AbstractThe validity of any model depends on its ability to imagine the situation or problem to which it is applied. Further, the assumptions made in relation to the model are determining for the actual outcome. Within the field of clinical biochemistry a lot of models for analytical quality specifications, based on a variety of concepts and clinical settings, have been proposed. A hierarchical structure for application of these approaches and models has been agreed on at several occasions in 1999. In this hierarchy, the highest rank is given to evaluation of analytical quality specifications based on clinical settings/clinical outcome models, followed by specifications based on biological variation and on clinicians opinions. This contribution, deals with the problems of combining random and systematic errors and the implications of application of different models to a variety of clinical settings.