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Global Manager Group provides ISO 13485 Medical Devices QMS Documents in editable format. The ISO 13485 documents contain more than 100 editable MS Word files. These editable documents address all the elements of the medical device quality management system. The entire iso 13485 documents are written in easy-to-understand language. Also, the documentation kit is designed to save much of your time in typing and preparing a presentation as well as documentation. The set of ISO 13485 documents defines the baseline system with an ISO 13485 audit checklist that satisfies standard requirements, which can be customized to suit your requirements. To learn more about the ISO 13485 documents, visit here: https://www.globalmanagergroup.com/Products/qms-medical-devices-certification-manual-documents.htm
ISO 13485, published in 1996, requires a comprehensive quality management system for medical device design and manufacturing. To achieve ISO 13485 cer...
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The ISO 13485 documents provide a ready-to-use solution for quick documentation and easy certification, ensuring a quality system that consistently me...
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