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Business Assurance training courses.

Find a Business Assurance Training Course

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Internal QMS Auditor.

Attending this two day internal auditor course enables you to demonstrate you have the necessary skills to conduct internal audits against ISO 9001:2015 requirements.

Quality
ISO 9001
Auditor

Introduction to ISO 27001:2013 Requirements.

This course explains ISO 27001:2013 and the processes involved in implementing, monitoring, reviewing and improving an information security management system.

ISO 27001
Security

ISO 13485:2016 Auditor/Lead Auditor.

This course details the role & responsibilities of an Auditor/Lead Auditor, including processes & planning, gathering objective evidence and evaluation of findings.

Medical
ISO 13485
Auditor

ISO 27001:2013 Lead Auditor Conversion - CQI & IRCA Certified.

Learn how to audit against ISO 27001 with this three day course, emphasising the importance of information security and how to interpret essential definitions.

ISO 27001
Security
Certified

ISO 45001 Auditor/Lead Auditor - CQI & IRCA Certified.

This five-day course will continue your professional development by enabling you to conduct audits against ISO 45001 requirements.

Health & Safety
ISO 45001
Certified

ISO 45001 Auditor Conversion - CQI & IRCA Certified.

This three day course enables lead auditors to audit occupational health and safety (OH&S) management systems against ISO 45001 requirements.

Health & Safety
ISO 45001
Certified

ISO 45001 Internal Auditor.

Learn how to conduct internal audits, develop checklists and gather objective evidence to evaluate findings and determine conformity and effectiveness against ISO 45001.

Health & Safety
ISO 45001
Auditor
eLearning Available

ISO 45001 Auditor Migration - CQI & IRCA Certified.

This course is for OH&S management systems auditors to improve their external auditing experience or for second and third party auditors wanting ISO 45001 revision.

Health & Safety
ISO 45001
Bestseller
eLearning Available

Implementation of the Medical Device Regulation (MDR).

Learn about the MDR's structure & scope, classification & conformity routes, safety & performance requirements, and developing a post-market surveillance system.

Medical Device Single Audit Program Implementation.

This two day course is for medical device manufacturers who want to be audited once for compliance with the standard and requirements of multiple regulatory authorities.

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