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2. ISO/IEC 27001 Lead Auditor - Wikipedia

   en.wikipedia.org/wiki/ISO/IEC_27001_Lead_Auditor

   The ISO/IEC 27001 Lead Auditor certification consists of a professional certification for auditors specializing in information security management systems (ISMS) based on the ISO/IEC 27001 standard and ISO 19011. The training of lead auditors normally includes a classroom/online training and exam portion and a requirement to have performed a ...

3. Lead auditor - Wikipedia

   en.wikipedia.org/wiki/Lead_Auditor

   Most publicly traded corporations typically have an internal auditing department, led by a chief audit executive ("CAE"), with lead internal auditors managing small teams of internal auditors for one audit engagement. [1] Lead auditor is a position between senior auditor and head of division. In public accounting firms, a lead auditor for an ...

4. ISO/IEC 27001 - Wikipedia

   en.wikipedia.org/wiki/ISO/IEC_27001

   The ISO/IEC 27001 certification, like other ISO management system certifications, usually involves a three-stage external audit process defined by ISO/IEC 17021 [7] and ISO/IEC 27006 [8] standards: Stage 1 is a preliminary review of the ISMS. It includes checks for the existence and completeness of key documentation, such as the organization's ...

5. ISO/IEC 27000 family - Wikipedia

   en.wikipedia.org/wiki/ISO/IEC_27000_family

   ISO/IEC 27013 — Guidance on the integrated implementation of ISO/IEC 27001 and ISO/IEC 20000-1: brings together the management systems for information security and IT services. ISO/IEC 27014 — Governance of information security [ 11 ] : Mahncke assessed this standard in the context of Australian e-health.) [ 12 ]

6. Category:ISO/IEC 27001 - Wikipedia

   en.wikipedia.org/wiki/Category:ISO/IEC_27001

   Download as PDF; Printable version; In other projects Wikidata item; Appearance. ... ISO/IEC 27001 Lead Auditor; ISO/IEC 27001 Lead Implementer This page was ...

7. ISO 13485 - Wikipedia

   en.wikipedia.org/wiki/ISO_13485

   ISO 13485 Medical devices -- Quality management systems -- Requirements for regulatory purposes is a voluntary standard, [1] published by International Organization for Standardization (ISO) for the first time in 1996, and contains a comprehensive quality management system for the design and manufacture of medical devices.