Training Course

Automotive Quality

IATF 16949 Requirements Training Course

Information Security

Internal Auditor ISO/IEC 27001:2013 training course

Aerospace and Aviation

AS/EN/JISQ 9100:2016 Aerospace Lead Auditor Training Course

Aerospace and Aviation

AS/EN/JISQ 9100:2016 Implementing Training Course

Aerospace and Aviation

AS/EN/JISQ 9100:2016 Internal Auditor Training Course

Aerospace and Aviation

AS/EN/JISQ 9100:2016 Requirements training course

Building information modelling - ISO 19650, PAS 1192

BIM BS 1192 Part 4: Handover Information Exchange training course

BIM - Building Information Modelling

BIM PAS 1192 Part 3: Asset Management training course

Building information modelling - ISO 19650, PAS 1192

BIM PAS 1192 Part 5: Security and BIM training course

Building information modelling - ISO 19650, PAS 1192

BIM PAS 1192 Part 6: Health and Safety Training Course

BIM - Building Information Modelling

Building Information Modelling (BIM) Fundamentals Training Course

BIM - Building Information Modelling

Building Information Modelling (BIM) ISO 19650 Part 2: Project Delivery Training Course

Medical Devices

Clinical Evaluation for Medical Devices Training Course

Environmental Management

CQI and IRCA Certified ISO 14001:2015 Lead Auditor Training course (17903)

Quality Management

CQI/IRCA Certified ISO 9001:2015 Lead Auditor Training Course (17955)

Automotive Quality

IATF 16949 Quality Management Systems Internal Auditor Course

Automotive Quality

IATF 16949:2016 Implementation Training Course

Medical Devices

Implementation of MDR for CE marking

Medical Devices

Implementation of Medical Device Regulation for CE Marking Training Course

Medical Devices

Implementation of the In Vitro Diagnostic Device Regulation for CE Marking Training Course

Business Continuity Management

Implementing an ISO 22301 Business Continuity Management System

Medical Devices

Implementing ISO 13485:2016 Training Course

Information Security

Implementing ISO/IEC 27001:2013 training course

Information Security

Information Security Management Systems Auditor/Lead Auditor CQI/IRCA Certified Course (17287)

Medical Devices

Internal Auditor ISO 13485:2016 Training Course

Medical Devices

Introduction ISO 13485:2016 Training Course

Business Continuity Management

Introduction to ISO 22301 Business Continuity Management

Medical Devices

Introduction to Medical Device Software Training

Performance Improvement

Introduction to the UN Sustainability Development Goals

Medical Devices

ISO 13485:2016 Requirements On-demand eLearning

Environmental Management

ISO 14001 Requirements Training Course

Environmental Management

ISO 14001:2015 Implementation course

Environmental Management

ISO 14001:2015 Internal Auditor Course

Environmental Management

ISO 14001:2015 Requirements On-demand eLearning Training Course

Medical Devices

ISO 14971 Requirements training course

Medical Devices

ISO 14971:2019 Risk Management for Medical Devices: Requirements Training Course

Business Continuity Management

ISO 22301 Business Continuity Management Internal Auditor

Business Continuity Management

ISO 22301 Business Continuity Management Lead Auditor

Business Continuity Management

ISO 22301:2019 Requirements On-demand eLearning

Health and Safety

ISO 45001 Implementation Training Course

Health and Safety

ISO 45001 Internal Auditor Training Course

Health and Safety

ISO 45001 Requirements on-demand eLearning Training Course

Health and Safety

ISO 45001 Requirements Training Course

Energy Management

ISO 50001:2018 Requirements On-demand eLearning

Quality Management

ISO 9001:2015 Implementation

Quality Management

ISO 9001:2015 Internal Auditor Training Course

Quality Management

ISO 9001:2015 Requirements On-demand eLearning

Quality Management

ISO 9001:2015 Requirements Training Course

Privacy management

ISO/IEC 27701 Implementation training course

Privacy management

ISO/IEC 27701 Internal Auditor training course

Privacy management

ISO/IEC 27701 Requirements training course

Medical Devices

IVD Directive to IVD Regulation (IVDR) Transition training course

Medical Devices

Manufacturing Process Validation for Medical Devices: Introduction to Concepts and Methods

Medical Devices

Medical Device Single Audit Program (MDSAP):Fundamentals and Readiness

Medical Devices

Medical Devices – Quality Management Systems Auditor/Lead Auditor Training Course ISO 13485:2016

Medical Devices

Medical Devices Directive (MDD) to Medical Devices Regulation (MDR) Transition training course

Health and Safety

OH&S Management Systems Auditor/Lead Auditor - CQI/IRCA Certified Course (17036)

Medical Devices

Post Market Surveillance and Vigilance under MDR and IVDR

Process Improvement

Process Improvement: Auditor Training Course

Process Improvement

Process Improvement: Introduction Training Course

Auditing

Remote Auditing Training Course

Information Security

Requirements of ISO/IEC 27001:2013

Information Security

Requirements of ISO/IEC 27001:2013 On-demand eLearning

Medical Devices

Requirements of the In Vitro Diagnostic Regulation Training Course

Medical Devices

Requirements of the MDR for CE Marking Training Course

Medical Devices

Requirements of the Medical Device Regulation for CE Marking Training Course

Medical Devices

Technical Documentation for In Vitro Diagnostic Devices (IVDs)

Medical Devices

Technical Documentation for the MDR Training Course

Health and safety management - ISO 45001, ISO 45003, ISO/PAS 45005

Understanding ISO/PAS 45005