- CESU
- Initial training, continuing education
- Presential
- 50-60 hours over 2 weeks (February-June each year)
Pharmacometrics is a rapidly evolving and growing field. There is an urgent need of trained experts capable of developing and applying PBPK models with various purposes, such as R&D of new pharmaceuticals, inter-individual variability handling and assessment of toxicological risks. This course will give you the theoretical and technical knowledge to accurately develop, apply and evaluate PBPK models.
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AIMS
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TARGETED STUDENTS
Professionals or PhD students in the fields of pharmacology or toxicology working in the pharmaceutical industry, regulatory agencies, hospitals, research laboratories
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ADMISSION CONDITIONS
Preliminary validation of the CESU "Fundamentals for modelling and simulation in pharmacokinetics/pharmacodynamics" is a prerequisite
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STRUCTURE AND ORGANISATION
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LEARNING SITES
- Faculté de Pharmacie, Marseille timone
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SCHOOL REGISTRATION
Diploma can be access by- Initial Formation (FI)
- Continious formation (FC)
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KNOWLEDGE TO BE ACQUIRED
Concepts include ADME pharmacokinetic parameters, in vitro models, in vitro/in vivo extrapolation, chemical structure-property relationships, model optimization, simulation, parameter sensitivity analysis. Participants will gain technical experience on Matlab Simbiology, Berkeley-Madonna, R, GastroPlus, PKSim and Simcyp in workshops.
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PROFESSIONAL SKILLS TO BE ACQUIRED
After the training, participants should be able to develop, apply and evaluate relevant PKPB models
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PARTNERS
The training will be led by recognized experts in each field, professionals from public teaching and research (France and international: Universities of Aix-Marseille, Athènes (Greece), Liverpool (UK)) and industry (EsqLabs, SimulationsPlus, Phinc, UCBPharma).
