In the framework of ensuring a high level of products and in order to increase its competitiveness, the development and implementation of quality management systems at the enterprise can be considered an urgent task. Among the main processes of the QMS, a special place is taken by corrective and preventive actions. Management of this process, in turn, requires regular evaluation of the effectiveness of these activities. The article provides a methodology for evaluating the effectiveness of corrective and preventive actions in the production of solid medicines.

Keywords: corrective actions, preventive actions, unplanned non-conformities, non-conforming products, efficiency analysis