- ACS Academy
- Flexible Learning, Lasting Success
-
- info@acs-academy.ca
- (604) 924-5506 ext.377
- 318-901 Third Street West, North Vancouver, BC, V7P 3P9
As the holiday season approaches, please note our adjusted front desk office hours:
This comprehensive course provides the knowledge, practical tools, and implementation strategies required to establish, implement, maintain, and continually improve an Asset Management System (AMS) in accordance with ISO 55001:2024.
Participants will gain a thorough understanding of asset management principles, the requirements of ISO 55001, and internationally recognized best practices for managing physical assets throughout their lifecycle. The course combines theory with practical implementation techniques, enabling organizations to improve asset performance, reduce lifecycle costs, manage risks, and support long-term organizational objectives.
The course covers the complete implementation process from organizational context through leadership, planning, support, operation, performance evaluation, and continual improvement, while preparing participants for successful certification.
By the end of this course, you will be able to:
A practitioner-focused course that shows participants how to understand, design, implement, and maintain an Environmental Management System aligned with ISO 14001:2026. The course follows the PDCA model and translates the requirements of ISO 14001 into practical actions that organizations can apply to improve environmental performance, meet compliance obligations, reduce environmental risks, and support sustainability goals.
Participants will learn how to determine organizational context, identify relevant interested parties, define the EMS scope, establish environmental policy and objectives, evaluate environmental aspects and impacts, address risks and opportunities, and develop practical operational controls. The course also explains how to manage documented information, competence, awareness, internal and external communication, emergency preparedness, monitoring and measurement, evaluation of compliance, internal audits, management review, nonconformity, corrective action, and continual improvement.
Special attention is given to the 2026 revision, including stronger alignment with the latest ISO management system structure, clearer expectations around environmental conditions, climate change, biodiversity, ecosystem health, compliance obligations, life cycle perspective, risk-based planning, and integration with other systems such as ISO 9001, ISO 45001, and ISO 50001.
By the end of this course, participants will be able to:
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
A practitioner-focused, hands-on course that demystifies ISO 50001 and shows you how to design, implement, and sustain an Energy Management System (EnMS) that actually improves energy performance. We cover the PDCA backbone, energy review and significant energy uses (SEUs), setting EnPIs/EnBs, operational controls, procurement and design integration, measurement & verification, internal audits, and management review, plus practical tools, templates, and Canadian/BC context for legal and utility considerations.
This hands-on course provides the knowledge and tools to implement a Quality Management System (QMS) in alignment with ISO 9001:2015. You’ll explore the standard’s structure and principles, learn to interpret and apply its requirements, and build practical systems to manage quality performance, risks, and customer satisfaction. The course maps all activities to clauses 4 through 10 of ISO 9001, enabling participants to translate requirements into an operational QMS tailored to organizational needs.
By the end of the course, you will be able to:
Explain ISO 9001:2015 structure, key principles, and clause requirements (4–10).
Analyze the organization’s context and interested parties to define QMS scope.
Identify quality risks and opportunities and integrate them into the QMS.
Set quality objectives and KPIs aligned with strategic direction.
Establish operational processes, controls, and documented procedures.
Define roles, responsibilities, and support mechanisms (competence, awareness, communication).
Build internal audit, management review, and corrective action routines.
Understand the PDCA (Plan-Do-Check-Act) cycle within the QMS framework.
Prepare a step-by-step roadmap for ISO 9001:2015 implementation.
Collect evidence to demonstrate conformity and certification readiness.
Quality Managers and QMS Coordinators
Operations Managers and Department Heads
Internal Auditors and Compliance Officers
Process Owners and Document Controllers
Consultants supporting ISO 9001 implementations
Any staff involved in QMS development, implementation, or transition
Familiarity with your organization’s processes and structure
No prior ISO experience required
Understanding of basic process and performance metrics is helpful
ACS Academy is a federally registered Canadian provider of training and consulting services, offering accredited certificate programs, industry-focused training, and support for management systems and international standards. Backed by experienced professionals with hands-on expertise, ACS Academy delivers practical, high-quality solutions that help organizations achieve compliance, operational excellence, and sustainable growth across industries.