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The purpose of this course is to provide participants with an understanding of the management systems approach and the requirements of ISO/IEC 27001. This course may be valuable as preparation if you are planning to complete other ISMS-based training courses, such as the Internal ISMS Auditor Training Course or the ISMS Auditor/Lead Auditor Training Course.Course Content:Introduction to Information Security Management Systems (ISMS) and ISO/IEC 27000 series of standards.ISO/IEC 27001:2022 overview and clauses 4-7.ISO/IEC 27001:2022 clause 8 and risk assessment.ISO/IEC 27001:2022 clauses 9 and 10 and Annex A.Information Security Legislation.Prior Knowledge:​​​​​Before starting the course, you are expected to have the following knowledge:An understanding of the Plan-Do-Check-Act (PDCA) cycle.basic knowledge of the concepts of information security management and an understanding of commonly used information security management terms and definitions, as given in ISO/IEC 27000.

Prerequisites:  Prior knowledge of GMP’s and HACCP, or experience with Food Safety Management Systems, is recommended.FSPCA requires each participant to have your webcam on during the duration of the training.This course developed by the FSPCA is the “standardized curriculum” recognized by FDA; successfully completing this course is one way to meet the requirements for a “preventive controls qualified individual.”The Current Good Manufacturing Practices, Hazard Analysis, and Risk-based Preventive Controls for Human Food regulation (referred to as the Preventive Controls for Human Food regulation) are intended to ensure safe manufacturing, processing, packing, and holding of food products for human consumption in the United States.

ISO/IEC 27001 Lead Implementer training course enables participants to acquire the knowledge necessary to support an organization in effectively planning, implementing, managing, monitoring, and maintaining an information security management system (ISMS).Information security threats and attacks increase and improve constantly. The best form of defense against them is the proper implementation and management of information security controls and best practices. Information security is also a key expectation and requirement of customers, legislators, and other interested parties.This training course is designed to prepare participants in implementing an information security management system (ISMS) based on ISO/IEC 27001. It aims to provide a comprehensive understanding of the best practices of an ISMS and a framework for its continual management and improvement.By enrolling on this course you agree to your personal information being passed to PECB.CertificationAfter successfully passing the exam, you can apply for one of the following credentials with PECB. You will receive the certificate once you comply with all the requirements related to your selected credential.PECB Certified ISO/IEC 27001 Provisional ImplementerPECB Certified ISO/IEC 27001 ImplementerPECB Certified ISO/IEC 27001 Lead ImplementerPECB Certified ISO/IEC 27001 Senior Lead ImplementerGeneral informationParticipants will be provided with the training course material containing over 450 pages of explanatory information, examples, best practices, exercises, and quizzes.Learners may reach out to PECB to request the Attestation of Course Completion as proof of taking the course, this can be requested before taking the exam or after and is worth 31 CPD (Continuing Professional Development) credits.In case candidates fail the exam, they can retake it within 12 months following the initial attempt for free.PrerequisitesThe main requirement for participating in this training course is having a general knowledge of the ISMS concepts and ISO/IEC 27001.The fee for this course covers:Course Materials (for lifetime, please note that updated course materials are not included)First ExamOne resit exam (if required)PECB Certification FeeFirst Year PECB Annual Maintenance Fee (AMF)

This VITAL Training Course provides participants with the skills to perform a VITAL allergen risk assessment and declare cross contact food allergens appropriately. The focus of this course is to showcase how the VITAL Program allows food producers to assess the impact of allergen cross contact and provide appropriate precautionary allergen labelling statements on their products.The VITAL Training Course is designed to complement VITAL Online. This course provides the following:a practical approach to integrating the VITAL Program into an allergen management planan interactive component incorporated throughout the packageopportunity to use VITAL Online, the web-based VITAL Calculatora range of practical examplesopportunities for group discussions.To be successful in understanding the concepts of the VITAL Program, participants need to have a sound grasp of the concepts behind food allergy, allergen labelling, allergen management and allergen analysis.

