Understand the key upcoming changes in the ISO 9001:2026 version.This course will provide you with an understanding of the current changes and maintain compliance of your current quality management system.

Understand how to conduct Internal Audits against ISO 9001:2026The purpose of this course is to provide learners with the knowledge and skills required to perform an internal audit of part of a Quality Management System (QMS) based on ISO 9001:2026, report on the effective implementation and maintenance of the management system in accordance with ISO 19011:2026 and to contribute to the continual improvement of the QMSTrusted ISO 9001 internal training from a leading course providerOur courses are delivered by tutors who are quality 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 the continuous assessment process.Contact your local SGS office for full details of the courses available in your region.+44 (0) 1276 697704Website: www.sgs.co.uk/trainingscheduleEmail: ukacademy@sgs.comReference MaterialsISO 9001:2026 Quality Management Systems Internal Auditor Training Course Flyer

This course has been developed in alignment with the updated ISO 14001:2026 standard.This course will provide you with an understanding of the current changes and maintain compliance of your current environmental management system.

The objective of this course is to provide learners with the knowledge and skills required to perform an internal audit of part of an Environmental Management System (EMS) based on ISO 14001:2026, report on the effective implementation and maintenance of the management system in accordance with ISO 19011 and to contributeto the continual improvement of the management system.SESSION ONE: Introduction to the ISO 14000 Series of Management System StandardsSESSION TWO: ISO 14001:2026 – Interpretation for AuditSESSION THREE: Audit Definition and PrinciplesSESSION FOUR: Planning and Preparation for the AuditSESSION FIVE: Conducting the AuditSESSION SIX: Audit Reporting and Follow-upSESSION SEVEN: Auditor Competence

This course content is structured in 4 modules and has been developed by SGS to provide Greenhouse Gas and Climate Change practitioners with the necessary skills and knowledge to undertake a verification of a Greenhouse Gas (GHG) inventory developed in accordance with ISO 14064-1:2018 using the verification standard ISO 14064-3:2019Module 1 - Introduction to Climate Change and Greenhouse Gas Accounting and ReportingProviding an introduction to climate change, and to Greenhouse Gas accounting and reporting concepts.Module 2 - Greenhouse Has Protocol Quantification and ReportingIntroduction to ISO 14064-1 and the GHG Protocol. To explore quantification and reporting of Greenhouse Gas emissions. Describing the concepts of GHG inventories, carbon footprints and carbon neutrality.Module 3 - Verification of Greenhouse Gas StatementsIntroduction to ISO 14064-3 and the Verification of Greenhouse Gas Statements by providing a thorough understanding of the Verification Process according to ISO 14064-3 standards. Developing a verification approach which includes a strategic review, risk analysis, verification plan and sampling plans.Module 4 - Validation of Greenhouse Gas StatementsProviding a deeper insight into the validation of Greenhouse Gas Statements in accordance with ISO 14064-3 standards, including verifying removals and net carbon emissions. Exploring the difference between Verification and Validation in the context of ISO 14064-3, ISO 14065 and ISO 14066.Contact Details+44 (0) 1276 697704Website: www.sgs.co.uk/trainingscheduleEmail: ukacademy@sgs.com

The objective of this course is to provide learners with the knowledge and skills required to perform social accountability audits of an organisation’s conformance with social responsibility specifications in accordance with ISO 19011.This course is recognised by APSCA for CPD purposes, aligned with the APSCA Competency Framework.Our courses are delivered by tutors who are Social Accountability 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.

This course is certificated by the Chartered Quality Institute and International Register of Certificated Auditors (CQI/IRCA; Course Certification Number, 2428 - PR 369)This course consists of 10 VILT sessions and the final examination.Course Criteria - ObjectivesUpon completion of this course, learners will be able to:Explain the purpose of a medical device quality management system (MD QMS), interaction with appropriate medical device regulatory authority requirements, quality management systems standard, third-party certification, and the business benefits of the quality management system;Explain the role and responsibilities of an auditor to plan, conduct, report and follow-up a quality management system  in accordance with ISO 19011 (and ISO 17021 where appropriate);Plan, conduct, report and follow-up an audit of a medical device quality management system to establish conformity (or otherwise) with ISO 13485 and applicable medical device regulatory requirement documents in accordance with ISO 19011, ISO/IEC 17021.Learners will need to demonstrate acceptable performance in these areas to complete the course successfully.Prior knowledge Before starting this course, learners are expected to have the following prior knowledge:ISO 13485Knowledge of the requirements of ISO 13485, which may be gained by completing a CQI and IRCA Certified MD QMS ISO 13485:2016 Foundation (FD 132) course or equivalent.Medical Device management System AuditThe Plan, Do, Check, Act (PDCA) cycle.The relationship between ISO 13485 and applicable international regulatory requirements for medical devices.Commonly used quality management terms and definitions within ISO 13485 and ISO 9000.The process approach used in MD QMS.A working knowledge of medical device regulatory process applicable to countries the course is designed to cover, including device regulations, regulatory auditing standards and their relationship with ISO 13485.  This knowledge may be gained by successfully completing a CQI and IRCA course relating to individual regulatory authority standards, which will be available subject to demand (e.g. MD QMS Comprehensive EU Medical Device Regulation 2017/745 (EU MRD) Practitioner - PT 219)A working knowledge of risk management principles related to the design of a medical device, for example ISO 14971

This course is certificated by the Chartered Quality Institute (CQI) and International Register of Certificated Auditors (CQI / IRCA); Course Certification Number, 2142 – PR 366.This course consists of 10 VILT sessions and the final examination.Learners who successfully complete this programme may be eligible to apply for certification by the CQI / IRCA as an auditor, lead auditor or internal auditor within five years of course completion.Other requirements for certification are outlined in this manual and described on the CQI / IRCA website www.quality.org.