Introduction: Cystic Fibrosis (CF) is a heritable chronic condition. Due to the genetic and progressive nature of CF, a number of interventions are available for the condition. In the United Kingdom (U.K.) average cost of CF treatment is between €49,000 to €76,000 1 per patient (1). A review of health economic modelling studies is warranted to provide decision makers and researchers with an in depth understanding of modelling practices in CF and guidance for future research.Methods: Online searches were performed in the 5 databases, studies were included if they were: 1) Model based economic evaluation for management of Cystic Fibrosis.Articles were restricted to English language only, but no restriction was applied on publication year.Results: Nine studies were reviewed, most were Markov cohort models. Models evaluated pharmaceutical interventions and drug adherence. Modelling structure was consistent across most articles and a range of sources were used to populate the models. Cost and utility data were based on different sources and elicitation methods respectively. The majority of models failed to incorporate significant health events which impact both cost and disease progression. 1 2012