time.
Please see the
overview of courses maintained by ETPLAS
or contact Norecopa for more information.
Owner/Developer: Polish Laboratory Animal Science Association (PolLASA)
Country: |
Poland |
---|---|
Languages: |
Polish |
Url: |
http://pollasa.pl |
Created: |
05 October 2015 |
City: |
Puławy |
Format: |
Lecture, Workshops |
Presence: |
Mandatory |
Access: |
Free |
Content type: |
Theoretical |
Duration: |
14h to 25h |
Frequency: |
Recurrent event |
Prerequisites: |
FOR THOSE PARTICIPATING IN THE EXECUTION OF THE PROCEDURE - 14 h, FOR PEOPLE PERFORMING PROCEDURES - 21 h, FOR PETS KILLERS ANIMALS USED IN THE PROCEDURE - 10 h FOR THOSE CARING FOR ANIMALS RETAINED IN THE CENTER - 15 h, FOR PERSONS RESPONSIBLE FOR SUPERVISION OF PERSONS THAT MAKE CARE OF ANIMALS RETAINED IN THE CENTER AND THE WELFARE OF THOSE ANIMALS - 25 h. |
Target audience: |
Researchers, Technicians, Scientific officers / Project managers, Professionals (e.g. veterinarians) |
Target sectors: |
Industry, Governmental bodies |
Educational level: |
Technical College, University (Bachelor), University (Master), University (Doctoral education), Postdoctoral (teaching and research) |
3rs relevance: |
Refinement, Reduction, Replacement |
Topics covered: |
Models of animals (e.g. mannequins, simulators, cadavers), Carrying out procedures on animals, Designing procedures and projects, Taking care of animals, Killing animals, Computational methods, In vitro methods, Ethics, Legislative aspects |
3rs coverage: |
Substantial coverage (e.g. multiple modules) |
Species covered: |
No species is addressed specifically |
Course level on animal species: |
Introductory course, Basic course, Advanced course |
Legislative framework: |
Directive 2010/63/EU or equivalent, Biocidal Products Regulation (EC) No 528/2012, Medical Devices Regulation (EU) 2017/745, In Vitro Diagnostic Medical Devices Regulation (EU) 2017/746, International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use (ICH), EU & US Pharmacopoeia, Test guidelines (OECD, ISO, etc.) |
Accreditation body and/or authority that approved the education or training: |
PolLASA |
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