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Simulations of bioequivalence trials using physiological-pharmacokinetic models with saturable and non-saturable hepatic clearance
EUFEPS: WHEN VARIABILITY BECOMES AN ISSUE IN DRUG DEVELOPMENT: HOW TO UNDERSTAND, PREDICT AND MANAGE?
RDF description of Simulations of bioequivalence trials using physiological-pharmacokinetic models with saturable and non-saturable hepatic clearance - http://research.umh.es/vivo/pub/comunicacion/65050