As the holiday season approaches, please note our adjusted front desk office hours:
This course provides a comprehensive and practical overview of ISO 10006:2017, the international guideline for applying quality management principles within project environments. It is designed for project managers, quality professionals, consultants, and team leaders who aim to improve project predictability, stakeholder satisfaction, and delivery performance by embedding structured quality approaches into all project stages. Participants will learn how ISO 10006 complements ISO 9001, how to apply project-specific quality planning and quality assurance methods, and how to implement systematic controls for scope, resources, communication, risks, and change management. Through real-world examples and templates, this course equips learners to integrate quality thinking into project governance, define project quality objectives, and manage performance indicators aligned with organizational strategy.
By the end of the course, you will be able to:
Understand the scope, structure, and objectives of ISO 10006:2017.
Apply quality management principles to the entire project lifecycle.
Integrate quality planning into project scope, risk, and resource management.
Align project goals with customer needs and organizational strategy.
Establish criteria for quality assurance and quality control in projects.
Define roles, responsibilities, and stakeholder engagement requirements.
Monitor and evaluate project performance using quality indicators.
Document and report on quality outcomes, deviations, and corrective actions.
Integrate ISO 10006 with ISO 9001 or existing project management systems.
Build a roadmap to implement quality-focused project governance.
Project Managers and Program Directors
Quality Assurance and QMS Professionals
PMO and Project Control Specialists
Risk and Compliance Officers
Engineers and Technical Leads managing complex projects
Consultants supporting project-based ISO systems
Basic knowledge of project management methodologies (e.g., PMI, PRINCE2) is helpful
Familiarity with ISO 9001 is beneficial but not required
Ideal for organizations managing capital-intensive or cross-functional projects
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 provides in-depth knowledge of the ISO 13485:2016 standard, designed specifically for organizations involved in the life cycle of medical devices. It guides participants through the structure and requirements of the standard and shows how to implement an effective Quality Management System (QMS) that ensures product safety, regulatory compliance, and customer satisfaction. The training emphasizes risk management, regulatory requirements, process controls, and documentation practices aligned with medical device industry expectations.
By the end of the course, you will be able to:
Explain the purpose, structure, and clause requirements of ISO 13485:2016.
Define the QMS scope and apply a process-based approach for medical device organizations.
Understand risk management principles specific to medical device manufacturing and supply.
Interpret and implement regulatory requirements within the ISO 13485 framework.
Establish documentation, procedures, and controls for design, production, and traceability.
Set up effective monitoring, measurement, and CAPA processes.
Define roles, responsibilities, and training requirements for QMS support.
Integrate supplier control and outsourcing management.
Prepare documentation and records to demonstrate conformity and certification readiness.
Build a roadmap for ISO 13485 implementation across the organization.
Quality Managers and QMS Coordinators in medical device companies
Regulatory Affairs Specialists
Design and Manufacturing Engineers
Internal Auditors and Compliance Officers
Consultants supporting ISO 13485 implementation
Any staff involved in medical device lifecycle management
Understanding of your organization’s medical device processes is helpful
No prior ISO experience is required
Familiarity with regulatory or technical documentation is beneficial