Fully Customizable CAPA Form

1. Fully Customizable CAPA Form When it comes to a business or organization, productivity is everything. The more productive you're in all areas of your company the more successful you will be in the future. Fortunately, CAPA - Corrective and Preventative Action - can help! What is the definition of CAPA Software? It is an abbreviation of corrective action and preventative action software which can be considered a vital tool designed for any business quality management system. In simple words, this is a kind of software that allows personnel to record and keep track of corrective action requirements in whatever form they take. Such software can be used to track customer service complaints, employee complaints, supplier non-conformance, or virtually anything else which needs deliberate action.

2. It keeps the issues extremely visible in order to force the user to solve them. It also allows the user to connect relevant images or other information in order to better organize the corrective action requirements. By allowing the linking of information, contacts, and cross-references, the software helps the user determine the right course of action and therefore the proper personnel to notify. Below are the defining steps of the CAPA system include – (i) Root Cause Analysis: This is the primary step to the application of the CAPA process, and it's to do with laboratory analysis or a close audit of documents that relate to the problem or complaint. This identifies the particular problem for the later stages of the process. (ii) Identification and Adaptation of Corrective Action: These are the immediate steps to address a present complaint; which may have to do with product replacement, and various steps to provide relief to any persons directly affected by a faulty product. (iii) Development and Adaptation of Preventive Action: In CAPA for Pharma, developing a preventive action indicates the various steps for addressing a complaint or discrepancy on a long term basis. This may include decisions like a product recall, or rectification of a regular system. (iv) Implementation of Preventive Action: The final stages to the CAPA Medical Device, implementing a preventive action ensures that future incidents relating to a complaint or discrepancy are prevented. In the year 2005, the company named Orcanos comes into existence by Zohar Peretz and Rami Azulay. The one and the only company that provides integrated software for quality management (QMS) and ALM (Design Control) combined with regulations compliance. ORCANOS CAPA (Corrective Action and Preventive Action), as a part of Orcanos QMS, ensure regulations compliance, while automating the CAPA process completely, from initiation to investigation and closure. With years of proven experience in a regulated hi-tech industry, operating with medical device manufacturers makes Orcanos unique from others. For more details and to know about Orcanos or more please, call us at +972- 3-5372561 or visit our website HERE; https://www.orcanos.com/compliance/