Service Description

CAPA in pharmaceutical production means "Corrective and Preventive Actions". This is a key element of the quality management system in the pharmaceutical industry. It is designed to identify, correct and prevent the recurrence of problems that may affect the quality and safety of medicines.

CAPA includes the following main aspects:

Problem identification: Identification of deficiencies in processes or products that may lead to deviations from established quality standards.
Investigation of the causes: Analysis of the causes of the problem to determine the root causes. This may include the study of processes, equipment, materials, systems, or the human factor.
Development and implementation of corrective actions: Taking measures to eliminate identified problems and prevent their recurrence in the future. This may include changes in processes, equipment, procedures, or staff training.
Design and implement preventive actions: Identify and implement steps to prevent potential problems from occurring even before they occur.
Monitoring and revision: Continuous monitoring of the effectiveness of measures taken and their revision, if necessary, to ensure continuous quality improvement.