Modeling and simulation in clinical pharmacology and dose finding
- PMID: 23835940
- PMCID: PMC3600758
- DOI: 10.1038/psp.2013.5
Modeling and simulation in clinical pharmacology and dose finding
Abstract
The breakout session 2 of the European Medicines Agency/European Federation of Pharmaceutical Industries and Associations Modeling and Simulation (M&S) workshop focused on two topics: when and how M&S should be used and would be accepted by the authorities for the dose-regimen selection; and when and how M&S can be applied to register a dosing regimen without the need for a specific study. Each topic was introduced by an industry and regulatory perspective, followed by case examples for illustration (Table 1).CPT: Pharmacometrics & Systems Pharmacology (2013) 2, e29; doi:10.1038/psp.2013.5; advance online publication 27 February 2013.
References
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- Jönsson S., Henningsson A., Edholm M., &, Salmonson T. Role of modelling and simulation: a European regulatory perspective. Clin. Pharmacokinet. 2012;51:69–76. - PubMed
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- European Medicines Agency Draft concept paper: Concept paper on extrapolation of efficacy and safety in medicine development . < http://www.ema.europa.eu/docs/en_GB/document_library/ Scientific_guideli... > Accessed 1 October 2012.
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