Best CAPA Management Software - Qualityze

 


In order to identify the root causes, you can conduct the investigation using more than one investigation tools. Moreover, the risk matrix is been used to assess risk visibility and support the development of action plan. You can select the risk-based, correction, corrective and preventive action plans based on the identified root causes. Qualityze CAPA management software also encourages any organization to verify and validate the quality issues which are identified and tracks the root-cause of the same. This software also documents the problems, potential risks and make relevant solutions.   

  

Qualityze CAPA management software is developed in adherence with industry standards and best practices defined by the regulatory authorities including the Food and Drug Administration (FDA) – 21 CFR Part 820, International Organization for Standardization (ISO) – ISO 9001, ISO 13485 QMS software, Pharmaceuticals and Medical Devices Agency (PMDA), Therapeutic Goods Administration (TGA), China Food and Drug Administration (CFDA), etc.   

  

CAPA management software of Qualityze has an ability to works for all industries that includes Manufacturing, Life Sciences, Pharmaceuticals, Medical Devices, Nutraceuticals, Biologics, Food and Beverages, Automotive, Aerospace, and Defense Logistics, to assess risks and eliminate problems while maintaining compliance with applicable regulatory standards. 

  

 

 

 

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