In vitro models, 13.-22.3.2018
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a dataset collected by the EU Commission in June-September 2018
. Some of these links will therefore die out with time.
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Owner/Developer: University of Tampere (UTA)
| Country: |
Finland |
|---|---|
| Languages: |
English |
| Url: |
https://research.uta.fi/ficam/ |
| Created: |
20 June 2018 |
| Locations: |
Finland |
| City: |
Tampere |
| Description: | 1. Lectures: 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 |
| References: | No publications. Acute toxicity test followed the OECD acute toxicity test and GLP-guidelines |
| Format: |
Hands-on training, Lecture |
| Presence: |
Mandatory, Optional / Voluntary |
| Access: |
Free |
| Content type: |
Theoretical, Practical |
| Duration: |
2 weeks |
| Group size: |
14.0 |
| Frequency: |
Recurrent event |
| Prerequisites: |
For lab work cell culture education and experience. For lectures: no restrictions. Lectures were on advanced level. |
| Target audience: |
Students, Researchers, Regulators and policy-makers, Teachers and educators, Managers, Scientific officers / Project managers, Professionals (e.g. veterinarians) |
| Target sectors: |
Academia, Industry, Governmental bodies, Contract Research Organizations (CROs), Consulting, SMEs |
| Educational level: |
University (Master), University (Doctoral education), Postdoctoral (teaching and research), Continuing Professional Development |
| 3rs relevance: |
Replacement, Reduction |
| Topics covered: |
In vitro methods, Legislative aspects |
| 3rs coverage: |
Full coverage (a dedicated course) |
| Species covered: |
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 |
| Legislative framework: |
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.) |
| Learning outcome: |
Report from group work. GLP-standard report from practical training in the laboratory |
| Qualification received: |
4 ECTS |
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