ISO 13485 2016 documents contain more than 100 editable MS Word files. These editable documents address all the elements of the medical device quality management system. Global Manager Group has designed a ready-to-use ISO 13485 2016 documents kit to comply with Medical Devices manufacturing QMS. Our ISO 13485 documents include the ISO 13485 Quality Manual, ISO 13485 procedures, SOPs, formats, and ISO 13485 audit checklist.
To know more, visit here: https://www.globalmanagergroup.com/Products/qms-medical-devices-certification-manual-documents.htm
