The objective of this course is to provide learners with an overview of the purpose and requirements of ISO 14001:2026. However, this course does not address ISO 14001:2026 in detail.Course ContentIntroduction to the ISO 14000 series of Management System StandardsISO 14001:2026 Overview and Clause 4ISO 14001:2026 Clauses 5,6 and 7ISO 14001:2026 Clause 8ISO 14001:2026 Clauses 9 and 10

The purpose of this course is to provide learners with knowledge and skill to manage incidents, with specific emphasis on the identification of the root causes and applying the RCAM (root cause analysis method), taking corrective action and implementing control measures to prevent reoccurrences.Course ContentIntroduction to Root Cause Analysis (RCA)Overview of RCAGeneral Principles of RCABenefits of RCAApplying RCAIncident Analysis Tools5 WhysFishbone (Cause and Effect) DiagramFailure Mode and Effects Analysis (FMEA)Incident Cause Analysis Method (ICAM)Bow Tie

This training aims to familiarise learners with auditing management systems guidelines in accordance with ISO 19011:2026.Course ContentSession One: Management Systems AuditingSession Two: Principles of AuditingSession Three: Managing an Audit ProgrammeSession Four: Establishing the Audit ProgrammeSession Five:  Implementing the Audit ProgrammeSession Six: Selecting the Audit TeamSession Seven: Conducting the AuditSESSION EIGHT: Audit ConclusionsPrior KnowledgeNot applicable for this course.Course CertificationOn completion of this course learners will receive a “Certificate of Attendance”.

This single module course has been developed by SGS for the benefit of individuals wishing to understand the changes and amendments transitioning from ISO 19011:2018 to ISO 19011:2026.Course ContentSession 1: ISO 19011:2026 updates and variations to ISO 19011:2018Prior KnowledgeIt will benefit learners if they have knowledge of the ISO 19011:2018 standard.Course CertificationOn completion of this course learners will be issued with a “Certificate of Attendance”.

The purpose of this course is to provide learners with the competency framework to assist in developing, implementing and maintaining a QMS while meeting ISO 9001:2026 requirements.Course ContentIntroduction to Quality Management Systems 9QMS)ISO 9001:2026 StructureInterpretation of Clauses 4 to 10 of ISO 9001:2026Implementation Guidance for ISO 9001:2026

This training aims to familiarise participants with the Technical Documentation requirements of Medical Device Regulation (MDR) (EU) 2017/745, understand what Notified Bodies are looking for and why Technical Documentation needs to be ‘live’ documents which cover the full product life cycle.Course ContentIntroduction to Medical Device Regulation (MDR) and Technical DocumentationLooking at the definition of a medical device, understand what is impacting your Technical Documentation (TD) and why you need to keep your TD up to date, including general requirements associated with TD.Technical Documentation Content (Annex II)Understanding the requirements for Technical Documentation according to Annex II, trying to prepare documents that are new for your company and for a dedicated product, thinking about UDI-DI and basic UDI-DI, classification and associated rationale.Technical Documentation Content (Annex III)Learning to understand the requirements for Technical Documentation in Annex III, including post-market surveillance (PMS), the PMS Plan, PMS Report, and Periodic Safety Update Report (PSUR).Where to StartUnderstanding the importance of performing a gap analysis, conducting a Technical Documentation review, defining the TD structure by identifying areas to focus on and understanding the need for a transition plan.Case StudyTake part in an interactive session to support your understanding and be able to implement the knowledge and skills learnt during the course. This will include tasks on product classification, technical documentation, an MDR gap analysis, team competencies, GSPR matrix and clinical evaluation assessment.How Notified Bodies Assess Technical DocumentationBecome aware of specific areas that Notified Bodies will particularly focus on, understand the TD conformity assessment process described in Annex IX and learn about the assessment criteria that will be applied by Notified Bodies.On completion of this course Learners will be issued with a "Certificate of Attendance"