This course has been developed by SGS for the benefit of learners wishing to understand how to internally audit against FSSC 22000 and its requirements.In May 2026, the scheme was updated from Version 6 to Version 7.This training provides learners with the knowledge and skills required to perform an internal audit of part of a FSMS against FSSC 22000 v7 and ISO 22000:2018, in accordance with ISO 19011:2026, ISO 22002-1:2025, as applicable and contribute to the continual improvement of the management system.Course ContentIntroduction to FSSC 22000 Version 7 (V7)Food Safety Management System (FSMS)Audit Definitions: Principles and TypesRoles and Responsibilities of AuditorsThe Audit ProcessPreparing for the Internal AuditConducting the AuditAudit Review

ISO/IEC 42001 Lead Auditor training course enables you to gain the necessary expertise to audit artificial intelligence management systems (AIMS) by applying widely recognized audit principles, procedures, and techniques.Artificial intelligence (AI) has become integral to the success of many organizations by enhancing efficiency through automation and improving decision-making by utilizing advanced data analytics. However, organizations should ensure the appropriate and ethical use of AI. ISO/IEC 42001 enables organizations to implement appropriate processes and controls to ensure the responsible use and management of AI system.As the number of organizations seeking ISO/IEC 42001 compliance increases, there is a simultaneous surge in demand for skilled auditors possessing the necessary knowledge to assess and verify compliance. Therefore, PECB has developed the ISO/IEC 42001 Lead Auditor training course to empower participants with the knowledge and skills essential for planning and conducting ISO/IEC 42001 audits based on best audit practices.The ISO/IEC 42001 Lead Auditor training course is beneficial for professionals seeking to stay ahead of the competition. This training course equips you with the expertise needed to navigate the intricate realm of AI-influenced organizational frameworks, ensuring you are well-prepared to contribute to the success of organizations in this transformative era.By enrolling on this course you agree to your personal information being passed to PECB.CertificationAfter successfully passing the exam, you can apply for one of the following credentials with PECB. You will receive the certificate once you comply with all the requirements related to your selected credential.PECB Certified ISO/IEC 42001 Provisional AuditorPECB Certified ISO/IEC 42001 AuditorPECB Certified ISO/IEC 42001 Lead AuditorPECB Certified ISO/IEC 42001 Senior Lead AuditorGeneral informationParticipants will be provided with the training course material containing over 450 pages of explanatory information, examples, best practices, exercises, and quizzes.Learners may reach out to PECB to request the Attestation of Course Completion as proof of taking the course, this can be requested before taking the exam or after and is worth 31 CPD (Continuing Professional Development) credits..In case candidates fail the exam, they can retake it within 12 months following the initial attempt for free.PrerequisitesThe main requirement for participating in this training course is having a fundamental understanding of ISO/IEC 42001 and AI principles and concepts.The fee for this course covers:Course Materials (for lifetime, please note that updated course materials are not included)First ExamOne resit exam (if required)PECB Certification FeeFirst Year PECB Annual Maintenance Fee (AMF)

This course is designed to provide manufacturers with an in-depth and practical understanding of Vulnerability Assessment for Food Fraud tools and techniques, and how they can be applied in a practical manner relevant to the participants industry sector.It will enable participants to use techniques to better identify and mitigate risks associated to raw materials in the supply chain. This is particularly useful when implementing product safety management systems and the requirements of the BRCGS Standards onsite.

This course is to provide participants with a thorough understanding of risk assessment and enable them to use different risk assessment models. This is particularly useful when implementing product safety management systems onsite, and when implementing the requirements of the BRCGS Standards.

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 19011:2018 and to contribute to the continual improvement of the management system.The course refers to ISO 14001:2026 as the management system standard that provides the context for an internal audit. However, this course does not address ISO 14001:2026 in detail.Course ContentIntroduction to the ISO 14000 series of management system standardsISO 14001:2026 - interpretation for auditAudit definition and principlesPlanning and preparing for the auditConducting the auditAudit reporting and follow-upAuditor competence

The objective of this course is to provide learners with the knowledge and skills required to perform first-party audits of Occupational Health & Safety Management Systems (OHS) against ISO 45001:2018, in accordance with ISO 19011 and ISO 17021, as applicable.Course ContentIntroduction to occupational health and safety management systemsProcess-based OH&S management systemsAudit evidence and audit trailsAudits: definition, principles and typesThe audit processPreparing for the auditDeveloping a checklistConducting the on-site audit (audit stage 2)Audit reviewRegistration, certification and auditor competence  

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"