In vitro models, 13.-22.3.2018 (In vitro models, 13.-22.3.2018)
Owner/Developer: University of Tampere (UTA)
20 June 2018
Lecture 1: General information about the course and principles of in vitro models (2h)
Lecture 2: How to ensure relevance and quality of in vitro models (1,5 h)
Lecture 3: Assessing safety and efficacy with in vitro models (2h)
Lecture 4: Body/tissue-on-chip models (1h)
Lecture 5: In vitro cancer models (1h)
Lecture 6: In vitro bone and bone metastasis model (1h)
Lecture 7: In vitro models in ophthalmological applications (2h)
Lecture 8: In vitro neuronal models (2h)
Lecture 9: In vitro models in cardiac applications (1h)
Lecture 10: Group work presentations (4h, length depends on the number of groups presenting)
Lecture 11: The theory of acute toxicity test, standard operation procedures and study plans (2h, )
2. Group work and presentation of chosen in vitro model
3. Acute toxicity test, written study plan, laboratory diary according to GLP and study report
No publications. Acute toxicity test followed the OECD acute toxicity test and GLP-guidelines
Hands-on training, Lecture
Mandatory, Optional / Voluntary
For lab work cell culture education and experience. For lectures: no restrictions. Lectures were on advanced level.
Students, Researchers, Regulators and policy-makers, Teachers and educators, Managers, Scientific officers / Project managers, Professionals (e.g. veterinarians)
Academia, Industry, Governmental bodies, Contract Research Organizations (CROs), Consulting, SMEs
University (Master), University (Doctoral education), Postdoctoral (teaching and research), Continuing Professional Development
In vitro methods, Legislative aspects
Full coverage (a dedicated course)
No species is addressed specifically
|Details on the topic or technology covered:||
Cellular, organ and tissue models, organ-on-a-chip technolgy, toxicity and disese models
Directive 2010/63/EU or equivalent, CLP Regulation (EC) No 1272/2008, REACH Regulation (EC) No 1907/2006 or equivalent, Cosmetics Regulation (EC) No 1223/2009 or equivalent, Plant Protection Products Regulation (EC) No 1107/2009, 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), Food Safety (EC) No 178/2002 or equivalent, Test guidelines (OECD, ISO, etc.)
Report from group work. GLP-standard report from practical training in the laboratory
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