This Video Explain the requirement of Clause 8 of ISO 13485:2016 which covers the requirement ISO 13485 for Medical devices — Quality management systems Auditor. This content is useful for MD-QMS (13485:2016) Internal Auditor, Auditor, Lead Auditor, Implementer, Lead Implementer. This video includes an explanation of the requirement of Clause 8 of 13485:2016. The further explanation has been made in consideration with the requirement of ISO 19011-2018 and ISO 17021-1-2015 to enable the audience to provide the knowledge of management system standards to become an efficient auditor. In this video/session, we discussed Clause 8 of 13485:2016 that states the process of communicating vital information related to the Medical devices — Quality management systems of the organization internally and externally. This video is useful to understand Clause 8 of ISO 13485, ISO 13485:2016, ISO 13485 clause wise explanation. 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