Editable ISO 13485 Audit Checklist Documents

Global Manager Group has offered a ready-to-use ISO 13485:2016 Audit Checklist to comply with Medical Devices manufacturing QMS. A user can use this ready-to-use tool while preparing for ISO 13485 Certification. It has been developed by and is also being used by our ISO 13485 consultants while conducting corporate training sessions and implementing the ISO 13485 system in many pharma and medical device manufacturing companies. The ISO 13485 audit checklist covers more than 900 audit checklist questions based on ISO 13485:2016 clause-wise and department-wise requirements. You can customize this iso 13485 checklist to make your internal audit checklist. The kit is designed to save much of your time in typing and preparing a presentation as well as documentation. To know more, visit here: https://www.globalmanagergroup.com/Products/qms-medical-devices-certification-manual-documents.htm