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Advanced Product Quality Planning (APQP) is a framework of linked procedures used for product development in all industries; of particular importance is the automotive industry.This training has been developed by SGS to provide learners with in-depth knowledge about APQP Control Plans compatible with the AIAG APQP Control Plan reference manual (March 2024).

Our Sustainability Reporting Assurance Internal Auditor Course provides with the professional skills required for you to conduct internal audit / review of your organisation’s sustainability reporting. It will also cover the essential skills required for materiality assessment and non-financial reporting. The course helps you appreciate the context of corporate sustainability from the perspective of macrotrends, local guidelines, and the ambition of the integrating sustainability into responsible corporate strategy, policies, and procedures.*There is a requirement of bringing one’s own laptop for physical training. The exercises will be using MS Excel. 

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 in accordance with ISO 19011. This course is recognised by APSCA for CPD purposes, aligned with the APSCA Competency Framework and is worth 40 CPD credits.Recommended Prior KnowledgeBefore starting the course, learners are expected to have knowledge of the following:- SA8000® Standard- Social Accountability International (SAI) Guidance for the SA8000® Standard- Ethical Trading Initiative (ETI) Base Code- The International Labour Organisation (ILO) Standards- UN Human Rights ResolutionsTrusted Social Accountability Lead Auditor 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.Course CertificationOn completion of this course:- Learners who attend the course in full and pass the examination will be issued with a 'Certificate of Achievement' that may satisfy part of the formal training for an individual seeking certification as a Lead Auditor.  Please refer to the relevant auditor certification body for specific requirements.- Learners who attend the full duration of the course will be issued with a 'Certificate of Attendance'.- Learners who fail the examination will be allowed to resit the examination a maximum of two times within 12 months of the end date of the course.

Provide a comprehensive understanding of the GHG Protocol Scope 3 guidance.Equip experienced Scope 1, 2, and 3 practitioners with tangible and practical insights to enhance the assessment and calculation of their company's Scope 3 emissions.Address the key challenges, solutions, and best practices for calculating Scope 3 emissions across the primary categories.Facilitate participant engagement through interactive breakout sessions, hands-on activities, and learning from real-world case studies

The aim of this course is to provide learners with knowledge and understanding of the additional requirements within the Medical Device Regulation (MDR) as well as of the current directives (MDD 93/42/EE) and ISO 13485:2016, including the terminology used and the certification requirements.COURSE CRITERIAUPON COMPLETION OF THIS COURSE, LEARNERS WILL BE ABLE TO:Identify the links between ISO 13485:2016 (QMS) and MDR EU/2017/745;Explain how terminology has changed and where gaps require additional work for Clients to meet the new requirements;Define new requirements for proactive post-market surveillance;Outline the stages of the transition from MDD to MDR so that clients can create individual transition plans;Define the key deliverables for all economic operators.Learners will need to demonstrate acceptable performance in these areas in order to complete the course successfully.PRIOR KNOWLEDGEBefore starting this course, Learners must have a good understanding of the:Current Medical Directives;ISO 13485:2016;Terminology used; andRequirements to achieve certification.

This ISO/IEC 42001 Lead Auditor training course is certificated by PECB and meets the requirements of the PECB Examination and Certification Program (ECP).This course enables learners to gain expertise to audit artificial intelligence management systems (AIMS) by applying widely recognised audit principles, procedures and techniques.

DescriptionThe objective of this course is to provide you with the knowledge and skills required to perform first, second and third-party audits of Information Security Management Systems (ISMS) against ISO/IEC 27001:2022 (with ISO/IEC 27002), in accordance with ISO 19011 and ISO/IEC 17021, as applicable.IRCA AccreditationWe are accredited by the International Register of Certified Auditors (IRCA) globally. This course is accredited by IRCA, reference number 2549 - PR 373.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.

The objective of this course is to provide learners with the knowledge and skills required to perform internal audits of management systems based on the requirements of ISO 9001:2015, ISO 14001:2026 and ISO 45001:2018 (or equivalent), and report on the effective implementation and maintenance of the management system in accordance with ISO 19011.Course detailsDuration: 3 daysAccreditation: SGS certificate of attendance upon completionPrior KnowledgeBefore starting this course, learners are expected to have the following prior knowledge:▪ Management Systems:▪ Quality, environmental and OH&S management:▪ ISO 9001:2015, ISO 14001:2026 and ISO 45001:2018:Course ContentProcess-based QMSAuditing for Continual ImprovementIntroduction to EMS AuditingISO 14001:2026 Interpretation for AuditIntroduction to OH&S MSRisk Assessment: Tools, Techniques and ControlsAudits: Definitions and PrinciplesPlanning and Preparing for the AuditConducting the AuditAudit Reporting and Follow-upAuditor Competence

ISO 59020 provides organisations a framework to measure and assess their circularity performance at the organisational and product levels. This 1-day online and offline (VILT) training program is designed to help participants understand the growing business case for circular and sustainable solutions and learn how to incorporate circular economy principles into business strategies.*There is a requirement of bringing one’s own laptop for physical training. The exercises will be using MS Excel.

Through a series of discussion-based sessions and interactive workshops, learn how to help your organisation demonstrate Good Manufacturing Practice (GMP) compliance using ISO 22716.  Build a strong foundation of knowledge and skills. Course Topics:Overview of GMP and the StandardClause 3: Personnel RequirementsClause 4 and 5: Premises and Equipment RequirementsClause 6 and 12: Raw and Packaging Materials including subcontracting RequirementsClause 7 and 8: Production and Finished products requirementsClause 9: Quality Control Laboratory requirementsClause 10, 11 and 13: Treatment of product that is out of specification including Deviations and Waste management requirementsClause 14: Complaints and recalls requirementsClause 15 and 17: Change Control and Documentation requirementsClause 16: Internal audit requirementsLearning Review and Summary

Through interactive workshops and audit role play, learn to audit your Cosmetic GMP's, according to ISO 22716:2007 and ISO 19011:2018 guidance.Course Topics:Clause 3: Personnel RequirementsClause 4 and 5: Premises and Equipment RequirementsClause 6 and 12: Raw and Packaging Materials including subcontracting RequirementsClause 7 and 8: Production and Finished products requirementsClause 9: Quality Control Laboratory requirementsClause 10, 11 and 13: Treatment of product that is out of specification including Deviations and Waste management requirementsClause 14: Complaints and recalls requirementsClause 15 and 17: Change Control and Documentation requirementsClause 16: Internal audit requirementsHow to Audit According to ISO 19011Learning Review and Summary