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This course provides a practical understanding of ISO 29001:2020, the sector-specific Quality Management System standard for organizations in petroleum, petrochemical, and natural gas supply chains. Participants learn how to establish and maintain processes that reduce operational risks, strengthen supply-chain performance, and ensure product and service conformity in high-risk environments. The course addresses process-based thinking, defect prevention, variability reduction, and critical quality controls required for equipment, materials, and services used in oil and gas operations. Trainees will gain the ability to align ISO 29001 requirements with ISO 9001 principles to enhance regulatory compliance, reliability, safety, and long-term operational excellence.
By the end of the course, you will be able to:
Understand the structure and intent of ISO 29001 and its relationship to ISO 9001.
Define the scope of the QMS based on sector-specific risks and compliance needs.
Interpret and apply requirements from clauses 4 to 10 of ISO 29001.
Implement controls for defect prevention, nonconformity management, and risk mitigation.
Develop quality objectives, KPIs, and performance tracking tools relevant to oil & gas.
Integrate design, development, production, and service controls.
Manage documented information, supplier evaluation, and customer satisfaction.
Establish internal audit, management review, and corrective action processes.
Prepare a phased implementation plan leading to ISO 29001 certification.
Align your QMS with industry-specific regulatory and customer requirements.
QHSE Managers and Quality Professionals in oil & gas
Project Managers and Process Owners
Engineers and Technical Supervisors
Procurement and Supplier Quality Leads
Internal Auditors and Compliance Officers
Consultants supporting ISO 29001 implementation
Familiarity with ISO 9001 or quality system principles is helpful
No prior ISO 29001 experience required
Industry experience in petroleum, gas, or petrochemicals is beneficial
This course equips participants with the knowledge and skills to perform effective internal audits of a Quality Management System (QMS) in accordance with ISO 13485:2016. Designed for organizations involved in the medical device lifecycle, the training focuses on assessing conformity with the standard’s requirements, regulatory expectations, and risk-based controls. It also integrates ISO 19011 audit principles and provides practical techniques for planning, executing, and reporting internal audits that support certification and continual improvement.
By the end of the course, you will be able to:
Understand the structure and key requirements of ISO 13485:2016.
Explain the internal audit process based on ISO 19011:2018.
Plan internal audits based on process, risk, and regulatory focus areas.
Develop audit checklists and gather objective evidence through records and interviews.
Assess implementation of procedures, documentation, traceability, and control of outsourced processes.
Identify nonconformities and generate clear, actionable audit findings.
Write professional audit reports and communicate results to stakeholders.
Follow up on corrective actions and verify effectiveness.
Contribute to continual improvement and readiness for regulatory inspections or certification audits.
Evaluate supplier audits and integration into the internal audit program.
Internal Auditors in medical device organizations
QMS Coordinators and Quality Assurance Staff
Regulatory Compliance Officers
Manufacturing and Operations Managers
Design and Development Engineers
Consultants supporting ISO 13485 compliance
Familiarity with ISO 13485:2016 or your organization’s medical device QMS is helpful
No prior internal audit experience is required
Basic understanding of medical device regulatory context is beneficial
A practical, scenario-based course that builds the competence to plan, conduct, report, and follow up internal audits of an Occupational Health & Safety Management System (OHSMS) aligned to ISO 45001:2018, using the ISO 19011 auditing guideline as your roadmap. You’ll practice process- and risk-based auditing, worker participation touchpoints, evidence gathering, and clear reporting that drives corrective action and prevention. (ISO 45001 replaces OHSAS 18001 and places a stronger emphasis on worker participation). You’ll also learn how to structure an audit program and assign competent, independent auditors in accordance with ISO 19011.
This course is designed to equip participants with the skills and knowledge needed to conduct effective internal audits of an Information Security Management System (ISMS) based on ISO/IEC 27001:2022. It integrates the auditing principles of ISO 19011 with the specific requirements of ISO 27001, enabling participants to assess conformity, effectiveness, and continual improvement of information security controls. Real-world audit exercises and reporting templates help bridge the gap between theory and practice.
By the end of the course, you will be able to:
Understand ISO/IEC 27001:2022 clause structure and the purpose of an ISMS.
Explain the internal audit process in accordance with ISO 19011.
Plan internal audits based on risk, scope, and objectives.
Develop audit checklists and gather evidence through interviews, records, and observation.
Evaluate implementation of information security controls (Annex A).
Identify nonconformities, opportunities for improvement, and best practices.
Write clear, objective audit reports aligned with organizational requirements.
Support management review, corrective action, and continual improvement.
Assess audit effectiveness and follow up on previous audit results.
Prepare for certification and surveillance audits through internal audit readiness.
ISMS Coordinators and IT Managers
Internal Auditors and Risk Officers
Compliance Managers and Data Protection Officers
Cybersecurity and Governance Professionals
Consultants supporting ISO 27001 implementation or audits
Anyone involved in internal audit or information security roles
Familiarity with ISO/IEC 27001:2022 or general information security principles is helpful
No prior auditing experience is required
Some technical understanding of IT and data management is beneficial
A practical, workshop-style course that equips you to plan, conduct, report, and follow up internal audits of an ISO 50001 EnMS. You’ll apply process- and risk-based auditing to the full energy cycle—energy review, significant energy uses (SEUs), operational controls, design/procurement, and performance monitoring. Learn to evaluate EnPIs/EnBs and normalization logic, test M&V approaches, write clear nonconformity statements with strong evidence, verify corrective actions, and manage opening/closing meetings and concise audit reports. Includes tips for remote/hybrid audits and Canadian/BC context for utilities and regulatory considerations [Verify].
A practical, workshop-style course that equips you to plan, conduct, report, and follow up internal audits of an ISO 14001 EMS. You’ll apply process- and risk-based auditing, use effective sampling and interviewing techniques, write clear nonconformity statements with supporting evidence, evaluate root causes and corrective actions, and manage opening and closing meetings and audit reports. We also cover auditing environmental aspects/impacts, compliance obligations, emergency preparedness, contractors/outsourced processes, life-cycle thinking, and remote/hybrid auditing.
This course provides a structured approach to understanding and applying the requirements of ISO 22000:2018 for developing a robust Food Safety Management System (FSMS). It combines theoretical principles with practical tools to help you design, document, and implement an FSMS that ensures safe food practices, manages risks, and meets customer and regulatory expectations. All activities are mapped to clauses 4–10 of the standard, enabling participants to build systems that support hazard control, compliance, and continual improvement.
By the end of the course, you will be able to: