What’s the Purpose of Maintaining Nonconformance Records?

During the process of nonconformance management process, the organization identifies nonconformance, records relevant data and then creates an action plan for either getting the nonconformances up to the standards or disposing of nonconforming materials. Nonconformance management software of Qualityze comes with alerts and notifications capability which automatically notifies the quality teams whenever the quantity of raw materials reaches below threshold quantity. Read more - https://www.qualityze.com/nonconformance-management/ Nonconformance Management software of Qualityze works for every industry, including – Manufacturing, Life Sciences, Pharmaceuticals, Medical Devices, Cannabis/Hemp/CBD, Nutraceuticals, Biologics/Biotech, Food and Beverages, Automotive, Aerospace, Defense and Logistics, to identify, document, and resolve quality problems while maintaining compliance with applicable federal and state regulatory standards. Qualityze Nonconformance management software solution complies to the industry-specific standards including ISO 9001, ISO 13485, 21 CFR Part 11, 21 CFR Part 820, AS9100, and IATF 16949 to ensure that only best practices are followed. This software has the automated email approval, alerts and notifications, reports and dashboards and other built-in capabilities which makes the nonconformance process faster and smarter.


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