Advanced course:
Toxicology as the Scientific Basis for Management
of Chemical Risk
Toxicology as the Scientific Basis for Management
of Chemical Risk
I. Interpretation and integration of repeated dose toxicity data
Leuven, 8 October, 2010
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8.30-9.00
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Reception and coffee
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9.00-9.15
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Introduction to the seminar
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Mark Martens/Peter Hoet
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9.15-10.00
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Part 1: Toxicity testing: what are the studies and how is a testing program set up
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Marie-Louise Meisters
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10.00-12.30
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Part 2: Selected components of a toxicology study
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| 10.00-10.30 | * Toxicokinetics | Peter Hoet |
| 10.30-11.00 |
Coffee break |
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11.00-11.30 |
* Clinical and other observations | Koen van Deun |
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11.30-12.15 |
* Haematology and clinical chemistry | Mark Martens |
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12.15-13.00 |
* Necropsy and histopathology | Sandra De Jonghe |
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13.00-13.45
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Lunch break
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13.45-14.30
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Part 3: How to conclude on the relevance of observed effects. Integration of human data
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Dominique Lison
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14.30-16.00
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Part 4: Case studies – participants to split up into 8 groups and work through various data sets. Objective conclude on the effects observed
(coffee available throughout part 4) |
Jacques de Gerlache
Each working group will have a coach |
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16.00-17.00
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Report from the various groups
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Selected group speaker
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17.00-17.30 |
Feedback on the reports and general discussion | Teaching Team |
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17.30
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End of the day
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