Webinar: Corrective and Preventive Actions – October 20, 2022 at 14:00 CET (75 min)
In this webinar, we will show you how our software facilitates effective CAPAs by turning dead-end data into live information. Learn how it helps you to identify, investigate, record, and analyze the root causes of a non-conformance and put in place a bulletproof CAPA system in your company. This webinar will be held in English.
Does the acronym CAPA sound familiar to you? Does it cause you headaches? Then you’re probably not alone. Search the FDA’s notorious database of Warning Letters and you’ll be overwhelmed by the results that deal with Corrective and Preventive Actions – they are quite frankly a perpetual cause of anxiety for many quality management professionals all around the globe.
Software for Corrective and Preventive Actions
Let us introduce you to our CAQ.Net® software solutions in our webinar on October 20, 2022 at 14:00 CET. Learn how we can help you put in place a dedicated CAPA system that also aims to prevent non-conformities from occurring in the first place. See how our software provides you with a platform from where you are able to view the entire production process, from supplier selection and incoming goods inspection to quality inspection and complaints processing and have all necessary data available at all times.
What is CAPA?
Initially featured in the FDA’s Quality System Guidance in 2006 and now a prerequisite of the FDA’s 21 CFR 820 as well as ISO 13485, GMP, and ICH guidelines, the Corrective And Preventive Actions concept today is an integral aspect of contemporary medical device and pharmaceuticals industries. Its aim is to identify the possible causes of quality defects that have occurred, to solve them, and to adapt workflows, products, or manufacturing processes to prevent the defect from recurring.