In today’s highly regulated research and production environment, it has become a mainstay to have a thorough and structured investigation process to identify the cause of a quality failure or nonconformity as well as avoid repetition. This is where a Corrective and Preventive Actions (CAPA) manager becomes essential. But what is CAPA management? What are the benefits of the QLIMS CAPA Module? What are the steps of the CAPA process?
What is CAPA?
CAPA (Corrective and Preventive Action) is a module used in quality management to identify and correct problems in a company’s processes, products, or services. The goal of CAPA is to prevent similar issues from occurring in the future. Effective implementation of CAPA helps organizations maintain high standards of quality and customer satisfaction, thus enhancing their reputation and competitiveness in the market.
Many people see CAPAs as a challenging task that must be completed just to stay compliant, but the CAPA manager should be viewed as an end-to-end system that provides the necessary tools to identify, evaluate and investigate incidents. In addition to them, CAPA is essential for implementing and checking the effectiveness of a resolution regarding quality control and regulation.
What is QLIMS CAPA Module and What are The Benefits of It?
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The QLIMS CAPA manager is designed to maintain Corrective and Preventative procedures for general incidents, sample parameters breaching specification and instrument failure incidents, while also integrating with the extensive capabilities of the QLIMS platform.
Here are the benefits of the CAPA Module;
What are the steps of CAPA?
CAPA typically involves a structured and systematic approach to problem-solving, including the investigation of root causes, the development of corrective actions, and the implementation of preventive measures.
Here are the 5 steps of CAPA:
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