The aim of this course is to provide learners with the knowledge and skills required to perform first, second and third-party audits of FSMS against FSSC 22000 v7, in accordance with ISO 19011, ISO/TS 22003 and ISO/IEC 17021, as applicable.Learners who complete this CQI and IRCA Certified FSSC 22000 Lead Auditor Training course successfully (within the five years before making an application to become a certificated auditor) will satisfy the training requirements for initial certification as an IRCA FSMS auditor (Part 1) or IRCA FSMS certified auditor (Part 2) of the scheme. For the full requirements, please refer to quality.org/IRCA-grades.Recommended Prior KnowledgeKnowledge of the following food safety management principles and concepts:The Plan, Do, Check, Act (PDCA) cycleThe core elements of a management system and the interrelationship between top management responsibility, policy, objectives, planning, implementation, measurement, review and continual improvement.Food safety management:Knowledge of the principles of food safety management including pre-requisite programmes as specified in ISO 22000:2018 / TS 22002 (all parts) and HACCP;The relationship between food safety management and the provision of food safe products to prevent or minimise adverse effects on human health and the proactive improvement of food safety performance;Awareness of common examples of relevant national and local FSMS legislation and requirements.Knowledge of the requirements of FSSC 22000 v7 or acceptable equivalent, and the commonly used food safety management terms and definitions, as given in ISO 22000:2018, which may be gained by completing a CQI and IRCA certified ISO 22000:2018 (FSMS) training course or equivalent.Enrolment informationBy enrolling on this course you agree to your personal information being passed to CQI and IRCA.DisclaimerFor learners undertaking the CQI and IRCA Online Assessment, all aspects relating to examination, proctoring, disqualification decisions, appeals and the issuance of results to the Approved Training Partner (ATP) are the sole responsibility of CQI and IRCA. SGS does not have oversight of, or involvement in, these processes.Trusted FSSC 22000  training from a leading course providerOur courses are delivered by tutors who are environmental management system experts and experienced trainers. Your knowledge and skills will be developed through an interactive and practical approach to learning. Case study materials and role-play exercises are used to develop and practice skills in all phases of auditing. Participants are continually assessed and required to complete an end-of-course written examination.Contact your local SGS office for full details of the courses available in your region

The purpose of this course is to provide an in-depth knowledge base to support those implementing the AIAG/VDA FMEA Handbook.AIAG and VDA have harmonised their manuals into a single co-copyrighted handbook. The handbook uses the best practices from each manual and a process-oriented approach to meet the requirements of both industry groups, in turn making it easier for automotive manufacturing suppliers to meet the needs of their customers during the failure mode and effects analysis (FMEA) development process.Course ContentPlanning and PreparationStructure and AnalysisFunction AnalysisFailure AnalysisRisk AnalysisOptimisationResults DocumentationConclusion and Knowledge Test

This course has been developed by SGS for the benefit of individuals wishing to understand the changes and amendments transitioning from ISO 19011:2018 to ISO 19011:2026.Course ContentISO 19011:2026 updates and variations to ISO 19011:2018

This training aims to familiarise learners with auditing management systems guidelines in accordance with ISO 19011:2026.Course ContentManagement Systems AuditingPrinciples of AuditingManaging an Audit ProgrammeEstablishing the Audit ProgrammeImplementing the Audit ProgrammeSelecting the Audit TeamConducting the AuditAudit Conclusions

This course is designed to provide participants with the skills and knowledge required to complete non-electrical work safely in the vicinity of a live electrical apparatus. ​ It includes compliance with safe approach distances for the worker, plant, tools and equipment.Course Content:Preparing to work safely in the vicinity of live electrical apparatusIdentify hazardsSafe Approach Distances (SAD)Permit to Work SystemSafety Observers/SpottersPPEElectrical safety regulationsComplete work and documentation​AssessmentThis course includes the following competency-based assessments: A Theory Assessment with multiple choice and short answer questionsPractical Assessment working as a Safety Observer in the vicinity of live electrical apparatus on two occasionsCompleting two JSAs and PermitsDealing with an unplanned event on one occasion